Annotation of functional variation in personal genomes using RegulomeDB - Wikidata - wikimedia - TriplyDB

Annotation of functional variation in personal genomes using RegulomeDB

Annotation of functional variation in personal genomes using RegulomeDB

http://www.wikidata.org/entity/Q29614867

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What does our genome encode?An integrated encyclopedia of DNA elements in the human genome Genetic variants within the MHC region are associated with immune responsiveness to childhood vaccinations Genetic variants in the major histocompatibility complex class I and class II genes are associated with diisocyanate-induced asthma N-acetyltransferase 2 genotypes are associated with diisocyanate-induced asthma Genetic variants in TNFa, TGFB1, PTGS1 and PTGS2 genes are associated with diisocyanate-induced asthma Imputation and subset based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma Gene Prioritization for Imaging Genetics Studies Using Gene Ontology and a Stratified False Discovery Rate Approach Association of gamma-aminobutyric acid A receptor α2 gene (GABRA2) with alcohol use disorder Analysis of Genomic Sequence Motifs for Deciphering Transcription Factor Binding and Transcriptional Regulation in Eukaryotic Cells Making sense of GWAS: using epigenomics and genome engineering to understand the functional relevance of SNPs in non-coding regions of the human genome The search for cis-regulatory driver mutations in cancer genomes The epigenome, 4D nucleome and next-generation neuropsychiatric pharmacogenomics The impact of next-generation sequencing technologies on HLA research High-throughput sequencing for biology and medicine Candidate gene association studies: a comprehensive guide to useful in silico tools Rare-variant association analysis: study designs and statistical tests Using the ENCODE Resource for Functional Annotation of Genetic Variants A review of post-GWAS prioritization approaches A brief review on the Human Encyclopedia of DNA Elements (ENCODE) project Neurogenomics of speech and language disorders: the road ahead Enhancer scanning to locate regulatory regions in genomic loci DNA variants in CACNA1C modify Parkinson disease risk only when vitamin D level is deficient.Genetic basis of irritant susceptibility in health care workers Association of MHC region SNPs with irritant susceptibility in healthcare workers Identification and utilization of donor and recipient genetic variants to predict survival after HCT: are we ready for primetime?Progress in understanding the genomic basis for adverse drug reactions: a comprehensive review and focus on the role of ethnicity Capture Hi-C identifies a novel causal gene, IL20RA, in the pan-autoimmune genetic susceptibility region 6q23 Genome-wide association study reveals two new risk loci for bipolar disorder Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error Expression of phosphofructokinase in skeletal muscle is influenced by genetic variation and associated with insulin sensitivity Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk Identification of epidermal growth factor receptor (EGFR) genetic variants that modify risk for head and neck squamous cell carcinoma Pedigree based DNA sequencing pipeline for germline genomes of cancer families TERT gene harbors multiple variants associated with pancreatic cancer susceptibility Deciphering associations for lung cancer risk through imputation and analysis of 12,316 cases and 16,831 controls Systematic genetic analysis identifies Cis-eQTL target genes associated with glioblastoma patient survival

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P2860

Annotation of functional variation in personal genomes using RegulomeDB

http://www.wikidata.org/entity/Q29614867

description

2012 nî lūn-bûn

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2012 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2012年の論文

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2012年論文

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2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

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2012年论文

@wuu

name

Annotation of functional variation in personal genomes using RegulomeDB

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Annotation of functional variation in personal genomes using RegulomeDB

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type

label

Annotation of functional variation in personal genomes using RegulomeDB

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Annotation of functional variation in personal genomes using RegulomeDB

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Annotation of functional variation in personal genomes using RegulomeDB

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Annotation of functional variation in personal genomes using RegulomeDB

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Genome Research

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Annotation of functional variation in personal genomes using RegulomeDB

@en

P2093

Benjamin C Hitz

http://www.w3.org/2001/XMLSchema#string

Eurie L Hong

http://www.w3.org/2001/XMLSchema#string

Julie Park

http://www.w3.org/2001/XMLSchema#string

Manoj Hariharan

http://www.w3.org/2001/XMLSchema#string

Marc A Schaub

http://www.w3.org/2001/XMLSchema#string

Maya Kasowski

http://www.w3.org/2001/XMLSchema#string

Michael Snyder

http://www.w3.org/2001/XMLSchema#string

Shuai Weng

http://www.w3.org/2001/XMLSchema#string

Yong Cheng

http://www.w3.org/2001/XMLSchema#string

P2860

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

Model-based analysis of ChIP-Seq (MACS)

Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain

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

Finding the missing heritability of complex diseases

Genome-wide promoter analysis of the SOX4 transcriptional network in prostate cancer cells

Differential genomic targeting of the transcription factor TAL1 in alternate haematopoietic lineages

TRANSFAC and its module TRANSCompel: transcriptional gene regulation in eukaryotes

GENCODE: the reference human genome annotation for The ENCODE Project

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1790-1797

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scholarly article

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190915

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10.1101/GR.137323.112

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P433

9

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22

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Konrad J. Karczewski

J. Michael Cherry

Jakub Karczewski

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2012-09-01T00:00:00Z

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230811297

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22955989

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3431494

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