A Streamlined Method for Detecting Structural Variants in Cancer Genomes by Short Read Paired-End Sequencing

PLoS ONE

Volumn 7, Issue 10, 2012, Pages

  Mijušković, Martina ^a   Brown, Stuart M ^b   Tang, Zuojian ^b   Lindsay, Cory R ^a   Efstathiadis, Efstratios ^b   Deriano, Ludovic ^c,d   Roth, David B ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b NEW YORK UNIVERSITY MEDICAL CENTER   (United States)

^c INSTITUT PASTEUR   (France)

^d CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CANCER GENOME; CHROMOSOME INVERSION; COMPUTER PROGRAM; CONTROLLED STUDY; FALSE POSITIVE RESULT; GENE DELETION; GENE DUPLICATION; GENE IDENTIFICATION; GENE REARRANGEMENT; GENE TRANSLOCATION; GENETIC VARIABILITY; GENOME; MOUSE; NONHUMAN; ONCOGENE; STREAMLINED METHOD; T CELL LYMPHOMA;

ANIMALS; CHROMOSOME ABERRATIONS; CHROMOSOME MAPPING; COMPUTATIONAL BIOLOGY; DNA-BINDING PROTEINS; GENOME; GENOMICS; HUMANS; LYMPHOMA, T-CELL; MICE; MICE, 129 STRAIN; MICE, INBRED C57BL; MICE, KNOCKOUT; MUTATION; NEOPLASMS; REPRODUCIBILITY OF RESULTS; SENSITIVITY AND SPECIFICITY; SEQUENCE ANALYSIS, DNA; SOFTWARE; TUMOR SUPPRESSOR PROTEIN P53;

EID: 84868118627     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0048314     Document Type: Article

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