GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications. - Wikidata - awgldk - TriplyDB

GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications.

GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications.

http://www.wikidata.org/entity/Q36954041

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Making sense of GWAS: using epigenomics and genome engineering to understand the functional relevance of SNPs in non-coding regions of the human genome Epigenetic Research of Neurodegenerative Disorders Using Patient iPSC-Based Models Connecting SNPs in Diabetes: A Spatial Analysis of Meta-GWAS Loci High-density genotyping of immune-related loci identifies new SLE risk variants in individuals with Asian ancestry ORegAnno 3.0: a community-driven resource for curated regulatory annotation GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database dbPSHP: a database of recent positive selection across human populations.Interrogation of allelic chromatin states in human cells by high-density ChIP-genotyping.Associating disease-related genetic variants in intergenic regions to the genes they impact Role of non-coding sequence variants in cancer.Enlight: web-based integration of GWAS results with biological annotations Inference of gene-phenotype associations via protein-protein interaction and orthology.Computational Characterization of Osteoporosis Associated SNPs and Genes Identified by Genome-Wide Association Studies QuIN: A Web Server for Querying and Visualizing Chromatin Interaction Networks Pathway analysis supports association of nonsyndromic cryptorchidism with genetic loci linked to cytoskeleton-dependent functions.A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes rVarBase: an updated database for regulatory features of human variants.GWASdb v2: an update database for human genetic variants identified by genome-wide association studies.3D genome organization in health and disease: emerging opportunities in cancer translational medicine.A childhood acute lymphoblastic leukemia genome-wide association study identifies novel sex-specific risk variants.Evaluating the impact of single nucleotide variants on transcription factor binding.In the loop: promoter-enhancer interactions and bioinformatics.3DSNP: a database for linking human noncoding SNPs to their three-dimensional interacting genes.The missing story behind Genome Wide Association Studies: single nucleotide polymorphisms in gene deserts have a story to tell.Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci.cepip: context-dependent epigenomic weighting for prioritization of regulatory variants and disease-associated genes.Computational analyses of type 2 diabetes-associated loci identified by genome-wide association studies.The Role of Noncoding Genetic Variation in Isolated Orofacial Clefts.Rising Strengths Hong Kong SAR in Bioinformatics.Mining the Unknown: Assigning Function to Noncoding Single Nucleotide Polymorphisms.GSuite HyperBrowser: integrative analysis of dataset collections across the genome and epigenome RAPIDSNPs: A new computational pipeline for rapidly identifying key genetic variants reveals previously unidentified SNPs that are significantly associated with individual platelet responses Genomewide Association Study of Alcohol Dependence Identifies Risk Loci Altering Ethanol-Response Behaviors in Model Organisms.Molecular mechanisms underlying noncoding risk variations in psychiatric genetic studies Functional variomics and network perturbation: connecting genotype to phenotype in cancer.Intergenic GWAS SNPs are key components of the spatial and regulatory network for human growth.Predicting regulatory variants with composite statistic.Epigenomic mapping and effect sizes of noncoding variants associated with psychotropic drug response.GARLIC: a bioinformatic toolkit for aetiologically connecting diseases and cell type-specific regulatory maps.Enhancing the Promise of Drug Repositioning through Genetics.

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GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications.

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GWAS3D: Detecting human regula ...... ons and histone modifications.

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GWAS3D: Detecting human regula ...... ons and histone modifications.

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Junwen Wang

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Lily Yan Wang

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Mulin Jun Li

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Pak Chung Sham

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Zhengyuan Xia

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P2860

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

An integrated encyclopedia of DNA elements in the human genome

An integrated map of genetic variation from 1,092 human genomes

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

dbSNP: the NCBI database of genetic variation

Biological, clinical and population relevance of 95 loci for blood lipids

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

ORegAnno: an open-access community-driven resource for regulatory annotation

VISTA Enhancer Browser--a database of tissue-specific human enhancers

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