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. 
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                                    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