Epigenetic alterations at distal enhancers are linked to proliferation in human breast cancer.
PMID:35350772
scREMOTE: Using multimodal single cell data to predict regulatory gene relationships and to build a computational cell reprogramming model.
PMID:35300460
TcoFBase: a comprehensive database for decoding the regulatory transcription co-factors in human and mouse.
PMID:34718747
Epigenetic Silencing of HER2 Expression during Epithelial-Mesenchymal Transition Leads to Trastuzumab Resistance in Breast Cancer.
PMID:34575017
Genetic variations of DNA bindings of FOXA1 and co-factors in breast cancer susceptibility.
PMID:34518541
Prioritization and functional analysis of GWAS risk loci for Barrett's esophagus and esophageal adenocarcinoma.
PMID:34505128
Pan-cancer analysis of non-coding recurrent mutations and their possible involvement in cancer pathogenesis.
PMID:34316701
Integrative Ranking of Enhancer Networks Facilitates the Discovery of Epigenetic Markers in Cancer.
PMID:34135941
Crosstalk between microRNA expression and DNA methylation drives the hormone-dependent phenotype of breast cancer.
PMID:33926515
EphA2 super-enhancer promotes tumor progression by recruiting FOSL2 and TCF7L2 to activate the target gene EphA2.
PMID:33712565
Ultrasound May Suppress Tumor Growth, Inhibit Inflammation, and Establish Tolerogenesis by Remodeling Innatome via Pathways of ROS, Immune Checkpoints, Cytokines, and Trained Immunity/Tolerance.
PMID:33628851
Iterative epigenomic analyses in the same single cell.
PMID:33627472
CONQUER: an interactive toolbox to understand functional consequences of GWAS hits.
PMID:33575630
Multi-omics analysis to identify susceptibility genes for colorectal cancer.
PMID:33481017
An integrative multi-omics network-based approach identifies key regulators for breast cancer.
PMID:33133424
Cancer and pH Dynamics: Transcriptional Regulation, Proteostasis, and the Need for New Molecular Tools.
PMID:32992762
Computational methods and next-generation sequencing approaches to analyze epigenetics data: Profiling of methods and applications.
PMID:32941995
regSNPs-ASB: A Computational Framework for Identifying Allele-Specific Transcription Factor Binding From ATAC-seq Data.
PMID:32850739
Identification and Analysis of p53-Regulated Enhancers in Hepatic Carcinoma.
PMID:32695760
Enhancer-Gene Interaction Analyses Identified the Epidermal Growth Factor Receptor as a Susceptibility Gene for Type 2 Diabetes Mellitus.
PMID:32602275
GREG-studying transcriptional regulation using integrative graph databases.
PMID:32055858
Whole-genome fingerprint of the DNA methylome during chemically induced differentiation of the human AML cell line HL-60/S4.
PMID:31988093
Cardioinformatics: the nexus of bioinformatics and precision cardiology.
PMID:31802103
CERENKOV3: Clustering and molecular network-derived features improve computational prediction of functional noncoding SNPs.
PMID:31797625
EnhancerAtlas 2.0: an updated resource with enhancer annotation in 586 tissue/cell types across nine species.
PMID:31740966
Comprehensive analysis of long noncoding RNA (lncRNA)-chromatin interactions reveals lncRNA functions dependent on binding diverse regulatory elements.
PMID:31484726
Identifying Putative Susceptibility Genes and Evaluating Their Associations with Somatic Mutations in Human Cancers.
PMID:31402092
Experimental Data-Mining Analyses Reveal New Roles of Low-Intensity Ultrasound in Differentiating Cell Death Regulatome in Cancer and Non-cancer Cells via Potential Modulation of Chromatin Long-Range Interactions.
PMID:31355136
Increased acetylation of H3K14 in the genomic regions that encode trained immunity enzymes in lysophosphatidylcholine-activated human aortic endothelial cells - Novel qualification markers for chronic disease risk factors and conditional DAMPs.
PMID:31153039
Linking aberrant chromatin features in chronic lymphocytic leukemia to transcription factor networks.
PMID:31118277
Increasing Upstream Chromatin Long-Range Interactions May Favor Induction of Circular RNAs in LysoPC-Activated Human Aortic Endothelial Cells.
PMID:31057422
Uncovering genetic mechanisms of kidney aging through transcriptomics, genomics, and epigenomics.
PMID:30784661
Runs of homozygosity associate with decreased risks of lung cancer in never-smoking East Asian females.
PMID:30410588
PINES: phenotype-informed tissue weighting improves prediction of pathogenic noncoding variants.
PMID:30359302
Nervous System Regionalization Entails Axial Allocation before Neural Differentiation.
PMID:30343898
De novo pattern discovery enables robust assessment of functional consequences of non-coding variants.
PMID:30256891
HACER: an atlas of human active enhancers to interpret regulatory variants.
PMID:30247654
Nascent RNA sequencing analysis provides insights into enhancer-mediated gene regulation.
PMID:30139328
Genome-Wide Analysis of Interchromosomal Interaction Probabilities Reveals Chained Translocations and Overrepresentation of Translocation Breakpoints in Genes in a Cutaneous T-Cell Lymphoma Cell Line.
PMID:29900125
MICMIC: identification of DNA methylation of distal regulatory regions with causal effects on tumorigenesis.
PMID:29871649
A Comprehensive cis-eQTL Analysis Revealed Target Genes in Breast Cancer Susceptibility Loci Identified in Genome-wide Association Studies.
PMID:29727689
An Osteoporosis Risk SNP at 1p36.12 Acts as an Allele-Specific Enhancer to Modulate LINC00339 Expression via Long-Range Loop Formation.
PMID:29706346
Enhancing the Promise of Drug Repositioning through Genetics.
PMID:29270124
EpiDenovo: a platform for linking regulatory de novo mutations to developmental epigenetics and diseases.
PMID:29040751
Loci associated with skin pigmentation identified in African populations.
PMID:29025994
Identifying DNase I hypersensitive sites as driver distal regulatory elements in breast cancer.
PMID:28874753
VEXOR: an integrative environment for prioritization of functional variants in fine-mapping analysis.
PMID:28453673
Network Reconstruction Reveals that Valproic Acid Activates Neurogenic Transcriptional Programs in Adult Brain Following Traumatic Injury.
PMID:28271248
Software tools for visualizing Hi-C data.
PMID:28159004
Statistical challenges in analyzing methylation and long-range chromosomal interaction data.
PMID:28008337
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.
PMID:27796716
Comparative Methylome Analyses Identify Epigenetic Regulatory Loci of Human Brain Evolution.
PMID:27563052
LOGIQA: a database dedicated to long-range genome interactions quality assessment.
PMID:27185059
3CDB: a manually curated database of chromosome conformation capture data.
PMID:27081154
Enhancer methylation dynamics contribute to cancer plasticity and patient mortality.
PMID:26907635
Progress and challenges in bioinformatics approaches for enhancer identification.
PMID:26634919
In the loop: promoter-enhancer interactions and bioinformatics.
PMID:26586731
LncRNA ontology: inferring lncRNA functions based on chromatin states and expression patterns.
PMID:26485761
DENdb: database of integrated human enhancers.
PMID:26342387