Distinguishing somatic and germline copy number events in cancer patient DNA hybridized to whole-genome SNP genotyping arrays

Methods in Molecular Biology

Volumn 973, Issue , 2013, Pages 355-372

  Ha, Gavin ^a   Shah, Sohrab ^a  

^a NONE

Author keywords

Affymetrix Genome Wide Human SNP6.0; Cancer SNP genotyping array data; Copy number alterations; Germline copy number variants; High density SNP genotyping arrays; HMM Dosage; Illumina Human1M BeadChip; Probabilistic

Indexed keywords

DNA;

ALGORITHM; ARTICLE; BREAST CANCER; CANCER CELL; CANCER PATIENT; COPY NUMBER VARIATION; DNA HYBRIDIZATION; GENE FREQUENCY; GENOME; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; COMPUTER PROGRAM; DNA MICROARRAY; GENE DOSAGE; GENETICS; GENOTYPING TECHNIQUE; METHODOLOGY; NEOPLASM; PROBABILITY;

DNA; DNA COPY NUMBER VARIATIONS; GENE DOSAGE; GENOTYPING TECHNIQUES; HUMANS; NEOPLASMS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; PROBABILITY; SOFTWARE;

MLCS; MLOWN;

EID: 84880799426     PISSN: 10643745     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-62703-281-0_22     Document Type: Article

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