Using XHMM software to detect copy number variation in whole-exome sequencing data

Current Protocols in Human Genetics

Volumn , Issue SUPPL.81, 2014, Pages

  Fromer, Menachem ^a,b,c   Purcell, Shaun M ^a,b,c  

^a MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^b BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^c MASSACHUSETTS GENERAL HOSPITAL   (United States)

Author keywords

Copy number variation (CNV); Data normalization; Hidden markov model (HMM); Next generation sequencing (NGS); Principal component analysis (PCA)

Indexed keywords

COPY NUMBER VARIATION; EXOME; SOFTWARE;

DNA COPY NUMBER VARIATIONS; EXOME; SOFTWARE;

EID: 84905694066     PISSN: 19348266     EISSN: 19348258     Source Type: Journal    
DOI: 10.1002/0471142905.hg0723s81     Document Type: Article

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