Functional Genomics Analysis to Disentangle the Role of Genetic Variants in Major Depression.
PMID:35886042
Discovering the drivers of clonal hematopoiesis.
PMID:35871184
DESSO-DB: A web database for sequence and shape motif analyses and identification.
PMID:35782725
The hypoxia-induced changes in miRNA-mRNA in RNA-induced silencing complexes and HIF-2 induced miRNAs in human endothelial cells.
PMID:35713587
Ranking reprogramming factors for cell differentiation.
PMID:35710610
Virtual ChIP-seq: predicting transcription factor binding by learning from the transcriptome.
PMID:35681170
ARID1B, a molecular suppressor of erythropoiesis, is essential for the prevention of Monge's disease.
PMID:35672450
Integrating 3D genomic and epigenomic data to enhance target gene discovery and drug repurposing in transcriptome-wide association studies.
PMID:35672318
EHF is a novel regulator of cellular redox metabolism and predicts patient prognosis in HNSCC.
PMID:35664541
FABIAN-variant: predicting the effects of DNA variants on transcription factor binding.
PMID:35639768
Prediction of protein-ligand binding affinity from sequencing data with interpretable machine learning.
PMID:35606422
3DCoop: An approach for computational inference of cell-type-specific transcriptional regulators cooperation in 3D chromatin.
PMID:35600920
Compatibility rules of human enhancer and promoter sequences.
PMID:35594906
Genome-wide analysis of cis-regulatory changes underlying metabolic adaptation of cavefish.
PMID:35551306
Reorganization of postmitotic neuronal chromatin accessibility for maturation of serotonergic identity.
PMID:35471146
A leukemia-protective germline variant mediates chromatin module formation via transcription factor nucleation.
PMID:35440565
Cooperative interaction between ERα and the EMT-inducer ZEB1 reprograms breast cancer cells for bone metastasis.
PMID:35440541
Machine Learning Prediction of Non-Coding Variant Impact in Human Retinal cis-Regulatory Elements.
PMID:35435921
Multi-omics protein-coding units as massively parallel Bayesian networks: Empirical validation of causality structure.
PMID:35355520
Nuclear receptor activation shapes spatial genome organization essential for gene expression control: lessons learned from the vitamin D receptor.
PMID:35325193
Deciphering the Retinal Epigenome during Development, Disease and Reprogramming: Advancements, Challenges and Perspectives.
PMID:35269428
Base-resolution prediction of transcription factor binding signals by a deep learning framework.
PMID:35263332
KLF15 cistromes reveal a hepatocyte pathway governing plasma corticosteroid transport and systemic inflammation.
PMID:35263131
Coordinated Cross-Talk Between the Myc and Mlx Networks in Liver Regeneration and Neoplasia.
PMID:35259493
CASCADE: high-throughput characterization of regulatory complex binding altered by non-coding variants.
PMID:35252945
Bone Marrow Stroma-Induced Transcriptome and Regulome Signatures of Multiple Myeloma.
PMID:35205675
EZH2 Mediates Proliferation, Migration, and Invasion Promoted by Estradiol in Human Glioblastoma Cells.
PMID:35197928
Tcf1 preprograms the mobilization of glycolysis in central memory CD8+ T cells during recall responses.
PMID:35190717
Uncovering the mesendoderm gene regulatory network through multi-omic data integration.
PMID:35172134
Biallelic mutations in cancer genomes reveal local mutational determinants.
PMID:35145300
Aberrant somatic hypermutation of CCND1 generates non-coding drivers of mantle cell lymphomagenesis.
PMID:35145272
Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease.
PMID:35132965
TNF-α-producing macrophages determine subtype identity and prognosis via AP1 enhancer reprogramming in pancreatic cancer.
PMID:35122059
MYC overexpression leads to increased chromatin interactions at super-enhancers and MYC binding sites.
PMID:35115371
CT-FOCS: a novel method for inferring cell type-specific enhancer-promoter maps.
PMID:35100425
spatzie: an R package for identifying significant transcription factor motif co-enrichment from enhancer-promoter interactions.
PMID:35100401
Transcription factor regulation of eQTL activity across individuals and tissues.
PMID:35100260
Identifying differential regulatory control of APOE ɛ4 on African versus European haplotypes as potential therapeutic targets.
PMID:34978147
Statistical estimates of multiple transcription factors binding in the model plant genomes based on ChIP-seq data.
PMID:34953471
Chromatin accessibility and microRNA expression in nephron progenitor cells during kidney development.
PMID:34942352
A comprehensive transcription factor and DNA-binding motif resource for the construction of gene regulatory networks in Botrytis cinerea and Trichoderma atroviride.
PMID:34900134
Interrogating cell type-specific cooperation of transcriptional regulators in 3D chromatin.
PMID:34888502
Cell-type specialization is encoded by specific chromatin topologies.
PMID:34789882
Explainable deep neural networks for novel viral genome prediction.
PMID:34764607
Factorbook: an updated catalog of transcription factor motifs and candidate regulatory motif sites.
PMID:34755879
ImmReg: the regulon atlas of immune-related pathways across cancer types.
PMID:34755873
Comparative Analyses of Sperm DNA Methylomes Among Three Commercial Pig Breeds Reveal Vital Hypomethylated Regions Associated With Spermatogenesis and Embryonic Development.
PMID:34691153
Global Histone H3 Lysine 4 Trimethylation (H3K4me3) Landscape Changes in Response to TGFβ.
PMID:34671716
TET2 mutations are associated with hypermethylation at key regulatory enhancers in normal and malignant hematopoiesis.
PMID:34663818
Detection of Neanderthal Adaptively Introgressed Genetic Variants That Modulate Reporter Gene Expression in Human Immune Cells.
PMID:34662402
The dynamic, combinatorial cis-regulatory lexicon of epidermal differentiation.
PMID:34650237
A global screening identifies chromatin-enriched RNA-binding proteins and the transcriptional regulatory activity of QKI5 during monocytic differentiation.
PMID:34649616
Chromatin Velocity reveals epigenetic dynamics by single-cell profiling of heterochromatin and euchromatin.
PMID:34635836
Bevacizumab-induced hypertension and proteinuria: a genome-wide study of more than 1000 patients.
PMID:34616010
Assessing deep learning methods in cis-regulatory motif finding based on genomic sequencing data.
PMID:34607350
SBSA: an online service for somatic binding sequence annotation.
PMID:34606615
Systematic Evaluation of DNA Sequence Variations on in vivo Transcription Factor Binding Affinity.
PMID:34567058
Tumor Necrosis Factor-alpha utilizes MAPK/NFκB pathways to induce cholesterol-25 hydroxylase for amplifying pro-inflammatory response via 25-hydroxycholesterol-integrin-FAK pathway.
PMID:34551004
The transcription factor reservoir and chromatin landscape in activated plasmacytoid dendritic cells.
PMID:34544361
Parallel characterization of cis-regulatory elements for multiple genes using CRISPRpath.
PMID:34524848
Chromatin-based, in cis and in trans regulatory rewiring underpins distinct oncogenic transcriptomes in multiple myeloma.
PMID:34521827
Information content differentiates enhancers from silencers in mouse photoreceptors.
PMID:34486522
YAP and TAZ are transcriptional co-activators of AP-1 proteins and STAT3 during breast cellular transformation.
PMID:34463254
Autosomal sex-associated co-methylated regions predict biological sex from DNA methylation.
PMID:34403484
Filtering of Data-Driven Gene Regulatory Networks Using Drosophila melanogaster as a Case Study.
PMID:34394179
Altered regulation of DPF3, a member of the SWI/SNF complexes, underlies the 14q24 renal cancer susceptibility locus.
PMID:34390653
Discovering differential genome sequence activity with interpretable and efficient deep learning.
PMID:34370721
Loss of the MAF Transcription Factor in Laryngeal Squamous Cell Carcinoma.
PMID:34356658
Direct characterization of cis-regulatory elements and functional dissection of complex genetic associations using HCR-FlowFISH.
PMID:34326544
A Panel of rSNPs Demonstrating Allelic Asymmetry in Both ChIP-seq and RNA-seq Data and the Search for Their Phenotypic Outcomes through Analysis of DEGs.
PMID:34298860
Meiotic recombination mirrors patterns of germline replication in mice and humans.
PMID:34260899
EGR1 and RXRA transcription factors link TGF-β pathway and CCL2 expression in triple negative breast cancer cells.
PMID:34239022
Differential gene expression identifies a transcriptional regulatory network involving ER-alpha and PITX1 in invasive epithelial ovarian cancer.
PMID:34215221
Regulatory SNPs: Altered Transcription Factor Binding Sites Implicated in Complex Traits and Diseases.
PMID:34208629
Profiling DNA break sites and transcriptional changes in response to contextual fear learning.
PMID:34197463
A Bayesian inference transcription factor activity model for the analysis of single-cell transcriptomes.
PMID:34193535
Accurate prediction of cis-regulatory modules reveals a prevalent regulatory genome of humans.
PMID:34159315
Genomic imprinting in mouse blastocysts is predominantly associated with H3K27me3.
PMID:34155196
Mapping chromatin accessibility and active regulatory elements reveals pathological mechanisms in human gliomas.
PMID:34131149
Skin and gut imprinted helper T cell subsets exhibit distinct functional phenotypes in central nervous system autoimmunity.
PMID:34099917
Plasma Membrane Calcium ATPase Regulates Stoichiometry of CD4+ T-Cell Compartments.
PMID:34093590
Transcription factor enrichment analysis (TFEA) quantifies the activity of multiple transcription factors from a single experiment.
PMID:34079046
Widespread Exaptation of L1 Transposons for Transcription Factor Binding in Breast Cancer.
PMID:34070697
A cross-cohort analysis of autosomal DNA methylation sex differences in the term placenta.
PMID:34044884
Transcription Factor-Binding Site Identification and Enrichment Analysis.
PMID:34033108
Use of scREAD to explore and analyze single-cell and single-nucleus RNA-seq data for Alzheimer's disease.
PMID:34013209
Diverse Molecular Mechanisms Contribute to Differential Expression of Human Duplicated Genes.
PMID:34009325
Integrative methylome-transcriptome analysis unravels cancer cell vulnerabilities in infant MLL-rearranged B cell acute lymphoblastic leukemia.
PMID:33983906
Landscape of allele-specific transcription factor binding in the human genome.
PMID:33980847
Genome-wide histone acetylation analysis reveals altered transcriptional regulation in the Parkinson's disease brain.
PMID:33947435
Bayesian Markov models improve the prediction of binding motifs beyond first order.
PMID:33928244
Statistical mechanics meets single-cell biology.
PMID:33875884
Deep neural networks identify sequence context features predictive of transcription factor binding.
PMID:33796819
Epigenomic tensor predicts disease subtypes and reveals constrained tumor evolution.
PMID:33789109
Auto-aggressive CXCR6+ CD8 T cells cause liver immune pathology in NASH.
PMID:33762736
A hierarchical regulatory network analysis of the vitamin D induced transcriptome reveals novel regulators and complete VDR dependency in monocytes.
PMID:33753848
Fast decoding cell type-specific transcription factor binding landscape at single-nucleotide resolution.
PMID:33741685
Single Cell RNA-Seq and Machine Learning Reveal Novel Subpopulations in Low-Grade Inflammatory Monocytes With Unique Regulatory Circuits.
PMID:33708217
Transcriptional Profiling of STAT1 Gain-of-Function Reveals Common and Mutation-Specific Fingerprints.
PMID:33679782
The glucocorticoid receptor recruits the COMPASS complex to regulate inflammatory transcription at macrophage enhancers.
PMID:33567280
Regulatory genomic circuitry of human disease loci by integrative epigenomics.
PMID:33536621
Locating transcription factor binding sites by fully convolutional neural network.
PMID:33498086
Cell lineage-specific methylome and genome alterations in gout.
PMID:33493135
Mitochondrial TSPO Deficiency Triggers Retrograde Signaling in MA-10 Mouse Tumor Leydig Cells.
PMID:33383772
Integrative Single-Cell RNA-Seq and ATAC-Seq Analysis of Human Developmental Hematopoiesis.
PMID:33352111
Genes associated with cognitive performance in the Morris water maze: an RNA-seq study.
PMID:33328525
The MUC5B-associated variant rs35705950 resides within an enhancer subject to lineage- and disease-dependent epigenetic remodeling.
PMID:33320836
Evidence of widespread, independent sequence signature for transcription factor cobinding.
PMID:33303494
Single-cell lineage analysis reveals extensive multimodal transcriptional control during directed beta-cell differentiation.
PMID:33257854
A map of cis-regulatory elements and 3D genome structures in zebrafish.
PMID:33239788
GTRD: an integrated view of transcription regulation.
PMID:33231677
Dedifferentiation and neuronal repression define familial Alzheimer's disease.
PMID:33188013
Exploring functionally annotated transcriptional consensus regulatory elements with CONREL.
PMID:33186463
Learning and interpreting the gene regulatory grammar in a deep learning framework.
PMID:33137083
Meta-Analysis of Transcriptome Data Detected New Potential Players in Response to Dioxin Exposure in Humans.
PMID:33113971
VARAdb: a comprehensive variation annotation database for human.
PMID:33095866
Analyzing a putative enhancer of optic disc morphology.
PMID:33092545
Disruptive natural selection by male reproductive potential prevents underexpression of protein-coding genes on the human Y chromosome as a self-domestication syndrome.
PMID:33092533
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells.
PMID:33057200
HIV-1 infection activates endogenous retroviral promoters regulating antiviral gene expression.
PMID:33021676
Long Noncoding RNA OIP5-AS1 Promotes Cell Apoptosis and Cataract Formation by Blocking POLG Expression Under Oxidative Stress.
PMID:33006594
TENET 2.0: Identification of key transcriptional regulators and enhancers in lung adenocarcinoma.
PMID:32925947
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
PMID:32888494
Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.
PMID:32879140
hTFtarget: A Comprehensive Database for Regulations of Human Transcription Factors and Their Targets.
PMID:32858223
ATAC-seq footprinting unravels kinetics of transcription factor binding during zygotic genome activation.
PMID:32848148
Asymmetric Conservation within Pairs of Co-Occurred Motifs Mediates Weak Direct Binding of Transcription Factors in ChIP-Seq Data.
PMID:32825662
Motto: Representing Motifs in Consensus Sequences with Minimum Information Loss.
PMID:32816922
Transcriptomic and epigenomic dynamics associated with development of human iPSC-derived GABAergic interneurons.
PMID:32794569
Metabolic effects of air pollution exposure and reversibility.
PMID:32780721
Integrative analyses of single-cell transcriptome and regulome using MAESTRO.
PMID:32767996
ABC-GWAS: Functional Annotation of Estrogen Receptor-Positive Breast Cancer Genetic Variants.
PMID:32765587
Memory Sequencing Reveals Heritable Single-Cell Gene Expression Programs Associated with Distinct Cellular Behaviors.
PMID:32735851
Global reference mapping of human transcription factor footprints.
PMID:32728250
DNA methylation enables transposable element-driven genome expansion.
PMID:32719115
The Meningioma Enhancer Landscape Delineates Novel Subgroups and Drives Druggable Dependencies.
PMID:32703768
MAGGIE: leveraging genetic variation to identify DNA sequence motifs mediating transcription factor binding and function.
PMID:32657363
Systemic Investigation of Promoter-wide Methylome and Genome Variations in Gout.
PMID:32630231
Seq-ing answers: Current data integration approaches to uncover mechanisms of transcriptional regulation.
PMID:32612756
Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma.
PMID:32483191
A parallelized, automated platform enabling individual or sequential ChIP of histone marks and transcription factors.
PMID:32461370
IRIS3: integrated cell-type-specific regulon inference server from single-cell RNA-Seq.
PMID:32421805
KAP1 Is a Chromatin Reader that Couples Steps of RNA Polymerase II Transcription to Sustain Oncogenic Programs.
PMID:32402252
Insights gained from a comprehensive all-against-all transcription factor binding motif benchmarking study.
PMID:32393327
Controlling gene activation by enhancers through a drug-inducible topological insulator.
PMID:32369019
Epigenetic regulation of neuronal cell specification inferred with single cell "Omics" data.
PMID:32368329
Deactivation of Glutaminolysis Sensitizes PIK3CA-Mutated Colorectal Cancer Cells to Aspirin-Induced Growth Inhibition.
PMID:32365457
Single-nucleus RNA-seq identifies divergent populations of FSHD2 myotube nuclei.
PMID:32365093
TFmotifView: a webserver for the visualization of transcription factor motifs in genomic regions.
PMID:32324215
Leveraging mouse chromatin data for heritability enrichment informs common disease architecture and reveals cortical layer contributions to schizophrenia.
PMID:32303558
Sporadic activation of an oxidative stress-dependent NRF2-p53 signaling network in breast epithelial spheroids and premalignancies.
PMID:32291314
Remodeling of active endothelial enhancers is associated with aberrant gene-regulatory networks in pulmonary arterial hypertension.
PMID:32245974
The physical basis and practical consequences of biological promiscuity.
PMID:32244231
Krüppel-like factor 3 (KLF3) suppresses NF-κB-driven inflammation in mice.
PMID:32213596
Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria.
PMID:32208162
DNA methylation disruption reshapes the hematopoietic differentiation landscape.
PMID:32203468
LogoJS: a Javascript package for creating sequence logos and embedding them in web applications.
PMID:32181813
HNF1A recruits KDM6A to activate differentiated acinar cell programs that suppress pancreatic cancer.
PMID:32154941
Epigenetic modulation of AREL1 and increased HLA expression in brains of multiple system atrophy patients.
PMID:32151281
Glycosylation of immunoglobulin G is regulated by a large network of genes pleiotropic with inflammatory diseases.
PMID:32128391
Differential Allele-Specific Expression Uncovers Breast Cancer Genes Dysregulated by Cis Noncoding Mutations.
PMID:32078798
Candidate SNP Markers of Atherogenesis Significantly Shifting the Affinity of TATA-Binding Protein for Human Gene Promoters show stabilizing Natural Selection as a Sum of Neutral Drift Accelerating Atherogenesis and Directional Natural Selection Slowing It.
PMID:32033288
Towards a comprehensive catalogue of validated and target-linked human enhancers.
PMID:31988385
A curated benchmark of enhancer-gene interactions for evaluating enhancer-target gene prediction methods.
PMID:31969180
A Novel Approach to Identify Enhancer lincRNAs by Integrating Genome, Epigenome, and Regulatome.
PMID:31956652
Rad51 paralogs and the risk of unselected breast cancer: A case-control study.
PMID:31905201
Combinatorial interactions of the LEC1 transcription factor specify diverse developmental programs during soybean seed development.
PMID:31892538
Lessons from eRNAs: understanding transcriptional regulation through the lens of nascent RNAs.
PMID:31856658
Early chromatin shaping predetermines multipotent vagal neural crest into neural, neuronal and mesenchymal lineages.
PMID:31792380
Sharing DNA-binding information across structurally similar proteins enables accurate specificity determination.
PMID:31777934
TFregulomeR reveals transcription factors' context-specific features and functions.
PMID:31754708
A single ChIP-seq dataset is sufficient for comprehensive analysis of motifs co-occurrence with MCOT package.
PMID:31750523
Improved linking of motifs to their TFs using domain information.
PMID:31742324
What Do Neighbors Tell About You: The Local Context of Cis-Regulatory Modules Complicates Prediction of Regulatory Variants.
PMID:31737053
JASPAR 2020: update of the open-access database of transcription factor binding profiles.
PMID:31701148
NPInter v4.0: an integrated database of ncRNA interactions.
PMID:31670377
Retrotransposons spread potential cis-regulatory elements during mammary gland evolution.
PMID:31642473
Reconstruction of the Global Neural Crest Gene Regulatory Network In Vivo.
PMID:31639368
Spliceosomal disruption of the non-canonical BAF complex in cancer.
PMID:31597964
MS-Based Approaches Enable the Structural Characterization of Transcription Factor/DNA Response Element Complex.
PMID:31561554
Pathway Analysis Integrating Genome-Wide and Functional Data Identifies PLCG2 as a Candidate Gene for Age-Related Macular Degeneration.
PMID:31560769
CGGBP1 regulates CTCF occupancy at repeats.
PMID:31547883
A Multi-Layered Study on Harmonic Oscillations in Mammalian Genomics and Proteomics.
PMID:31533246
Deep insights into the response of human cervical carcinoma cells to a new cyano enone-bearing triterpenoid soloxolone methyl: a transcriptome analysis.
PMID:31523389
Nascent transcript analysis of glucocorticoid crosstalk with TNF defines primary and cooperative inflammatory repression.
PMID:31519741
Reconstruction and Analysis of Gene Networks of Human Neurotransmitter Systems Reveal Genes with Contentious Manifestation for Anxiety, Depression, and Intellectual Disabilities.
PMID:31514272
Deciphering epigenomic code for cell differentiation using deep learning.
PMID:31510916
SalMotifDB: a tool for analyzing putative transcription factor binding sites in salmonid genomes.
PMID:31477007
A bioinformatic analysis identifies circadian expression of splicing factors and time-dependent alternative splicing events in the HD-MY-Z cell line.
PMID:31363108
Roles of p53 Family Structure and Function in Non-Canonical Response Element Binding and Activation.
PMID:31357595
Epigenomics and Single-Cell Sequencing Define a Developmental Hierarchy in Langerhans Cell Histiocytosis.
PMID:31345789
Benchmark and integration of resources for the estimation of human transcription factor activities.
PMID:31340985
Identification of DNA motifs that regulate DNA methylation.
PMID:31334813
Single Nucleotide Polymorphisms at a Distance from Aryl Hydrocarbon Receptor (AHR) Binding Sites Influence AHR Ligand-Dependent Gene Expression.
PMID:31292129
Computer genomics research at the bioinformatics conference series in Novosibirsk.
PMID:31291908
Low-Affinity Binding Sites and the Transcription Factor Specificity Paradox in Eukaryotes.
PMID:31283382
Unified single-cell analysis of testis gene regulation and pathology in five mouse strains.
PMID:31237565
Genome-wide enhancer annotations differ significantly in genomic distribution, evolution, and function.
PMID:31221079
Genetic resistance to DEHP-induced transgenerational endocrine disruption.
PMID:31181066
Comprehensive study of nuclear receptor DNA binding provides a revised framework for understanding receptor specificity.
PMID:31175293
ChEA3: transcription factor enrichment analysis by orthogonal omics integration.
PMID:31114921
QBiC-Pred: quantitative predictions of transcription factor binding changes due to sequence variants.
PMID:31114870
Integration of multiple epigenomic marks improves prediction of variant impact in saturation mutagenesis reporter assay.
PMID:31106481
TAGOOS: genome-wide supervised learning of non-coding loci associated to complex phenotypes.
PMID:31045203
ZFP30 promotes adipogenesis through the KAP1-mediated activation of a retrotransposon-derived Pparg2 enhancer.
PMID:31000713
Epigenetic-genetic chromatin footprinting identifies novel and subject-specific genes active in prefrontal cortex neurons.
PMID:30970224
cisTopic: cis-regulatory topic modeling on single-cell ATAC-seq data.
PMID:30962623
Primary endothelial cell-specific regulation of hypoxia-inducible factor (HIF)-1 and HIF-2 and their target gene expression profiles during hypoxia.
PMID:30917010
Computational analysis of the evolutionarily conserved Missing In Metastasis/Metastasis Suppressor 1 gene predicts novel interactions, regulatory regions and transcriptional control.
PMID:30858428
Epigenetic regulation of REX1 expression and chromatin binding specificity by HMGNs.
PMID:30838422
Sequence Characteristics Distinguish Transcribed Enhancers from Promoters and Predict Their Breadth of Activity.
PMID:30696717
Tissue-Specific Trans Regulation of the Mouse Epigenome.
PMID:30593494
Heterodimeric DNA motif synthesis and validations.
PMID:30590725
The Identification and Interpretation of cis-Regulatory Noncoding Mutations in Cancer.
PMID:30577431
Anchor: trans-cell type prediction of transcription factor binding sites.
PMID:30567711
GTRD: a database on gene transcription regulation-2019 update.
PMID:30445619
Functional regulatory mechanism of smooth muscle cell-restricted LMOD1 coronary artery disease locus.
PMID:30444878
MethMotif: an integrative cell specific database of transcription factor binding motifs coupled with DNA methylation profiles.
PMID:30380113
ELMER v.2: an R/Bioconductor package to reconstruct gene regulatory networks from DNA methylation and transcriptome profiles.
PMID:30364927
Genome-wide map of human and mouse transcription factor binding sites aggregated from ChIP-Seq data.
PMID:30352610
Control of directionality of chromatin folding for the inter- and intra-domain contacts at the Tfap2c-Bmp7 locus.
PMID:30213272
AnimalTFDB 3.0: a comprehensive resource for annotation and prediction of animal transcription factors.
PMID:30204897
Detecting genome-wide directional effects of transcription factor binding on polygenic disease risk.
PMID:30177862
A network of epigenomic and transcriptional cooperation encompassing an epigenomic master regulator in cancer.
PMID:29977600
c-Myc is a novel Leishmania virulence factor by proxy that targets the host miRNA system and is essential for survival in human macrophages.
PMID:29934305
The BaMM web server for de-novo motif discovery and regulatory sequence analysis.
PMID:29846656
Molecular and Functional Sex Differences of Noradrenergic Neurons in the Mouse Locus Coeruleus.
PMID:29791834
Differential Expression Profiling of Long Noncoding RNA and mRNA during Osteoblast Differentiation in Mouse.
PMID:29765976
Detecting Differential Transcription Factor Activity from ATAC-Seq Data.
PMID:29748466
PWMScan: a fast tool for scanning entire genomes with a position-specific weight matrix.
PMID:29514181
Assessing sufficiency and necessity of enhancer activities for gene expression and the mechanisms of transcription activation.
PMID:29491135