Amplification and thrifty single-molecule sequencing of recurrent somatic structural variations

Genome Research

Volumn 24, Issue 2, 2014, Pages 318-328

  Patel, Anand ^a   Schwab, Richard ^b   Liu, Yu Tsueng ^b   Bafna, Vineet ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TUMOR MARKER;

AMPLICON; ARTICLE; CANCER CELL CULTURE; CANCER PATIENT; CDKN2A GENE; CONTROLLED STUDY; DNA HYBRIDIZATION; DNA STRAND BREAKAGE; FUSION GENE; GENE AMPLIFICATION; GENE DELETION; GENE REARRANGEMENT; GENE SEQUENCE; GENE TRANSLOCATION; GENETIC VARIABILITY; GERM LINE; HEMATOLOGIC MALIGNANCY; HUMAN; HUMAN CELL; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RUNX1 RUNX1T1 FUSION GENE; SIMULATION; SOLID TUMOR; TUMOR SUPPRESSOR GENE;

ALGORITHMS; CHROMOSOME ABERRATIONS; CHROMOSOME BREAKPOINTS; CYCLIN-DEPENDENT KINASE INHIBITOR P16; EXOME; GENOME, HUMAN; GENOMIC STRUCTURAL VARIATION; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MCF-7 CELLS; NEOPLASMS; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS, DNA; SEQUENCE DELETION; TRANSLOCATION, GENETIC;

EID: 84893641770     PISSN: 10889051     EISSN: 15495469     Source Type: Journal    
DOI: 10.1101/gr.161497.113     Document Type: Article

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