ABC: A tool to identify SNVs causing allele-specific transcription factor binding from ChIP-Seq experiments

Bioinformatics

Volumn 31, Issue 18, 2015, Pages 3057-3059

  Bailey, Swneke D ^a,b   Virtanen, Carl ^a   Haibe Kains, Benjamin ^a,b   Lupien, Mathieu ^a,b,c  

^a PRINCESS MARGARET HOSPITAL   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c ONTARIO INSTITUTE FOR CANCER RESEARCH   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMATIN; FOXA1 PROTEIN, HUMAN; HEPATOCYTE NUCLEAR FACTOR 3ALPHA; PROTEIN BINDING; TRANSCRIPTION FACTOR;

ALGORITHM; ALLELE; BIOLOGY; BREAST TUMOR; CHROMATIN; CHROMATIN IMMUNOPRECIPITATION; FEMALE; GENETICS; HIGH THROUGHPUT SEQUENCING; HUMAN; METABOLISM; MUTATION; PROCEDURES; PROMOTER REGION; SINGLE NUCLEOTIDE POLYMORPHISM;

ALGORITHMS; ALLELES; BREAST NEOPLASMS; CHROMATIN; CHROMATIN IMMUNOPRECIPITATION; COMPUTATIONAL BIOLOGY; FEMALE; HEPATOCYTE NUCLEAR FACTOR 3-ALPHA; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; PROMOTER REGIONS, GENETIC; PROTEIN BINDING; TRANSCRIPTION FACTORS;

EID: 84941756599     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/btv321     Document Type: Article

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