BlackOPs: Increasing confidence in variant detection through mappability filtering

Nucleic Acids Research

Volumn 41, Issue 19, 2013, Pages

  Cabanski, Christopher R ^a,b   Wilkerson, Matthew D ^c,d   Soloway, Matthew ^c   Parker, Joel S ^c,d   Liu, Jinze ^e   Prins, Jan F ^f   Marron, J S ^a,c   Perou, Charles M ^c,d   Neil Hayes, D ^c,d  

^a University of North Carolina at Chapel Hill   (United States)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF NORTH CAROLINA   (United States)

^d UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^e UNIVERSITY OF KENTUCKY   (United States)

^f Brooks Computer Science Building   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; COMPUTER PROGRAM; COMPUTER SIMULATION; CONTROLLED STUDY; EXON; GENE EXPRESSION PROFILING; GENE INSERTION; GENE MAPPING; GENETIC ANALYSIS; GENETIC DATABASE; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; HETEROZYGOSITY; HIGH THROUGHPUT SEQUENCING; HOMOZYGOSITY; HUMAN; HUMAN CELL; PRIORITY JOURNAL; SEQUENCE ALIGNMENT; SINGLE NUCLEOTIDE POLYMORPHISM;

ARTIFACTS; CELL LINE, TUMOR; CHROMOSOME MAPPING; DATABASES, NUCLEIC ACID; EXOME; GENETIC VARIATION; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS, DNA; SEQUENCE ANALYSIS, RNA; SOFTWARE;

EID: 84886058564     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkt692     Document Type: Article

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