Variant tool chest: An improved tool to analyze and manipulate variant call format (VCF) files

BMC Bioinformatics

Volumn 15, Issue , 2014, Pages 1-5

  Ebbert, Mark T W ^a,b   Wadsworth, Mark E ^a   Boehme, K L ^a   Hoyt, Kaitlyn L ^a   Sharp, Aaron R ^a   O'Fallon, Brendan D ^b   Kauwe, John S K ^a   Ridge, Perry G ^a  

^a BRIGHAM YOUNG UNIVERSITY   (United States)

^b ARUP INSTITUTE FOR CLINICAL AND EXPERIMENTAL PATHOLOGY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOMES;

COMMUNITY STANDARDS; DIVERSE FIELDS; GENETIC VARIANTS; INSERTIONS AND DELETIONS; MEDICAL GENETICS; NEXT-GENERATION SEQUENCING; PHYLOGENETICS; SINGLE NUCLEOTIDES;

PATHOLOGY;

CAUCASIAN; GENOME; HUMAN; INDEL MUTATION; SINGLE NUCLEOTIDE POLYMORPHISM; SOFTWARE; THORAX; ARTICLE; COMPUTER PROGRAM; GENETIC DATABASE; GENETIC VARIABILITY; GENOTYPE; HIGH THROUGHPUT SEQUENCING; HUMAN GENOME; METHODOLOGY;

DATABASES, GENETIC; GENETIC VARIATION; GENOME, HUMAN; GENOTYPE; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; SOFTWARE;

EID: 84988360744     PISSN: None     EISSN: 14712105     Source Type: Journal    
DOI: 10.1186/1471-2105-15-S7-S12     Document Type: Article

References (6)

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