Improved Variant Calling Accuracy by Merging Replicates in Whole-Exome Sequencing Studies

BioMed Research International

Volumn 2014, Issue , 2014, Pages

  Zhang, Yanfeng ^a   Li, Bingshan ^a   Li, Chun ^b   Cai, Qiuyin ^a   Zheng, Wei ^a   Long, Jirong ^a  

^a VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^b VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; COMPARATIVE STUDY; EXOME; GENE CLUSTER; GENE DUPLICATION; GENE FREQUENCY; GENE MAPPING; GENE SEQUENCE; GENETIC PARAMETERS; GENETIC VARIABILITY; GENOME; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN GENOME PROJECT; POPULATION BASED CASE CONTROL STUDY; SINGLE NUCLEOTIDE POLYMORPHISM; TIME; WHOLE EXOME SEQUENCING; DNA SEQUENCE; GENETICS; HIGH THROUGHPUT SEQUENCING; PROCEDURES;

EXOME; GENOTYPE; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, DNA;

EID: 84930187334     PISSN: 23146133     EISSN: 23146141     Source Type: Journal    
DOI: 10.1155/2014/319534     Document Type: Article

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