Exome sequencing reveals comprehensive genomic alterations across eight cancer cell lines

PLoS ONE

Volumn 6, Issue 6, 2011, Pages

  Chang, Han ^a   Jackson, Donald G ^a   Kayne, Paul S ^a   Ross Macdonald, Petra B ^a   Ryseck, Rolf Peter ^a   Siemers, Nathan O ^a  

^a BRISTOL MYERS SQUIBB   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACCURACY; ARTICLE; BREAST CANCER; CANCER CELL CULTURE; CARCINOGENESIS; COLON CANCER; CONTROLLED STUDY; DISEASE COURSE; EXOME; GENE AMPLIFICATION; GENE DELETION; GENE MUTATION; GENETIC DATABASE; GENETIC VARIABILITY; HUMAN; LUNG CANCER; MALIGNANT NEOPLASTIC DISEASE; OVARY CANCER; PROSTATE CANCER; RELIABILITY; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY; SINGLE NUCLEOTIDE POLYMORPHISM; SOFT TISSUE CANCER; STOMACH CANCER; TREATMENT OUTCOME; TUMOR GENE; DNA SEQUENCE; EXON; GENETICS; GENOTYPE; HIGH THROUGHPUT SEQUENCING; HUMAN GENOME; MUTATION; NEOPLASM; TUMOR CELL LINE;

CELL LINE, TUMOR; EXONS; GENOME, HUMAN; GENOTYPE; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MUTATION; NEOPLASMS; SEQUENCE ANALYSIS, DNA;

EID: 79959311118     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0021097     Document Type: Article

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