Rare variant phasing and haplotypic expression from RNA sequencing with phASER

Nature Communications

Volumn 7, Issue , 2016, Pages

  Castel, Stephane E ^a,b   Mohammadi, Pejman ^a,b   Chung, Wendy K ^b   Shen, Yufeng ^b   Lappalainen, Tuuli ^a,b  

^a NEW YORK GENOME CENTER   (United States)

^b Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; DNA; GENE EXPRESSION; GENETIC ANALYSIS; GENETIC VARIATION; GENOME; GENOMICS; HETEROZYGOSITY; MOLECULAR ANALYSIS; RNA;

ACCURACY; ALLELE; ARTICLE; CHROMOSOME; CLINICAL ARTICLE; CONGENITAL DIAPHRAGM HERNIA; CONTROLLED STUDY; DNA SEQUENCE; EXON; FIBROBLAST; GENE EXPRESSION; GENE FREQUENCY; GENETIC ANALYSIS; GENETIC VARIABILITY; HAPLOTYPE; HETEROZYGOTE; HUMAN; LYMPHOBLASTOID CELL LINE; MEDICAL GENETICS; PHASER; QUANTITATIVE TRAIT LOCUS; RNA SEQUENCE; RNA SPLICING; GENETIC VARIATION; GENETICS; GENOME-WIDE ASSOCIATION STUDY; HIGH THROUGHPUT SEQUENCING; NUCLEOTIDE SEQUENCE; PROCEDURES; SEQUENCE ANALYSIS;

DNA; RNA;

BASE SEQUENCE; DNA; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; HAPLOTYPES; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; RNA; SEQUENCE ANALYSIS, DNA; SEQUENCE ANALYSIS, RNA;

EID: 84986587259     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms12817     Document Type: Article

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