Contribution of septins to human platelet structure and function.
PMID:35832887
Characterizing collaborative transcription regulation with a graph-based deep learning approach.
PMID:35666736
Machine learning: its challenges and opportunities in plant system biology.
PMID:35575915
Potential role of KRAB-ZFP binding and transcriptional states on DNA methylation of retroelements in human male germ cells.
PMID:35315771
Prediction of transcription factors associated with DNA demethylation during human cellular development.
PMID:35142952
Histone acetylome-wide associations in immune cells from individuals with active Mycobacterium tuberculosis infection.
PMID:35102304
Cell-free DNA profiling informs all major complications of hematopoietic cell transplantation.
PMID:35058359
TIGER: The gene expression regulatory variation landscape of human pancreatic islets.
PMID:34644572
Integrative Epigenome Map of the Normal Human Prostate Provides Insights Into Prostate Cancer Predisposition.
PMID:34513844
Recommendations for the FAIRification of genomic track metadata.
PMID:34249331
Contribution of genetic and epigenetic changes to escape from X-chromosome inactivation.
PMID:34187555
Whole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development.
PMID:33797837
Molecular and computational approaches to map regulatory elements in 3D chromatin structure.
PMID:33741028
A plug and play microfluidic platform for standardized sensitive low-input chromatin immunoprecipitation.
PMID:33707229
Cross-species examination of X-chromosome inactivation highlights domains of escape from silencing.
PMID:33597016
Epigenetic signatures in cancer: proper controls, current challenges and the potential for clinical translation.
PMID:33568205
Deciphering the genetic code of DNA methylation.
PMID:33432324
UniPath: a uniform approach for pathway and gene-set based analysis of heterogeneity in single-cell epigenome and transcriptome profiles.
PMID:33275158
SVFX: a machine learning framework to quantify the pathogenicity of structural variants.
PMID:33168059
HMST-Seq-Analyzer: A new python tool for differential methylation and hydroxymethylation analysis in various DNA methylation sequencing data.
PMID:33163148
Ultrafast and scalable variant annotation and prioritization with big functional genomics data.
PMID:33060171
Ten simple rules for annotating sequencing experiments.
PMID:33017400
Computational methods and next-generation sequencing approaches to analyze epigenetics data: Profiling of methods and applications.
PMID:32941995
Multiomics data integration unveils core transcriptional regulatory networks governing cell-type identity.
PMID:32839455
Dysregulation of cancer genes by recurrent intergenic fusions.
PMID:32631391
Seq-ing answers: Current data integration approaches to uncover mechanisms of transcriptional regulation.
PMID:32612756
cfNOMe - A single assay for comprehensive epigenetic analyses of cell-free DNA.
PMID:32580754
Unravelling the complex genetics of common kidney diseases: from variants to mechanisms.
PMID:32514149
Complexities of Understanding Function from CKD-Associated DNA Variants.
PMID:32513823
Molecular networks in Network Medicine: Development and applications.
PMID:32307915
Completing the ENCODE3 compendium yields accurate imputations across a variety of assays and human biosamples.
PMID:32228713
epiCOLOC: Integrating Large-Scale and Context-Dependent Epigenomics Features for Comprehensive Colocalization Analysis.
PMID:32117461
The Promises and Challenges of Toxico-Epigenomics: Environmental Chemicals and Their Impacts on the Epigenome.
PMID:31950866
Mechanisms of tissue and cell-type specificity in heritable traits and diseases.
PMID:31913361
The ENCODE Portal as an Epigenomics Resource.
PMID:31751002
Reverse gene-environment interaction approach to identify variants influencing body-mass index in humans.
PMID:31538139
Druggable Transcriptional Networks in the Human Neurogenic Epigenome.
PMID:31530573
Tales from topographic oceans: topologically associated domains and cancer.
PMID:31505466
A cell-free DNA metagenomic sequencing assay that integrates the host injury response to infection.
PMID:31451660
WashU Epigenome Browser update 2019.
PMID:31165883
Making Sense of the Epigenome Using Data Integration Approaches.
PMID:30837884
Orientation-aware plasma cell-free DNA fragmentation analysis in open chromatin regions informs tissue of origin.
PMID:30808726
A genetic variant associated with multiple sclerosis inversely affects the expression of CD58 and microRNA-548ac from the same gene.
PMID:30730892
Machine Learning for Integrating Data in Biology and Medicine: Principles, Practice, and Opportunities.
PMID:30467459
From association to mechanism in complex disease genetics: the role of the 3D genome.
PMID:30268153
BRWD1 orchestrates epigenetic landscape of late B lymphopoiesis.
PMID:30250168
Candidate genes linking maternal nutrient exposure to offspring health via DNA methylation: a review of existing evidence in humans with specific focus on one-carbon metabolism.
PMID:30137462
The epiGenomic Efficient Correlator (epiGeEC) tool allows fast comparison of user datasets with thousands of public epigenomic datasets.
PMID:30052804
Entering the post-epigenomic age: back to epigenetics.
PMID:29593118
Enrichment analysis with EpiAnnotator.
PMID:29329372
Panomics for Precision Medicine.
PMID:29217119
Neuroimaging genomics in psychiatry-a translational approach.
PMID:29179742
The Encyclopedia of DNA elements (ENCODE): data portal update.
PMID:29126249
DBTSS/DBKERO for integrated analysis of transcriptional regulation.
PMID:29126224
Vitamin D Receptor Signaling and Cancer.
PMID:29080633
New insights into the epigenetics of inflammatory rheumatic diseases.
PMID:28905855
Translational Perspective on Epigenetics in Cardiovascular Disease.
PMID:28750703
Regions of common inter-individual DNA methylation differences in human monocytes: genetic basis and potential function.
PMID:28747224
Early Detection of Cancer in Blood Using Single-Cell Analysis: A Proposal.
PMID:28587830
Non-coding RNAs in cardiovascular diseases: diagnostic and therapeutic perspectives.
PMID:28430919
DeepBlueR: large-scale epigenomic analysis in R.
PMID:28334349
Conserved expression of transposon-derived non-coding transcripts in primate stem cells.
PMID:28245871
Clinical implications of genome-wide DNA methylation studies in acute myeloid leukemia.
PMID:28153026