Using ERDS to infer copy-number variants in high-coverage genomes

American Journal of Human Genetics

Volumn 91, Issue 3, 2012, Pages 408-421

  Zhu, Mingfu ^a   Need, Anna C ^a   Han, Yujun ^a   Ge, Dongliang ^a,b   Maia, Jessica M ^a   Zhu, Qianqian ^a,c   Heinzen, Erin L ^a   Cirulli, Elizabeth T ^a   Pelak, Kimberly ^a   He, Min ^a   Ruzzo, Elizabeth K ^a   Gumbs, Curtis ^a   Singh, Abanish ^a   Feng, Sheng ^b   Shianna, Kevin V ^a   Goldstein, David B ^a  

^a DUKE UNIVERSITY   (United States)

^b DUKE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c ROSWELL PARK CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANALYTIC METHOD; ARTICLE; COPY NUMBER VARIATION; ESTIMATION BY READ DEPTH WITH SINGLE NUCLEOTIDE VARIANT; FALSE POSITIVE RESULT; GENE DELETION; GENOTYPE; HETEROZYGOSITY; HUMAN; HUMAN GENOME; PREDICTIVE VALUE; PRIORITY JOURNAL; SENSITIVITY AND SPECIFICITY; SEQUENCE ALIGNMENT;

EID: 84866092268     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2012.07.004     Document Type: Article

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