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Configure Tracks on UCSC Genome Browser: Human Dec. 2013 (GRCh38/hg38)
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-   MethBase2    
Human methylome studies Human methylome studies
     SRP304130     Impact of exposures to persistent endocrine disrupting compounds on the sperm methylome in regions associated with neurodevelopmental disorders [Sperm]
     SRP302514     Integrative multiplatform molecular profiling of human colorectal cancer reveals proteogenomic alterations underlying mitochondrial inactivation [The normal adjacent colorectal mucosa was obtained at a distance of 5 cm from the tumor., The normal adjacent colorectal mucosa was obtained at a distance of 6 cm from the tumor., The normal adjacent colorectal mucosa was obtained at a distance of 7 cm from the tumor., Tumor Tissue]
     SRP056911     DNA methylation in the placentas of typically developing and autistic children [Placenta]
     SRP299418     cell-free DNA sequencing of plasma [Plasma]
     SRP298508     Alternative splicing and the epigenome in CML remission [WGBS] [PBMC]
     SRP298022     DNA hydroxymethylation analysis for target regions in human smooth muscle cells. [Cultured Smooth Muscle]
     SRP298020     DNA methylation analysis for target regions in human smooth muscle cells. [Cultured Smooth Muscle]
     SRP293255     DNA Methylation Potential Energy Landscape Analysis of Pediatric Pre-B cell Acute Lymphoblastic Leukemia (ALL) and Normal B cells and precursors [Cell Line, Primary]
     SRP047086     A public-private-academic consortium, Genome-in-a-Bottle (GIAB), hosted by NIST to develop reference materials and standards for clinical sequencing [B-Lymphocyte]
     SRP193431     Early detection of lung cancer by deep methylation sequencing of circulating tumor DNA [Plasma]
     SRP286409     H3K27me3 shapes DNA methylome by inhibiting UHRF1-mediated H3 ubiquitination [Bisulfite-seq] [E14, HeLa]
     SRP286271     Homo sapiens Raw sequence reads [Cervical, Cervical Cancer, Cervical Cancer Adjacent]
     SRP286180     Comprehensive methylome sequencing reveals prognostic epigenetic biomarkers for prostate cancer mortality [Adjacent Normal, Tumor]
     SRP282493     DNA methylation maintains integrity of higher order genome architecture (WGBS) [Colorectal]
     SRP278588     DNA methyation of intragenic CpG islands are required for differentiation from iPSC to NPC [Induced Pluripotent Stem Cell, Induced Pluripotent Stem Cell Derived]
     SRP278376     Epigenetic Landscape of Pediatric Ependymoma Recurrence [Brain]
     SRP266653     TNF induced inflammatory transcription dynamics and epigenetic changes [293, HEK 293 transfected with reporter construct, RELA-KO for HEK 293 transfected with reporter construct, TET2 KO for HEK 293 transfected with reporter construct]
     SRP055494     BLUEPRINT methylome of the HapMap cell line GM18507 (Coriell cell line NA18507) [modified B cell (lymphoblastoid)]
     SRP273813     Whole genome methylation sequencing of circulating tumor cells (CTCs) in Lung cancer. [Adjacent Normal Tissue, Blood, Lung]
     SRP272635     Decoding dynamic epigenetic landscapes in human oocytes using single-cell multi-omics sequencing [Somatic]
     SRP272595     WGBS analysis of various colon cancer cell lines [Colorectal Adenocarcinoma]
     SRP272481     GATA transcription factors, SOX17 and TFAP2C, drive the human germ-cell specification program [Bisulfite-Seq] [iPSC]
     SRP271639     Cell-free DNA Methylation and Transcriptomic Signature Prediction of Pregnancies with Adverse Outcomes [WGBS] [Plasma]
     SRP269389     Targeted intragenic demethylation initiates chromatin rewiring for gene activation [HCC cell line]
     SRP268783     Acute depletion of CTCF rewires genome-wide chromatin accessibility [B Lineage Acute Lymphoblastic Leukemia SEM cell carrying bi-allelic miniAID-mClover3 knockin tags]
     SRP267967     Characterization of universal features of partially methylated domains across tissues and species [Breast Tumor, Lung]
     SRP267867     Human ribosomal DNA (rDNA) epigenetic clock [Blood]
     SRP057098     A Unique Gene Regulatory Network Resets the Human Germline Epigenome for Development [Gonad]
     SRP052842     Pleiotropic Analysis of Lung Cancer and Blood Triglycerides [purified AT2]
     SRP266759     DNA methylation repels binding of hypoxia-inducible transcription factors to maintain tumour immunotolerance [BS] [MCF7, SK-MEL-28]
     SRP266187     Non-CG methylation and multiple epigenetic layers associate child abuse with immune and small GTPase dysregulation [Lateral Amygdala (human brain tissue)]
     SRP265926     2-hydroxyglutarate drives whole-genome hypermethylation in kidney cancer cells with inactivated VHL [Cell Line, VHL inactivated clone12, VHL inactivated clone30, VHL inactivated clone44, clone12 exogenous wildtype VHL reintroduced, clone30 exogenous wildtype VHL reintroduced, clone44 exogenous wildtype VHL reintroduced]
     SRP261643     Comprehensive epigenomic profiling of human alveolar epithelial differentiation identifies key epigenetic states and transcription factor co-regulatory networks for maintenance of distal lung identity [In vitro differentiated AT1-like, purified primary AT2]
     SRP261501     Tissue-Biased Expansion of DNMT3A-Mutant Clones Associated with Conserved Epigenetic Alterations [Umbilical Cord]
     SRP260840     Naïve human embryonic stem cells can give rise to cells with trophoblast-like transcriptome and methylome [Bisulfite-Seq] [ESC, Transdifferentiated Human Trophoblast Stem Cell, Trophoblast Stem Cell]
     SRP259369     Epigenome Dysregulation Resulting from NSD1 mutation in Head and Neck Squamous Cell Carcinoma [Patient-derived head and neck squamous cell carcinoma cell line]
     SRP259185     Multi-omics analysis reveals divergent epigenetic regulation of gene expression and drivers of esophageal squamous cell carcinoma (WGBS) [Adjacent Normal Esophageal, Esophageal Squamouse Carcinoma]
     SRP051367     Bacterial Infection Remodels the DNA Methylation Landscape of Human Dendritic Cells (TAB-Seq) [Monocyte-derived dendritic]
     SRP051366     Bacterial Infection Remodels the DNA Methylation Landscape of Human Dendritic Cells (Bisulfite-Seq) [Monocyte-derived dendritic]
     SRP254660     H3K27M in Gliomas Causes a One-step Decrease in H3K27 Methylation and Reduced Spreading Within the Constraints of H3K36 Methylation [WGBS] [Cell Line]
     SRP253922     Long-term expansion with germline potential of human primordial germ cell-like cells in vitro [Bisulfite-seq] [Ovary, iPSC]
     SRP253848     LiBis: An ultrasensitive alignment method for low-input bisulfite sequencing [Blood, Tumor]
     SRP251688     Signalling networks constructed by integrative analysis of multi-omics in peripheral blood mononuclear cells in systemic lupus erythematous patients [PBMC]
     SRP250803     Genome-wide R-loop landscapes during epigenetic programming and reprogramming [ESC, Induced Pluripotent Stem Cell, Mesenchymal Stem Cell, Neural Stem Cell, Vascular Endothelial, Vascular Smooth Muscle]
     SRP246939     Beta cell-specific CD8+ T cells maintain stem-cell memory-associated epigenetic programs during type 1 diabetes (WGBS) [HAART HIV TN CD8 T cells, Polyclonal Naive CD8 T cell HD, Polyclonal T1D Naive CD8 T cells, Polyclonal TCM CD8 T cells, Polyclonal TEM CD8 T cells, Polyclonal TSCM CD8 T cells, Tetramer+ CD8 T cells, Tetramer+ HAART CD8 T cells, Tetramer+ T1D CD8 T cells]
     SRP049985     Whole Genome Bisulfite Sequencing (WGBS) of cKIT+ sorted cells from 57-137 day old fetal testes and ovaries. [cKIT+ FACS sort]
     SRP049710     Loss of 5-hydroxymethylcytosine is linked to gene body hypermethylation in kidney cancer [Matched Normal, Tumor]
     SRP049936     DNA methylation in mammalian placentas [Cerebrum, Cord Blood, Extraembryonic Membrane, Placenta, Trophoblasts]
     SRP049782     Targeted disruption of DNMT1, 3A and 3B in human embryonic stem cells [WGBS] [ES]
     SRP239226     Principles of Signalling Pathway Modulation for Enhancing Human Naïve Pluripotency Induction [WGBS] [ESC]
     SRP238023     Reliable tumor detection using cerebrospinal fluid cell-free DNA methylomes in pediatric medulloblastoma [Blast, Cerebellum, Tumor Tissue, cerebrospnial fluid from Hydrocephalus patient]
     SRP237955     Molecular atlas of fetal and adult human liver sinusoidal endothelial cells: a F8 secreting cell [methylation III] [Hepatic Sinusoidal Endothelial]
     SRP230221     Chromatin dynamics reveal circadian control of human in vitro islet maturation [WGBS] [Primary Adult Alpha, Primary Adult Beta, hPSC-derived beta, hPSC-derived definitive endoderm, hPSC-derived endocrine progenitor, hPSC-derived pancreatic progenitor 1, hPSC-derived pancreatic progenitor 2, hPSC-derived poly-hormonal]
     SRP048896     Genome-wide profiling of the DNA methylation landscape at base-pair resolution in human acute myeloid leukemia cell lines. [AML]
     SRP048844     Genome-wide profiling of DNA methylation at single-base resolution based on MeDIP-bisulfite high-throughput sequencing and ridge regression (MethyC + MeDIP) [Ovarian Epithelial]
     SRP048761     Dissecting neural differentiation regulatory networks through epigenetic footprinting [ES-derived neural progenitor]
     SRP233253     Comparison of EM-seq and WGBS results [B-Lymphocyte, Lung, Plasma]
     SRP230793     Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes [Cord Blood]
     SRP230618     Differential DNA methylation profiles of HS ILAE type 1 in human temporal lobe epilepsy [Brain Hippocampus]
     SRP229996     Stem and effector CD8 T-cells from human cancers [Blood, Kidney Tumor]
     SRP226234     An ExtendedCulture System that Supports Human Primordial Germ Cell-Like Cells Survival and Initiation of DNA Methylation Erasure [ESC]
     SRP224808     Whole genome bisulfite sequencing of human spermatozoa reveals differentially methylated patterns from type 2 diabetic patients [Semen]
     SRP045902     Resetting Transcription Factor Control Circuitry Towards Ground State Pluripotency In Human [ESC]
     SRP223055     Tibetan humans Raw sequence reads [Blood]
     SRP223612     Whole Genome Bisulfite sequencing: Allele-specific DNA methylation is increased in cancers and its dense mapping in normal plus neoplastic cells increases the yield of disease-associated regulatory SNPs [Bladder Cell Line, Blood, Bone Marrow, Brain, Breast (Primary Tissue), Breast Cell Line, Cell Line, Liver, Lymph Node, Placenta, Placenta Maternal]
     SRP221227     Persistent epigenetic memory impedes rescue of the telomeric phenotype in human ICF iPSCs following DNMT3B correction [iPSC]
     SRP220230     Human, Chimpanzee, Gorilla, Orangutan, Macaque Epigenomics [LCL]
     SRP220467     Human embryonic stem cell-derived organoidal retinoblastoma reveals cancerous origin and therapeutic target [Retina, Tumor]
     SRP219798     Regulation of DNA Methylation at Enhancers by TET2 Finetunes Gene Transcription in ERa-Positive Breast Cancer Cells [MCF7]
     SRP045269     Global loss of DNA methylation uncovers intronic enhancers in genes [Colorectal Cancer Cell Line]
     SRP217135     Systematic evaluation of library preparation methods and sequencing platforms for high-throughput whole genome bisulfite sequencing [WGBS] [Blood, White Blood]
     SRP217139     Lactate mediated epigenetic reprogramming during cancer associated fibroblast formation [CAF, MSC]
     SRP215940     The DNA methylomes of hyper-IgM syndrome type 2 B cells provide insights into the roles of activation-induced deaminase prior to the germinal center reaction [Non-Class-Switched Memory B Cells, naive B cell]
     SRP213665     The strand-biased mitochondrial DNA methylome and its regulation by DNMT3A [HEK293T_WGBS] [HEK293T]
     SRP213117     Single-cell transcriptome analysis of uniparental embryos reveals parent-of-origin effects on human preimplantation development [methylation] [Embryo]
     SRP043461     The effects of the global loss of DNA methylation on the functional cancer epigenome (Bisulfite-seq) [DKO1, HCT116]
     SRP198282     Hammer-seq to measure kinetics of DNA methylation maintenance in HeLa cells [Cervix, Inner Cell Mass]
     SRP199200     CATACOMB: an endogenous inducible gene that antagonizes H3K27 methylation activity of Polycomb Repressive complex 2 via a H3K27M-like mechanism [HEK293T]
     SRP193843     DNMT1 drives 4D genome rewiring during oncogene induced senescence [WI-38hTERT/GFP-RAF1-ER]
     SRP198624     Whole genome bisulfite sequencing of esophagus squamous cell carcinoma [Esophagus]
     SRP194341     Whole-exome, transcriptome and epigenome data for homo sapiens from normal to dysplasia to colorectal cancer [Colon]
     SRP021039     Selective demethylation and altered gene expression are associated with ICF Syndrome in human induced pluripotent stem cells and mesenchymal stem cells [Induced Pluripotent Stem Cell]
     SRP065930     HX1 [Blood]
     SRP193115     ATAC-Me captures spatiotemporal dynamics of DNA methylation across the chromatin accessible genome [THP-1 Monocyte]
     SRP192966     Gene expression, methylome and splicing of THP-1 monocytic cells and THP-1-derived macrophage [Monocytic Cell Line]
     SRP028804     The DNA methylation landscape of human early embryos [Embryo]
     SRP187153     Comparison of methylome data generated with HiSeq X Ten and NovaSeq [IMR90]
     SRP041984     Epigenetic and transcriptional aberrations in human pluripotent stem cells reflect differences in reprogramming mechanisms [Fibroblast, Pluripotent]
     SRP186642     Genome-wide methyl-cytosine competition by DNMT and TET [ESC, EpiSCs, In Vitro Derived Motor Neurons]
     SRP041828     Comparison of nucleosome occupancy and chromatin states between normal and cancer cell lines [HMEC, MCF7, PC3, PrEC]
     SRP041822     Methylation QTLs are associated with coordinated changes in transcription factor binding, histone modifications, and gene expression levels [Bisulfite-Seq] [Lymphoblastoid Cell Line]
     SRP186275     Bisulfite-seq profiling of the human neutrophil genome during PMA- and E. coli encounter-induced activation [Blood]
     SRP186015     Study of DNA methylation pattern in single basepair resolution in the human dopaminergic neurons [LUHMES-derived neurons]
     SRP185639     DNMT3B has oncogenic activity but evidence suggests that it does not promote CIMP nor cooperate with activated BRAFV600E in human intestinal cancer. (WGBS) [Fetal Lung Fibroblasts]
     SRP041720     Genome-wide profiling of the DNA methylation landscape at base-pair resolution in human neurological disorders (Bisulfite-Seq) [brain Grey matter]
     SRP041718     Genome-wide DNA hypomethylation and RNA:DNA hybrid accumulation in Aicardi-Goutières syndrome [Primary]
     SRP125992     Activation of neuronal genes via LINE-1 elements upon global DNA demethylation in human neural progenitors [Fetal-Derived Neural Progenitor Cells (Sai)]
     SRP175163     Loss of hydroxymethylcytosine is an independent adverse prognostic factor in clear cell Renal Cell Carcinoma (ccRCC) and can be abrogated by ascorbic acid mediated TET activation [786-O]
     SRP174219     Replication timing and epigenome remodelling are associated with the nature of chromosomal rearrangements in cancer [Bisulfite-Seq] [Breast]
     SRP041025     WGBS data of pediatric B-cell acute leukemias [Bone Marrow / Peripheral Blood]
     SRP170543     Impaired DNA methylation in oocytes with a mutation in KHDC3L causing recurrent hydatidiform mole [embryo day 6]
     SRP168427     Tet inactivation disrupts YY1 binding and long-range chromatin interactions to cause developmental defects in embryonic heart [Embryonic Heart]
     SRP167041     Homo sapiens Epigenomics [Breast, Plasma]
     SRP163251     Rates of acquisition of de novo mutations in human pluripotent stem cells under different culture conditions [PSC]
     SRP162996     Very long intergenic non-coding RNA transcripts and expression profiles are associated to specific childhood acute lymphoblastic leukemia subtypes [CD10+ CD19+ Cord blood, Pre-B t(12 21) [ETV6-RUNX1] acute lymphoblastic leukemia]
     SRP038103     Genome-wide methylation maps for untreated and Aza treated AML3 cells [AML3]
     SRP037971     Genome wide profiling of MBD2 binding [MCF-7 WT]
     SRP161783     Whole Genome Bisulfite Sequencing of Rett Syndrome and Control Human BA9 Cortex [Brain]
     SRP161745     Human retinal pigment epithelium [Cultured Retinal Pigment Epithelum, Eye]
     SRP158940     N6-methyladenine DNA Modification in Glioblastoma [ChIP-seq, BiSulfite-seq, DIP-seq] [Blast]
     SRP158895     Comparison of methylome data obtained with rPBAT and tPBAT. [Lung]
     SRP158894     Optimization of the input amount of library for whole-genome bisulfite sequencing on HiSeq X Ten [Lung]
     SRP158409     H3K36me2 recruits DNMT3A and shapes intergenic DNA methylation landscapes [C3H embryo-derived mesenchymal progenitor, C57BL/6 x 129S4/SvJae F1 embryo-derived ESCs, Patient-derived head and neck squamous cell carcinoma cell line]
     SRP158279     Epigenetic reprogramming at estrogen-receptor binding sites alters the 3D chromatin landscape in endocrine resistant breast cancer [WGBS] [Breast Cancer]
     SRP156136     MethMotif: An integrative cell specific database of transcription factor binding motifs coupled with DNA methylation profiles [Colon, Spleen]
     SRP035642     The relationship between DNA methylation, genetic and expression inter-individual variation in untransformed human fibroblasts [Whole genome bisulfite sequencing] [Blast]
     SRP155006     Epigenomic signatures in liver and blood of Wilson disease patients include hypermethylation of liver-specific enhancers [Blood, Liver]
     SRP151496     Generation of FOXO3 engineered human stem cells with enhanced efficacy and safety [ECs, MSCs, TransMSCs, VSMCs]
     SRP136499     A genomic study of the contribution of DNA methylation to regulatory evolution in primates [Heart, Heart (Later Reclassified As Liver), Kidney, Liver, Lung]
     SRP148683     Comparison of transcriptome profiles of human embryo cultured in either closed or standard incubator [Preimplantation Embryo]
     SRP126139     G-quadruplex structures moulds the DNA methylome [Cell Line]
     SRP144312     Widespread transposable element-driven oncogene expression in cancers [Lung Cancer Cell Line]
     SRP144098     DNMT3B maintains mCA landscape and regulates mCG status of bivalent promoters in human embryonic stem cells [ESC]
     SRP117084     Transcription elongation regulates genome 3D structure [monocyte derived macrophages (MDM)]
     SRP033504     Epigenome analysis of human epidermal samples with aging and sun exposure [Dermis]
     SRP033491     China_type_2_diebetes_family
     SRP033283     The RON receptor tyrosine kinase promotes metastasis by triggering epigenetic reprogramming through the thymine glycosylase MBD4 (Bisulfite-Seq) [Breast Cancer Cell Line]
     SRP033252     Genome-wide profiling of the functional DNA methylation landscape at base-pair resolution in human cancer types [BS-seq] [Blood (B-cells), Brain, Brain (grey matter), Brain (white matter), Breast, Colon, Liver, Lung, Placenta, Prostate]
     SRP033201     Homo sapiens Genome sequencing
     SRP133999     Developmental origins define epigenomic differences between subcutaneous and visceral adipocytes [Bisulfite-Seq] [Blood, Subcutaneous Adipose, Visceral Adipose]
     SRP133941     Longitudinal Personal DNA Methylome Dynamics in a Human with a Chronic Condition [PBMC]
     SRP133910     Homo sapiens Raw sequence reads [Blood]
     SRP032354     whole-genome bisulfite sequencing (BS-seq) of HEK293 cells (HEK293-CT) and HEK293 cells stably over-expressing the BAHD1 gene (HEK-BAHD1) [Embryonic Semi-Differentiated Kidley, modified HEK293 cell overexpressing BAHD1]
     SRP132785     Active BRAF-V600E is the key player in generation of a sessile serrated polyp-specific DNA methylation profile (WGBS data set) [Blood, Colon]
     SRP132292     Genetic determinants and epigenetic effects of pioneer factor binding [WGBS] [immortalized BJ foreskin fibroblast cell line]
     SRP131900     Lymphocyte-specific chromatin accessibility pre-determines glucocorticoid resistance in acute lymphoblastic leukemia [WGBS] [ALL xenograft cells]
     SRP131790     Whole Genome Bisulfite Sequencing of Autism and Control Human BA9 Cortex [Dorsal Lateral Prefrontal Cortex]
     SRP131112     Endurance training remodels sperm-borne small RNA expression and methylation at neurological gene hotspots [RRBS] [Motile Semen]
     SRP131087     An epigenomic approach to identifying differential overlapping and cis-acting lncRNAs in cisplatin-resistant cancer cells [BiSulfite-seq] [Lung, Ovarian]
     SRP130992     Genome-wide Methylation in Cordblood CD4+ Cells from Newborns Exposed vs. Unexposed to Maternal Tobacco Smoke During Pregnancy [Cord blood CD4+]
     SRP130768     Homo sapiens bisulfite and mRNA sequencing of blood T cells and LCM collected lung cells [Blood, Lung]
     SRP128919     DNA methylation in hESC derived brain organoids and iPSC derived neurons, astrocytes and neural progenitors [Whole Organoid]
     SRP127667     Epigenetic marks and nuclear transcriptomes of cardiac myocytes [Heart Left Ventricle]
     SRP127273     Scalable and efficient single-cell DNA methylation sequencing by combinatorial indexing. [Embryonic Kidney Blood Skin]
     SRP126972     Distinct Epigenetic Subtypes Are Linked to Disease Progression in Low-Risk MDS [Peripheral blood (PB)]
     SRP126677     Genome-wide profiling at single-nucleotide resolution of brain cell types in schizophrenia [WGBS] [Brain]
     SRP029519     Induction of sarcomas by mutant IDH2 [10T isogenic cell line with IDH2 mutation]
     SRP125973     A modular dCas9-SunTag DNMT3A epigenome editing system overcomes pervasive off-target activity of direct fusion dCas9-DNMT3A constructs [Cervical Cancer Cell Line]
     SRP125826     Intervals of unmethylated DNA spatially co-segregate in cis and in trans [WGBS] [Erythroid Progenitor Cells]
     SRP028600     Charting a dynamic DNA methylation landscape of the human genome [Cell Line, Cortex, Normal, Primary Tumor, Tumor Tissue]
     SRP028577     Large-scale hypomethylated blocks associated with Epstein-Barr virus-induced B-cell immortalization [Bisulfite-seq] [Activated B-cells, Activated B-cells day 16, Activated B-cells week 3, EBV transformed B-cells, EBV transformed B-cells 16 days post infection, EBV transformed B-cells 3 weeks post infection, Resting B-cells]
     SRP113417     Chromatin and Transcriptional Dynamics in Adult Germline Stem Cells and Mammalian Spermatogenesis [Spermatogonia (Thy1+), Testis]
     SRP119706     DNA hypermethylation encroachment at CpG island borders in cancer is predisposed by H3K4 monomethylation [WGBS_Hs] [Adjacent Benign Normal Prostate, Prostate Tumor]
     SRP678403     Homo sapiens Genome sequencing and assembly [Brain, Dermis, Epidermis, Heart, Kidney, Lung, Muscle]
     SRP026604     Genome-wide methylation maps for Proliferating and Senescent cells [IMR90]
     SRP117159     Homo sapiens cultivar:PLC/PRF/5 Raw sequence reads [Liver]
     SRP074598     Single Cell DNA Methylome Sequencing of Human Preimplantation Embryos [Heart, ICM, Sperm, TE, Villus]
     SRP116948     Whole genome bisulphite sequencing using the Illumina X system [Bisulfite-Seq] [EBV-transformed lymphoblastoid cell line, Fetal Lung Fibroblast]
     SRP124518     UBE3A-mediated regulation of imprinted genes and epigenome-wide marks in human neurons [Neuronal Cell Line, chromosome duplication model of Dup15q syndrome]
     SRP645487     Embryonic stem cell factors DPPA2/4 amplify active H3K4me3-H2AK119ub chromatin domains in non-small cell lung cancer (BS-seq) [Lung Cancer, Ovarian Cancer]
     SRP643149     WGBS data from a DNA dilution series (K562 in NA12878 background) with pUC19 and Lambda spike-in controls.
     SRP641668     Non-classical epigenome rewiring and its genetic determinants as a cause of cellular senescence and aging-related diseases [Umbilical Vein Endothelium]
     SRP636882     Chamber-Specific Chromatin Architecture Guides Functional Interpretation of Disease-Associated Cis-Regulatory Elements in Human Cardiomyocytes [Heart Left Atria]
     SRP115074     Lack of Repressive Capacity of Human Promoter DNA Methylation identified through Genome-Wide Epigenomic Manipulation [Brest Cancer Cell Line]
     SRP026048     Global epigenomic reconfiguration during mammalian brain development [Brain (Cerebral Cortex), Brain (Dorsal Prefrontal Cortex), Brain (Frontal Cortex), Brain (Middle Frontal Gyrus), ESC]
     SRP616697     Integrated epigenetic and genetic programming of primary human T cells [WGBS] [Bulk T cells]
     SRP610863     Generating Revitalized Stem Cell-Engineered CAR-NKT Cells for the Treatment of Malignant Pleural Mesothelioma [HSPC-cell, PBMC15MCAR-NKT]
     SRP596512     Disordered DNA methylation leads to targetable transcriptional plasticity in ATRT [WGBS cell line] [Cell Line]
     SRP596170     Chemical reprogramming of human blood cells into hCiPS cells [ADSC derived hCiPSC, EPC derived hCiPSC]
     SRP593822     Memory-like T cells emerge early in circulation after gene therapy for SCID-X1 [Bisulfite-Seq] [Blood]
     SRP518400     Enriched Methylome [Bone Marrow]
     SRP588774     Three Dimensional Matrigel Endows Human Formative Pluripotent Stem Cells with Pre-gastrula Stage Epiblast Features [WGBS]
     SRP580181     Dynamic Multi-omics Profiling Unveils Bimodal Epigenetic Roles of Chromatin O-GlcNAc modification in Premature Senescence Program [BiSulfite-seq] [Primary Fibroblasts]
     SRP107883     Archaic and modern bone DNA methylation maps from the Neanderthal, Denisovan, modern human and chimpanzee [Bone]
     SRP107857     TRIM28-Regulated Transposon Repression Is Required for Human Germline Competency and Not Primed or Naive Human Pluripotency [naive ESC, primed ESC]
     SRP577515     DNA methylation changes in Tatton-Brown-Rahman Syndrome models of neuronal development [D-IN, V-IN, V-Npc, iGlut]
     SRP576746     CD19-CAR T cells undergo exhaustion epigenetic programming in patients with acute lymphoblastic leukemia [CD8+ T Cells]
     SRP574020     Silencing TET1 expression alters the epigenomic landscape and amplifies transcriptomic responses to allergen in airway epithelial cells [Bronchial Epithelial]
     SRP571369     Genome-wide DNA methylation profiling of human CD4+ T helper cells define epigenetic signatures for Th1, Th17 and non-classic Th1 cells [Blood, Culture]
     SRP106910     Human memory CD8 T-cell effector-potential is epigenetically preserved during in vivo homeostasis [HuTCM, HuTEM, HuTN, HuTSCM, TCMD204, TEMD203, TND201, TSD202]
     SRP568118     High-Fidelity, Efficient Human Post-Implantation Embryo Models Generated by STAT3-Induced Cell Plasticity [WGBS] [Pluripotent Stem Cell]
     SRP022182     Homo sapiens Epigenomics
     SRP022160     Whole-genome analysis of 5-hydroxymethylcytosines and 5-methylcytosines at base resolution in human brain [Brain Prefrontal Cortex]
     SRP022149     Genome-wide parent-of-origin DNA methylation analysis [Methyl-seq] [Normal Brain, Normal Liver, Normal Placenta]
     SRP104789     Culture of Human embryonic stem cells in different media [ESC]
     SRP104305     5hmC dynamically correlated with enhancer''s activities during hES-to-Pancreatic endoderm cell differentiation (Bisulfite-Seq) [ESC]
     SRP559414     The myoblast methylome: Multiple types of associations with chromatin and transcription [Skeletal Muscle]
     SRP104141     NicE-seq: high resolution open chromatin profiling [Colorectal]
     SRP103943     DNA epigenome editing using CRISPR-Cas SunTag-directed DNMT3A [WGBS] [epithelial HEK 293T cells]
     SRP103839     Single-cell Multi-omics Sequencing and Analyses of Human Colorectal Cancer [CRC, HeLa contaminant]
     SRP022041     Buccals are likely to be a more informative surrogate tissue than blood for epigenome-wide association studies [Bisulfite-Seq] [Buccal]
     SRP103794     Methylation DNA mediated KLF4 binding activity in glioblastoma cells [Brain]
     SRP555335     Genome-wide methylation sequencing data (WGBS) from 10 urothelial carcinoma and matched normal tissues [Bladder]
     SRP021846     Age-related methylation changes are associated with altered transcriptional circuitry [Methyl-seq] [Skin (Epidermal Suction Blister Samples)]
     SRP021479     Genome-wide DNA methylation aberrations in human atherosclerosis (sequencing) [Carotid]
     SRP103077     Mapping DNA methylation and CTCF/cohesin occupancy on nascent chromatin and DNMT-targeted nascent chromatin [ESC]
     SRP551562     DNA Methylation Profiling at Base-Pair Resolution Reveals Unique Epigenetic Features of Early-Onset Colorectal Cancer in Underrepresented Populations [Moderately Differentiated Rectal Adenocarcinoma, Moderately Differentiated Rectosigmoid Adenocarcinoma, Moderately Differentiated Sigmoid Colon Cancer, Normal Adjacent Colonic Mucosal, Normal Adjacent Rectal, Normal Adjacent Rectosigmoid, Normal Adjacent Sigmoid, Rectal Adenocarcinoma Arising From Tubulovillous Adenoma With High Grade Dysplasia]
     SRP551395     Clonorchis sinensis infection alters the methylation and hydroxymethylation of hepatocellular carcinoma [HCC adjacent, HCC tumor]
     SRP102997     Genome-wide nucleosome occupancy and DNA methylation profiling in endometriosis cells [hTERT immortalized endometriosis]
     SRP543819     Seminal Plasma cell-free DNA [Seminal Plasma]
     SRP541825     Intragenic Epigenetic Deregulation by IDH2 Mutations Synergizes with SRSF2 Mutations Causing Mis-splicing of Key Transcriptional Regulators [BiSulfite-seq] [Blood, Marrow]
     SRP101887     Neuronal brain region-specific DNA methylation and chromatin accessibility are associated with neuropsychiatric trait heritability [Bisulfite-Seq] [anterior cingulate cortex (BA24), hippocampus (HC), nucleus accumbens (NAcc), prefrontal cortex (BA9)]
     SRP536371     DNA methylation protects cancer cells against non-canonical senescence [Colon]
     SRP338680     Molecular profile of HepG2 cell line (IBMC) [Liver]
     SRP533334     Methylation patterns of the nasal epigenome of hospitalized SARS-CoV-2 positive patients reveal insights into molecular mechanisms of COVID-19 [Nasopharyngeal Swab]
     SRP531388     Inferring DNA methylation in non-skeletal tissues of ancient specimens [Bone (Femur)]
     SRP528679     The Recombinase RAD51 Plays Critical Roles in the Maintenance Methylation of Genomic DNA by Promoting DNMT1 Stability and Recruitment [HCT116]
     SRP527234     Induction of meiosis from human pluripotent stem cells [Bisulfite-seq] [day10, day15, day2, day5, hiPSC]
     SRP526881     Total plasma cfDNA methylation in kidney transplant recipients provides insight into acute allograft rejection pathophysiology [Plasma]
     SRP526064     Valine-restricted diet regulates DNA methylation [Bisulfite-Seq] [HCT116]
     SRP100067     Epigenome-wide analysis of DNA methylation in lung tissue shows concordance with blood studies and identifies tobacco smoke-inducible enhancers [purified primary alveolar epithelial type 2]
     SRP525370     Bulk whole genome bisulfite sequencing from benign human Fallopian tube [Fallopian Tube]
     SRP525209     Methylation changes induced by alpha-hemolysin from Staphylococcus aureus in human primary Th1 lymphocytes [Lymphocyte]
     SRP099603     Enrichment methods provide a feasible approach to comprehensive and adequately powered investigations of the methylome [Postmortem Brain]
     SRP523753     Vitamin C promotes epidermal proliferation by enhancing the DNA demethylation of proliferation-related genes in human epidermal equivalents (WGBS) [Epidermal Equivalent]
     SRP523710     Rapid Human Oogonia-like Cell Specification via Combinatorial Transcription Factor-Directed Differentiation [BiSulfite-seq] [DDX4+ induced oogonia-like, DDX4+ induced oogonia-like cells (no DNMT1i), DDX4+ induced oogonia-like cells naive reset, PGCLC, hiPSC naivereset, hiPSC primed]
     SRP521389     Bisulfite-Free Whole-Genome Mapping of 5-Methylcytosine at Single-Base Resolution by TAD-seq [Cell Line]
     SRP521100     Continuous turnover and asynchronous aging of human memory T cells across tissues [Jejunum, Lung, Mesenteric Lymph Node, Spleen]
     SRP098648     Comprehensive evaluation of genome-wide 5-hydroxymethylcytosine profiling approaches in human DNA [BiSulfite-seq] [Adult Brain Frontal Lobe, LNCaP clone]
     SRP519334     sciMETv3 Single-cell DNA Methylation Raw Sequence Reads [BA46]
     SRP097759     S-adenosylhomocysteine hydrolase participates in DNA methylation inheritance [Kidney]
     SRP516302     Modulating immune cell fate and inflammation through CRISPR-mediated DNA methylation editing [WGBS-seq] [B-ALL cell line]
     SRP510797     Homo sapiens Raw sequence reads [Kidney]
     SRP515825     Mitochondria-localized MBD2c facilitates mtDNA transcription and drug resistance [Bisulfite-Seq] [MDA-MB-468]
     SRP515320     Epigenetic dysregulation of transposable elements in cognitive impairment and Alzheimer's disease [Isolated WBC]
     SRP478956     Divergent originations of parental DNA hydroxymethylation in human preimplantation embryos [ESC]
     SRP514328     DNA 5-methylcytosine regulates genome-wide formation of G-quadruplex structures [WGBS] [Embryonic Kidney]
     SRP019232     Whole genome bisulfite-seq of two healthy males. [Hair Follicle, Peripheral Blood Lymphocyte]
     SRP001371     University of Washington Human Reference Epigenome Mapping Project [Fetal Intestine Large, Fetal Intestine Small]
     SRP511776     Patient TSC2 Mutant Cells Exhibit Aberrations in Early Neurodevelopment Accompanied by Changes in the DNA Methylome (Bisulfite-Seq) [iPSC-derived neural progenitor, induced pluripotent stem cells (iPSC)]
     SRP511377     Bisulfite seq of UHRF1 KO A549 cells [Tumor]
     SRP510877     High-Resolution Molecular Profiling of Epileptic Brain Activity via Explanted Depth Electrodes [Methylation] [Brain]
     SRP510686     A comparison of methylome data produced with tPBAT and sPBAT library preparation protocols. [IMR-90 (JCRB9054)]
     SRP510440     Tracking and mitigating imprint erasure during induction of naïve human pluripotency at single-cell resolution [Bisulfite-Seq] [ESC]
     SRP096028     Dental Pulp Stem Cells Model Early Life and Imprinted DNA Methylation Patterns. [Dental Pulp Stem Cell, Luhmes]
     SRP508090     Epigenomic landscape of human cumulus cells in premature ovarian insufficiency using single-base resolution methylome and hydroxymethylome. [scWGBS_seq] [Ovary]
     SRP504847     Ectopic expression of DNMT3L in human trophoblast stem cells restores features of the placental methylome [PBAT BS-Seq] [Trophoblast Stem Cell]
     SRP504674     Generation of human spermatogonia from pluripotent stem cells [PGCLC, xrTestis]
     SRP504106     Mutant IDH1 inhibition induces reverse transcriptase and dsDNA sensing to activate tumor immunity [human WGBS] [Cholangiocarcinoma]
     SRP503688     Genome-wide DNA methylation seq data and RNA seq data in three paired HCC and normal tissue samples [HCC, Paracancerous]
     SRP501436     Transcriptomic and epigenomic consequences of heterozygous loss-of-function mutations in AKAP11, a shared risk gene for bipolar disorder and schizophrenia [WGBS] [iPSCs were derived from lymphoblasts]
     SRP500704     Bisulfite-Free Whole-Genome Mapping of 5-Methylcytosine at Single-Base Resolution by NTD-seq [Cell Line]
     SRP095006     Genome-wide determination of on-target and off-target characteristics for RNA-guided DNA Methylation by dCas9 methyltransferases (CRISPRme) [WGBS] [Embryonic Kidney Cell Line]
     SRP094960     Genomic profiling of human spermatogonial stem cells [WGBS] [Testis]
     SRP499337     Repetitive element transcript accumulation is related to inflammaging in humans [PBMC]
     SRP498758     Molecular mechanisms of Target organ damage in youth with primary hypertension [bisulfite-Seq] [Blood]
     SRP094721     Epigenomic landscapes of hESC-derived neural rosettes [Neural Stem Cell]
     SRP496763     Charting the regulatory landscape of TP53 on transposable elements in cancer [WGBS] [A549, HCT116, RKO]
     SRP094554     A Molecular signature for Delayed Graft Function [BS-Seq] [Kidney]
     SRP434804     MECP2 directly interacts with RNA polymerase II to modulate transcription in human neurons [WGBS] [Neuron]
     SRP494617     methylGrapher: Genome-Graph-Based Processing of DNA Methylation Data from Whole Genome Bisulfite Sequencing [1000 Genomes LCL]
     SRP494242     Methylation changes induced by alpha-hemolysin from Staphylococcus aureus in human primary Th17 lymphocytes. [Lymphocyte]
     SRP491820     Cell-free DNA Methylation Patterns in Aging and Their Association with Inflamm-aging [Plasma]
     SRP093764     Epigenetic resetting of human pluripotency [ESC]
     SRP490212     UHRF1 ubiquitin ligase activity supports the maintenance of low-density CpG methylation [BiSulfite-seq] [Colorectal Carcinoma epithelial]
     SRP490076     Persistent epigenome anomalies in induced pluripotent stem cells from late-onset sporadic Alzheimer's disease cases [BiSulfite-seq] [iPSC]
     SRP093254     Whole Genome Bisulfite Sequencing of HUES8 WT and HUES8 TET1/2/3 TKO hESCs [ESC]
     SRP485412     PRC2-AgeIndex: a universal biomarker of aging and rejuvenation [WGBS] [Dermal Fibroblasts, Foreskin Fibroblasts]
     SRP092462     HUES8 TET1/2/3 TKO hESCs [ESC]
     SRP480822     Novel culture systems for naive human embryonic stem cells based on chemical molecule screening [WGBS] [Naive State, Primed State]
     SRP479947     DNMT1-Dependent PLPP3: A Novel Regulator of Ovarian Aging Through Inhibition of Oxidative Stress-Related Protein Translation [Ovary]
     SRP479666     Simultaneous Targeting of Ovarian Cancer and Its Microenvironment Using Stem Cell-Engineered Off-The-Shelf CAR-NKT Cells [MNKT, MT]
     SRP479538     H3K36me3-coupled DNA Demethylation by DNMT3A Is Essential for Hypoxia-Induced EMT of Cancer Cells [Bisulfite Sequencing] [Colon]
     SRP478896     SMCHD1 controls the structure and accessibility of heterochromatin and functions as an organizer of genome compartments [Pectoralis Major Muscle]
     SRP476462     Epigenetic enigma: reinstating normalcy at a naïve chromosomal locus by suppressing an oncogenic lncRNA transgene [Bisulfite-Seq] [Colon Origin]
     SRP473783     scNanoSeq-CUT&Tag: a long-read single-cell CUT&Tag sequencing method for efficient chromatin modification profiling within individual cells [Blood]
     SRP092113     Splinted Ligation Adapter Tagging, a novel library preparation for whole genome bisulphite sequencing [ALL cell line, Lymphoblastoid Cell Line]
     SRP474233     Identification of differentially expressed tumour-related genes regulated by UHRF1 regulated DNA methylation [WGBS] [Mammary Gland]
     SRP471363     KOREF Multiome Reference [Blood]
     SRP470181     Hypermethylation of DNA impairs megakaryogenesis in delayed platelet recovery after allogeneic hematopoietic stem cell transplantation [Bone Marrow]
     SRP467808     IN-vitro HTM sequencing Raw sequence reads [HTM, Tissue]
     SRP467414     DNA methylation profiling identifies TBKBP1 as potent amplifier of cytotoxic activity in CMV-specific human CD8+ T cells [Blood]
     SRP464400     Epigenetic signature of human vitamin D3 and IL-10-conditioned regulatory DCs [Leukapheresis Products]
     SRP464289     DNMT3B PWWP mutations cause hypermethylation of heterochromatin (WGBS) [Colorectal Cancer Cell Line]
     SRP462543     iPSC-based modeling of preeclampsia identifies defects in extravillous trophoblast differentiation [Mesenchymal Stem Cell, Placenta, iPSC derived extravillous trophoblast, iPSC derived trophoblast stem cell, iPSC reprogrammed from renal epithelial, iSPC reprogrammed from mesenchymal stem cell]
     SRP462521     A role of p53 in mediating epigenetic stress (WGBS) [Kidney Epithelial]
     SRP461724     Endogenous retrovirus LTR12C hold potential locus-dependent activities as promoter and/or enhancer [BiSulfite-seq] [Embryonic Kidney]
     SRP461642     Whole genome bisulfite sequencing identifies stage- and subtype-specific DNA methylation signatures in pancreatic cancer [Normal Pancreatic Ductal Mouse Organoid, Normal Pancreatic Ductal Patient-Derived Organoid, PanIN mouse organoid, Pancreatic Ductal Adenocarcinoma Mouse Organoid, Pancreatic Ductal Adenocarcinoma Patient-Derived Organoid]
     SRP090105     The Dynamic Epigenetic Landscape of the Retina During Development, Reprogramming, and Tumorigenesis [WGBS_Hs] [Retina]
     SRP089722     Critical evaluation of the Illumina MethylationEPIC BeadChip microarray for whole-genome DNA methylation profiling [WGBS] [primary prostate epithelial cells (PrEC), prostate cancer cell line (LNCaP)]
     SRP456983     The role of HELLS in human induced pluripotent stem cells [Cell Line]
     SRP456514     A modular dCas9-based recruitment platform for combinatorial epigenome editing [Embyonic Kidney]
     SRP454277     Characterisation and reproducibility of the HumanMethylationEPIC v2.0 BeadChip for DNA methylation profiling [WGBS] [Prostate Tumour]
     SRP453184     Viral reprogramming of host transcription initiation [B Cell Lymphoma]
     SRP452335     Epigenetic sequencing of allogeneic HSC-derived CAR-engineered NKT cells [BCAR-iNKT, BCAR-iNKT-IL15, Bcar-T]
     SRP451599     The effect of Histone H3.3 knockdown on DNA methylation in HepG2 cells [Hepatoma]
     SRP450683     Epigenomic landscape of colorectal adenoma and cancer [Colorectal]
     SRP450395     Epigenetic therapy targets the 3D epigenome in endocrine-resistant breast cancer [WGBS] [Breast cancer PDX model Gar15-13, Breast cancer PDX model HCI005]
     SRP446321     Non-canonical functions of UHRF1 maintain DNA methylation homeostasis in cancer cells [Colon]
     SRP445661     Whole-genome bisulfite sequencing (WGBS) was performed for 12 HCC and paired NATs [Liver]
     SRP386415     SELF-PATTERNING OF HUMAN STEM CELLS INTO POST-IMPLANTATION LINEAGES [Cell Line]
     SRP441209     Omics analyses of stromal cells from ACM patients reveal alterations in chromatin organization and mitochondrial homeostasis [Bisulfite-Seq] [Cardiac Mesenchymal Stromal]
     SRP441171     Single-stranded Premethylated 5mC Adapters Uncovers the Methylation Profile of Plasma Ultrashort Single-Stranded Cell-Free DNA [Plasma]
     SRP440514     TNRC18 recognizes H3K9me3 to mediate transposable elements silencing at ERV regions [WGBS] [Embryonic Kidney]
     SRP439675     NPC268 whole-genome bisulfite sequencing (WGBS) [Nasopharyngeal Carcinoma]
     SRP341621     LABS: linear amplification-based bisulfite sequencing for ultrasensitive cancer detection from cell-free DNA [Plasma Separated From Blood]
     SRP436137     Malignant Transformation Drives DNA Methylation Loss and Transcriptional Activation of Transposable Element Loci [WGBS] [Neonatal Foreskin]
     SRP082156     Cancer Associated Fibroblasts are defined by a core set of epigenome changes that contribute to the tumor phenotype [WGBS] [Prostate]
     SRP080893     Active and senescent human hematopoietic stem and progenitor cell whole genome bisulfite sequencing [DNA]
     SRP432935     Epigenetic modification sequencing data of human U2OS cells [Tibia]
     SRP080340     Evidence That Three Classes of Methylomes Specific for Stem, Somatic and Transformed Cells Are Set by Three Independent Mechanisms (Methyl-Seq) [Blast]
     SRP430982     Whole genome bisulfite sequencing data of blood cfDNA form 29 CRC and 9 Non-CRC patients. [Blood]
     SRP426633     DNA methylation alterations in prostate cancer patient derived xenograft models revealed by whole genome bisulfite sequencing [Patient Derived Xenograft]
     SRP426514     Epigenetic therapy activates TE-chimeric transcripts to provide additional source of antigens in glioblastoma stem cells [Brain, Skin]
     SRP424257     Direct enzymatic sequencing of 5-methylcytosine at single-base resolution [1] [Glioblastoma Tumor]
     SRP423445     Ultrafast Bisulfite Sequencing for Efficient and Accurate 5-Methylcytosine Detection in DNA and RNA [ESC, Plasma, Stem Cell]
     SRP420728     5-hydroxymethylcytosines regulate gene expression as a passive DNA demethylation resisting epigenetic mark in proliferative somatic cells [methylation] [HEK293T]
     SRP373598     GM12878 MultiOmics [Blood]
     SRP241842     REH MultiOmics [B Cell Precursor Leukemia]
     SRP415835     Comprehensive sequence-based DNA methylation analysis suggests that PanIN lesions are acinar-derived and epigenetically primed for carcinogenesis [Pancreas]
     SRP404930     LN-stem, tumor stem, tumor terminally differentiated CD8 T cells from human kidney cancer [LN, PBMC, Spleen, TDLN, Tumor]
     SRP076893     “Same Difference”: Comprehensive evaluation of four DNA methylation measurement platforms [Lung Fibroblast]
     SRP015742     GSE40832: Whole Genome Bisulfite Sequencing by ENCODE/HAIB [ESC, Normal]
     SRP015704     Genome-wide mapping of nucleosome positioning and DNA methylation within Individual DNA molecules [Glioblastoma, Lung Fiboblast Cells]
     SRP409096     Epigenetic dynamics during capacitation of naïve human pluripotent stem cells [PBAT] [chemically reset hPSC, conventional hPSC, embryo-derived naive hPSC]
     SRP408041     The catalytic activity of TET1 is required for human germ cell fate choice [Bisulfite-Seq] [ESC, PGCLC]
     SRP405928     Optimized bisulfite sequencing reveals the lack of 5-methylcytosine in mammalian mitochondrial DNA [WGBS] [Brain, Breast Cancer, ESC, Embryonic Kidney, Hepatocarcinoma, Lung Adenocarcinoma, Melanoma, Neuroblastoma, Platelet]
     SRP405874     Rebalancing TGFß1/BMP Signals Preserves Effector and Memory Programs in Terminally Dysfunctional CD8+ T Cells [Bisulfite-Seq] [Cord Blood]
     SRP075910     Global delay in nascent strand DNA methylation [Cell Line, ESC]
     SRP075876     Cerebral Organoids Recapitulate Epigenomic Signatures of the Human Fetal Brain [Brain, ESC]
     SRP357194     HPV integration generates cellular super enhancer and functions as ecDNA to regulate genome-wide transcription [C33A, CaSki, HeLa, S12, SiHa]
     SRP075562     ZBTB33 (Kaiso) Differentially Regulates Cell Cycle Through cyclin D1 and cyclin E1 in a Cell Specific Manner [BiSulfite-seq] [HeLa]
     SRP012412     GSE59395: Genome-wide map of regulatory interactions in the human genome [Adrenal Gland, Body Of Pancreas, Bone Marrow, Cell Line, Esophagus Muscularis Mucosa, Esophagus Squamous Epithelium, Fibroblast Of Arm, Gastroesophageal Sphincter, Heart Left Ventricle, Hepatocellular Carcinoma, Hepatocyte, Lower Leg Skin, Mammary Epithelial, Motor Neuron, Ovary, Prostate Gland, Right Lobe Of Liver, Smooth Muscle, Spleen, Stomach, Suprapubic Skin, Testis, Thyroid Gland, Tibial Nerve, Transverse Colon, Upper Lobe Of Left Lung]
     SRP014898     Human Sperm Epigenomes and Transcriptomes Reveal Novel Features of Enhancers, Sex Chromosomes, piRNAs, Gametogenesis, and Inherited Small RNAs (Bisulfite-Seq) [Sperm]
     SRP400466     Multiplex Epigenome Editing of MECP2 to Rescue Rett Syndrome Neurons (WGBS) [ESC]
     SRP075292     Cumulative Impact of Polychlorinated Biphenyl and Large Chromosomal Duplications on DNA Methylation, Chromatin, and Expression of Autism Candidate Genes. [Brain, Neuroblastoma Cell Line, neuroblastoma cell line with extra copy of part of maternal chr15, neuroblastoma cell line with extra copy of part of maternal chr15 and part of chr22]
     SRP396513     Rockfish: Detection of 5mC DNA Modifications Using Raw Nanopore Signal [ESC, Purified Cardiomyocyte]
     SRP398111     to be updated [Blood]
     SRP336573     Perturbation of TET2 condensation induces genome-wide promiscuous DNA hypomethylation and curtails leukemia cell growth [ESCs (mESCs), Leukemia Cell Line]
     SRP397737     Global hypermethylation of intestinal epithelial cells is a hallmark feature of neonatal surgical necrotizing enterocolitis [lcm_colon_ileum] [Colon, Ileum]
     SRP397676     Loss of tight junctions disrupts gastrulation patterning and increases differentiation towards the germ cell lineage in human pluripotent stem cells [Skin Fibroblasts]
     SRP074852     DNMT and HDAC inhibitors globally induce cryptic TSSs encoded in long terminal repeats [NCI-H1299-EGFP/NEO]
     SRP396738     Highly efficient and rapid generation of human pluripotent stem cells by chemical reprogramming (WGBS) [Adult Human Adipose Derived Mesenchymal Stromal, Chemically Induced Pluripotent Stem Cell]
     SRP396408     Neonatal necrotizing enterocolitis-associated DNA methylation signatures in the colon are evident in stool samples of affected individuals [Colon, Stool]
     SRP396192     DNA Methylation Profile of Lip Tissue from Congenital Non-syndromic Cleft Lip and Palate Patients by Whole Genome Bisulfite Sequencing [Lip]
     SRP395427     WGBS-seq and oxWGBS-seq Atlas for Oral Squamous Cell Carcinoma [Normal Adjacent, OSCC]
     SRP012560     GSE34399: Replication Timing by Repli-seq from ENCODE/University of Washington [ESC, Skeletal Muscle Myoblast]
     SRP074177     Nucleation of DNA Repair Factors by FOXA1 Links DNA Demethylation to Transcriptional Pioneering [MCF-7 cells (siFOXA1-transfected), MCF-7 cells (siNS-transfected)]
     SRP394454     Methylation profile of latent metastatic (Lat-M) cells from clear cell renal cell carcinoma (ccRCC) [Kidney Cancer]
     SRP014634     Examination of four human tissue samples by MethylC-seq [Placenta From Full-Term Pregnancy]
     SRP049651     Large-scale epigenetic reprogramming is punctuated late during the evolution of pancreatic cancer progression [BS-Seq] [Liver Metastasis, Lung Metastasis, Normal Pancreas, Patient A38, Peritoneal Metastasis, Primary Tumor]
     SRP392105     Placental ischemia disrupts DNA methylation patterns of distal regulatory regions in rat [Placenta, Planceta]
     SRP389118     Comprehensive analyses of partially methylated domains and differentially methylated regions in esophageal cancer reveal both cell-type- and cancer-specific epigenetic regulation [WGBS] [Esophageal Adenocarcinoma, Esophageal Squamous Cell Carcinoma]
     SRP387971     Tonic-signaling chimeric antigen receptors drive human regulatory T cell exhaustion [CD4+ TCONV, CD4+ TREG]
     SRP072141     stem cell epigenomics [H1 stem cell]
     SRP072078     epigenomic analysis of lung and liver [Liver, Lung]
     SRP072075     Epigenomic analysis of lymphocytes and fibroblasts [Foreskin Fibroblasts, sorted CD4+ T cells]
     SRP072071     study of brain methylation [Brain Pre-Frontal Cortex]
     SRP071891     Functional Haploid Human Oocytes Generated from Polar Body Genomes (Bisulfite-Seq) [ESC, Polar Body Nuclear Transfer]
     SRP387319     Dysfunction of 5-methylcytosine oxidases and the Polycomb protein RYBP leads to widespread DNA hypermethylation and cell transformation [WGBS] [Bronchial]
     SRP387154     Accurate simultaneous sequencing of genetic and epigenetic bases in DNA [Blood]
     SRP071771     Identification of methylation haplotype blocks aids in deconvolution of heterogeneous tissue samples and tissue-of-origin mapping from plasma DNA [WGBS] [Liver, Skeletal Muscle]
     SRP386501     Multiplex Epigenome Editing of MECP2 to Rescue Rett Syndrome Neurons [ChIP-BS-Seq] [ESCs (hESC)]
     SRP304105     Large-scale manipulation of promoter DNA methylation reveals context-specific transcriptional responses and stability [Cell Line]
     SRP384348     Evidence that direct inhibition of transcription factor binding is the prevailing mode of gene and repeat repression by DNA methylation [WGBS-Seq] [Ebryonic Stem Cell, Embryonic Kidney, Ngn2 neurons]
     SRP013816     SINE transcription by RNA polymerase III is suppressed by histone methylation but not DNA methylation [HeLa cervical carcinoma]
     SRP377560     Reversible epigenetic alterations mediate PSMA expression heterogeneity in advanced metastatic prostate cancer. [Prostate Cancer Patient Derived Xenograft]
     SRP376918     Droplet-based bisulfite sequencing for high-throughput profiling of single-cell DNA methylomes [N.A.]
     SRP068579     Reversion to naïve human pluripotency creates a new methylation landscape devoid of blastocyst or germline memory [5iLAF SSEA4 negative UCLA1 EpiLC day 0, 5iLAF SSEA4 negative UCLA1 EpiLC day 16, 5iLAF SSEA4+ subpopulation UCLA1 hESCs, 5iLAF SSEA4-subpopulation UCLA1 hESCs, 5iLAF SSEA4-subpopulation UCLA20n hESCs, Primed SSEA4+ UCLA1 hESCs, Primed UCLA1 EpiLC day 0, Primed UCLA1 EpiLC day 16]
     SRP330251     Vitamin B12 regulates the transcriptomes of human ileal epithelial cells (iECs) [Ileum]
     SRP375137     DNMT3A-mediated DNA demethylation is required for hypoxia induced EMT of human cancer cells
     SRP373924     NOMe-Seq analysis of IMR-90 cell line II [IMR90]
     SRP373708     WGBS of primary and recurrent ovarian cancer tumors with and without BRCA1/2 mutations [Ovarian Cancer Tumors]
     SRP067779     Novel contribution of acetylated histone variant H2A.Z in activation of neo-enhancers in prostate cancer [NOMe-seq] [LNCaP clone FGC (ATCC CRL-1740). Androgen-sensitive human prostate adenocarcinoma, Primary prostate epithelial cells. Cambrex Bio Science Cat. No. CC-2555]
     SRP323101     RRBS-based quantitative methylation analysis define 100% methylation fidelity CpG sites [Blood, Retina]
     SRP368308     Lack of major genome-wide DNA methylation changes in succinate-treated human epithelial cells [Bronchial]
     SRP367891     DNA methylation analysis of malignant and normal uveal melanocytes reveals novel molecular features of uveal melanoma [Primary Culture, UM sorted]
     SRP085035     Molecular Criteria for Defining the Naive Human Pluripotent State [methylation profiling] [ESC, Naive human ESCs]
     SRP364929     human rDNA obesity [Blood]
     SRP012499     Epigenetic alterations of a DNMT3B-mutant ICF patient at base-pair resolution [Blood]
     SRP362494     The aberrant epigenome of DNMT3B-mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memory (WGBS) [iPSC]
     SRP000996     BI Human Reference Epigenome Mapping Project [CD184+ endoderm cultured, CD19, CD34 Primary Cells, Cell Line, Fetal Adrenal, Fetal Heart, Fetal Muscle Leg, Fetal Muscle Trunk, Fetal Placenta, Fetal Spinal Cord, Fetal Stomach, Fetal Thymus, IMR90, adult CD14, adult CD3, adult CD56]
     SRP358957     WGBS of OLD and YOUNG primary Fibroblasts [Arm Skin, Inguinal Area, NS, Umbilical Area]
     SRP353536     Transcriptome and Bisulfite sequencing of drug treated breast cancer cell lines [Mammary Gland]
     SRP012161     Evolutionary Significance of DNA Methylation in Human and Chimpanzee Brains [Prefrontal Cortex]
     SRP357372     WGBS and RNA-seq of HUVECs transfected with siNC or siTET2 [Umbilical Vein Endothelial Cells]
     SRP357363     Whole-genome bisulfite sequencing anaysis of PSCs [Feeder-free PSC]
     SRP356708     Young vs Old Fibroblast WGBS [Skin]
     SRP299802     Acute lymphoblastic leukemia displays a distinct highly methylated genome [Cell Line]
     SRP353982     methyl-Seq of Pediatric ARDS Nasal and Bronchial Brushings [Bronchial, Nasal]
     SRP353670     DNA Methylation Potential Energy Landscape Analysis of MLL-rearranged Acute Myeloid Leukemia (AML) and Normal hematopoietic precursors [WGBS] [Primary]
     SRP353340     NOMe-Seq analysis of IMR-90 cell line [IMR90]
     SRP353040     WGBS of control and DAC-treated tumor tissue from PDX model [Colorectal Cancer]
     SRP352189     CRISPR-based targeted haplotype-resolved assembly of a megabase region [WGBS] [B Cell]
     SRP348645     Transcriptomic and Epigenomic Profiles of CIC-knockout and IDH1 mutant cells [WGBS] [Immortalized Astrocyte Cells]
     SRP346999     Whole genome bilsufite sequencing of sgTET2 HepG2 [Missing]
     SRP346828     NOMe-HiC: joint profiling of genetic variants, DNA methylation, chromatin accessibility, and 3D genome in the same DNA molecule [Lung Fibroblast Cell Line]
     SRP011945     Base Resolution Analysis of 5-Hydroxymethylcytosine in the Mammalian Genome [ESC]
     SRP011746     Ultra-low-input, tagmentation-based whole genome bisulfite sequencing
     SRP345048     Antigen cross-presentation in young tumor-bearing hosts promotes CD8 T cell terminal differentiation [WGBS] [Germ Cell Tumor]
     SRP342964     scSPLAT, a scalable plate-based protocol for single cell WGBS library preparation [Blood]
     SRP339574     Methylation Mediated Silencing of Protein Kinase C Zeta Induces Apoptosis Avoidance through ATM/Chk-2 Inactivation in Dedifferentiated Chondrosarcoma [Chondrosarcoma Cell Line]
     SRP338853     DNA methylation of MOLM-13 cells [Cell Line]
     SRP338189     Deleting DNMT3A in CAR T cells prevents exhaustion and 1 enhances antitumor activity [T Cells]
     SRP337501     DNA methylation landscape and signature of CD4+ lymphocytes of lamina propria in Crohn's patients by reduced representation and bisulfite sequencing [BiSulfite-seq] [Isolated CD4+]
     SRP337159     Homo sapiens Epigenomics [Sperm]
     SRP337018     whole-genome wide DNA methylation aberration in HCC [Liver]
     SRP334550     Proinflammatory cytokines promote TET2-mediated DNA demethylation during CD8 T cell effector differentiation [CD8+ T Cells]
     SRP199025     Molecular mechanism of KCNJ5 gene hotspot mutation in adrenal aldosteronoma [Adrenal Gland]
     SRP332448     H3K9 dimethylation safeguards cancer cells against activation of the Interferon pathway [WGBS] [U937]
     SRP332277     Methyl-seq Human [Sperm]
     SRP332046     The WGBS and ATAC-seq from human serum and amniotic cell [Blood]
     SRP329794     Anchor-Based Bisulfite Sequencing determines genome-wide DNA methylation [Cell Line]
     SRP328700     Whole genome methylation profiliing between the IMU and KRT subtypes of HPV-associated head and neck cell carcinoma (HNSCC) [Head And Neck Cell Carcinoma]
     SRP268979     Loss of epigenetic suppression of retrotransposons with oncogenic potential in aging mammary luminal epithelial cells [Mammary Luminal Epithelial]
     SRP286872     Transient naive reprogramming corrects hiPS cells functionally and epigenetically [WGBS] [Blast, ESC, Keratinocytes, Mesenchymal Stem Cell, iPSC]
     SRP291325     Transient naive reprogramming corrects hiPS cells functionally and epigenetically [WGBS 2] [Cultured Human Fibroblasts, ESC, Pluripotent Stem Cell, Reprogramming Intermediate, iPSC]
     SRP325924     Distinct DNA methylation landscape between pediatric brain and adult brain [Cerebellum, Cerebrum]
     SRP325722     Chemical-based external stimulation reprograms human somatic cells into pluripotency (WGBS) [Adult Human Adipose Derived Mesenchymal Stromal, Chemically Induced Pluripotent Stem Cell, Embryonic Fibroblasts, hES cells H1, hES cells H9, somatic cells during chemical reprogramming stage I, somatic cells during chemical reprogramming stage II, somatic cells during chemical reprogramming stage II without 5azac, somatic cells during chemical reprogramming stage II without JNKIN8]
     SRP325428     Systematic profiling of DNMT3A variants reveals protein instability mediated by the DCAF8 E3 ubiquitin ligase adaptor [Cell Line, ESC]
     SRP321876     Genetic variation at mouse and human ribosomal DNA influences associated epigenetic states [Blood, Kidney]
     SRP325062     Cerebrospinal fluid cell-free DNA methylomes recapture pediatric medulloblastoma tissue's tumor feature [CSF, Tumor]
     SRP324100     Placental methylome reveals a 22q13.33 brain regulatory gene locus associated with autism [WGBS] [Placenta]
     SRP324016     Cerebrospinal fluid cell-free DNA methylomes subtyping pediatric medulloblastoma [Blast]
     SRP323990     Identification of DNA Methylation Predicts Onset of PTSD and Depression Following Trauma [PBMC]
     SRP323032     Mapping the glucocorticoid gene regulatory network and alterations that contribute to steroid resistance in childhood acute lymphoblastic leukemia [WGBS] [ALL]
     SRP321573     Conservation and divergence of DNA methylation patterns and functions in vertebrates [Primary Dermal Fibroblasts, Psoas Muscle]
     SRP320538     Dynamic patterns of DNA methylation in the normal prostate epithelial differentiation program are targets of aberrant methylation in prostate cancer [BiSulfite-seq] [Cell Line]
     SRP319892     Expanding highly homogenous population of human primordial germ cell like cells in long-term and feeder-free culture condition [WGBS] [EGC, freshly isolated human PGCLC, iPSC, long-term culture human PGCLC c56, long-term culture human PGCLC c63, long-term culture human PGCLC c71, long-term culture human PGCLC c84]
     SRP318399     DNA methylation profiles of four immune cell types from MS patients and healthy controls [Blood]
     SRP316873     Whole-Genome Bisulfite Sequencing of Nasopharyngeal Carcinoma and Nasopharyngeal Epithelial Tissues [SeqCapEpi] [Cell Line, Methylation Control]
     SRP059772     Whole genome analysis of the methylome and hydroxymethylome in normal and malignant lung and liver [oxBS-Seq and BS-Seq] [Liver, Lung]
     SRP316059     NSCLP-Twins [Saliva DNA]
     SRP315878     Homo sapiens Epigenomics [Blood, Bone Marrow]
     SRP315039     DNA methylome and genome sequencing of human ovarian epithelial cell line [Ovarian Epithelium]
     SRP314963     The proline and serine rich protein PROSER1 mediates O-GlcNAcylation of TET2 to regulate DNA demethylation on UTX-dependent enhancers and CpG islands [WGBS] [Embryonic Kidney]
     SRP059433     Gender Differences in Global but not Targeted Demethylation in iPSC Reprogramming [BS seq AIDKO MEF1, BS seq ESC 1, BS seq ESC 2, BS seq ESC 3, BS seq d6 Thy1 positive 1, BS seq d6 Thy1 positive 2, BS seq d6 Thy1 positive 3, Fibroblast, MEF, Reprogramming Fibroblast, iPSC]
     SRP059313     UPF : Methylation_primates [Blood]
     SRP059289     Conversion of Human Gastric Epithelial Cells to Multipotent Endodermal Progenitors using Defined Small Molecules [DNA methylation] [Stomach, hepatoctes induced by differentiation of hiMEPs, hiMEPs derived from GECs by reprogramming]
     SRP310254     DNMT3A haploinsufficiency causes dichotomous DNA methylation defects at enhancers in mature human immune cells [BiSulfite-seq] [hESC-derived macrophages]
     SRP268755     Probing the signaling requirements for naïve human pluripotency by high-throughput chemical screening [WGBS] [ESC, Nave hESC]
     SRP309472     Epigenetic crosstalk [KYSE-30]
     SRP309354     Stable DNMT3L Overexpression in SH-SY5Y Neurons Recreates a Facet of the Genome-Wide Down Syndrome DNA Methylation Signature [SH-SY5Y]
     SRP309314     Epigenomics of nasal mucosa in children with acute respiratory illness [Nasal Mucosa]
     SRP058102     Analysis of DNA Methylation in replication and cell cycle arrest. [Primary Dermal Fibroblasts]
     SRP050499     The Transcriptome and DNA Methylome Landscapes of Human Primordial Germ Cells [Brain, Gonadal Somatic Cells, Heart, Primordial Germ]
     SRP308854     Age-associated cryptic transcription in mammalian stem cells is linked to permissive chromatin at cryptic promoters [WGBS] [umbilical cord-derived mesenchymal stem cells (PCS-500-010 lot #63216949), umbilical cord-derived mesenchymal stem cells (PCS-500-010 lot #63216950)]
     SRP308810     Genome-wide Programmable Transcriptional Memory by CRISPR-based Epigenome Editing [HEK293T]
     SRP308490     Pan-cancer predictions of transcription factors mediating aberrant DNA methylation [HCC1954, hTERT-HME1]
     SRP304712     Epigenome profiling in gastric carcinogenesis by whole genome bisulfite sequencing [Normal, Stomach, Tumor]
     SRP304684     Inherent genomic properties underlie the epigenomic heterogeneity of human induced pluripotent stem cells [WGBS]
     SRP057450     A novel bivalent chromatin state exists at enhancers [HCT116]
     SRP008337     Role of DNMT3B in the regulation of early neural and neural crest specifiers [H9]
     SRP008144     Directional DNA methylation changes and complex intermediate states accompany lineage specificity in the adult hematopoietic compartment [B Cell, Cord Blood, HSPC, Neutrohphil]
     SRP007820     The DNA methylomes of a newborn and a centenarian [Blood, Cord Blood]
     SRP007400     Sperm methylation profiles reveal features of epigenetic inheritance and evolution in primates [Sperm]
     SRP006774     Increased methylation variation in epigenetic domains across cancer types
     SRP006728     Genome-wide DNA methylation mapping in breast cancer cells (HCC1954) and normal breast cells (HMEC) [Breast Cancer]
     SRP003529     Hotspots of aberrant epigenomic reprogramming in human induced pluripotent stem cells
     SRP001720     Dynamic Changes in the Human Methylome During Differentiation [ESC, Fibroblasts derived from human ESCs, Newborn Human Foreskin Fibroblasts]
     SRP000941     UCSD Human Reference Epigenome Mapping Project [Adipose, Adipose Tissue, Adrenal Gland, Aorta, Bladder, Cell Line, ESC, Esophagus, Gastric, IMR90, Left Ventricle, Liver, Lung, Ovary, Pancreas, Psoas Muscle, Right Atrium, Right Ventricle, Sigmoid Colon, Small Intestine, Spleen, Thymus]
     ERP139499     Whole genome bisulfite sequencing of liver samples of five mammals (human, rhesus macaque, mouse, rat and dog) [Liver]
     ERP135424     Single-cell methylation profiling of a twin pair discordant for common variable immunodeficiency [Memory B-Cell]
     ERP135121     Whole Genome Bisulfite Sequencing (WGBS) of the SH-SY5Y human neuroblastoma cell line [Bone Marrow]
     ERP009555     Effects of HIST1H2ac knockdown on the DNA methylation landscape of breast cancer cell line MCF-7 [MCF-7]
     ERP130693     Performance comparison and in-silico harmonisation of commercial platforms for DNA methylome analysis by targeted bisulfite sequencing
     ERP129475     DNA Methylation signature in mononuclear cells and proinflammatory cytokines in Meniere Disease [Blood]
     ERP109780     Whole-genome fingerprint of the DNA methylome during chemically induced differentiation of the AML cell line HL-60/S4 [HL60]
     ERP127251     Single Cell Multi-Omics of Human Preimplantation Embryos Demonstrates Susceptibility to Excess Glucocorticoid Exposure(BSseq part) [Whole Organism]
     ERP123063     Whole genome DNA methylation analysis of human embryonic stem cells
     ERP122802     Whole genome DNA methylation analysis of human testicular germ cells
     ERP122363     No evidence for intervention-associated DNA methylation changes in monocytes of patients with posttraumatic stress disorder or anorexia nervosa
     ERP005229     Whole-genome Bisulfite Sequencing for Methylation Analysis of human monocytes
     ERP117337     Whole genome DNA methylation analysis of sperm DNA from normozoospermic and oligoasthenoteratozoospermic men
     ERP004221     Genome-wide methylome profiling of normal breast and breast tumors [Breast, Breast Cancer]
     ERP114912     Genome-wide Analysis of the Nucleosome Landscape in Individuals with Coffin-Siris Syndrome
     ERP110315     Single molecule sequencing and assembly of flow sorted Y chromosome from HG02982 [Lymphoblastoid Cell Line]
     ERP110208     Whole genome methylation analysis of sperm and blood from young and old men. [Blood, Sperm]
     ERP106410     An integrated genomic analysis of L1 retrotransposon mosaicism in the brain [Hippocampus]
     ERP109664     Bisulphite-seq to investigate the proto CpG island methylator phenotype of sessile serrated adenoma/polyps, dataset 2 [Colon]
     ERP109610     Bisulphite-seq to investigate the proto CpG island methylator phenotype of sessile serrated adenoma/polyps [Colon]
     ERP107813     Bisulfite-seq of synovial biopsies from rheumatoid arthritis patients [Synovial Membrane]
     ERP010942     We present the first genome-scale analysis of the effect of CpG methylation on DNA-binding of TFs. [Embryo, GP5D, LHSAR cell with HOXB13 transduced, Lhsar, LoVo, VCap]
     ERP018009     Base resolution maps of mutations, 5-methylcytosine and 5-hydroxymethylcytosine, and transcriptome of blood, tumour and margin samples from a glioblastoma multiforme patient [Brain]
     ERP014223     DNA methylation profiling of human naive embryonic stem cells [Embryo]
     ERP011276     5Aza and TSA treatment of MCF7 cells (BS-seq) [Breast]
     ERP008742     Germ_cell_methylation_dynamics [308-D5 TE Embryo 1, 308-D5 TE Embryo 2, 693-D6 TE Embryo 2, A3 mPGCLC1, BS treated DNA PBAT library, C3 mPGCLC2, D2 mPGCLC1, D3 mPGCLC2, E3 mPGCLC2, ESC, F1 hPGCLC1, F2 mPGCLC1, F3 mPGCLC2, G2 mPGCLC1, G3 mPGCLC2, H3 mPGCLC2, P11(4), P14(2), P8(3), PRGp8 4, Passage 10 Sort 2, Passage 10 Sort 3, Passage 10 Sort 4, S6EOSKSR 1, S6EOSKSR 3, S6EOSp15 1, S6EOSp15 2, S6EOSp5 3, S6EOSp9 1, S6EOSp9 2, S6EOSp9 3, hES1, hES2, hES3, hEpiLC 2016214 2, hEpiLC 201635, hKSR2, hKSR3, mEpiLC E14 d1 1, mEpiLC E14 d2 2]
     ERP144942     Validation of differentially methylated DNA regions in colorectal precancerous lesions. [Colon]
     DRP012061     Epigenetic regulation by nitrosative stress as a potential mechanism of long COVID [Small Airway Epithelial]
     DRP014307     Transcriptomics and DNA methylome of human iPS cell lines [T-iPS, iPS]
     DRP008243     Transcriptome and methylome analyses of trophoblast stem-like cells derived from primed human embryonic stem cells [TSLprimed]
     DRP007001     Development of long-read whole genome methylation sequencing method using the enzymatic base conversion and the nanopore sequencing [BT-474, MDA-MB-231]
     DRP007963     Whole genome bisulfite sequencing of colorectal cancer [Metastatic Cancerous Tissue Obtained From Distant Lymph Node Metastasis, Metastatic Cancerous Tissue Obtained From Hepatic Metastasis, Metastatic Cancerous Tissue Obtained From Lung Metastasis, Primary Cancerous]
     DRP006124     DNA methylome analyses and expression analysis for malignant glioma harbouring H3F3A gene mutation [Glioma]
     DRP004736     Generation of human oogonia from induced pluripotent stem cells in vitro [PGCLC, aggregate cultured PGCLC, iMeLC, iPSC]
     DRP003407     Software updates in the Illumina HiSeq platform affect whole-genome bisulfite sequencing [EpiLC, IMR90, Spermatogonia]
     DRP001914     Omics catalogue of lung adenocarcinoma cell lines [Cell Line]
     Common     Common methbase tracks for the hg38 assembly
-   Mapping and Sequencing    
Base Position Chromosome position in bases. (Clicks here zoom in 3x)
Chromosome Band Chromosome Bands Localized by FISH Mapping Clones
Short Match Perfect Matches to Short Sequence ()
-   Genes and Gene Predictions    
NCBI RefSeq RefSeq genes from NCBI
-   Comparative Genomics    
Cactus 241-way Cactus Alignment & Conservation of Zoonomia Placental Mammals (241 Species)
Multiz 470-way Multiz Alignment & Conservation (470 mammals)