Case study of sequence capture enrichment technology: Identification of variation underpinning developmental syndromes in an amniote model

Genes

Volumn 3, Issue 2, 2012, Pages 233-247

  Robb, Elizabeth A ^a   Delany, Mary E ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Bioinformatics; Capture array; Chicken; Congenic; Indel; Mutation; Next generation sequencing; SNP; Variant

Indexed keywords

AMNIOTE; ANIMAL TISSUE; ARTICLE; BIRD; CHROMOSOME MAP; CONGENIC STRAIN; DEVELOPMENT; DEVELOPMENTAL DISORDER; EMBRYO; FEMALE; GENE MUTATION; GENE REARRANGEMENT; GENE SEQUENCE; GENE TECHNOLOGY; GENOME; INDEL MUTATION; MALE; MUTANT; NEXT GENERATION SEQUENCING; NONHUMAN; ORGANOGENESIS; SEQUENCE ALIGNMENT; SEQUENCE CAPTURE ENRICHMENT TECHNOLOGY; SINGLE NUCLEOTIDE POLYMORPHISM; VERTEBRATE;

AVES; VERTEBRATA;

EID: 84863314405     PISSN: None     EISSN: 20734425     Source Type: Journal    
DOI: 10.3390/genes3020233     Document Type: Article

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