COMPUTER PROGRAM;
COPY NUMBER VARIATION;
DNA SEQUENCE;
GENETICS;
GENOME;
GENOMICS;
HETEROZYGOSITY LOSS;
HUMAN;
NEOPLASM;
PLOIDY;
PROCEDURES;
SINGLE NUCLEOTIDE POLYMORPHISM;
ARTICLE;
METHODOLOGY;
DNA COPY NUMBER VARIATIONS;
GENOME;
GENOMICS;
HUMANS;
LOSS OF HETEROZYGOSITY;
NEOPLASMS;
PLOIDIES;
POLYMORPHISM, SINGLE NUCLEOTIDE;
SEQUENCE ANALYSIS, DNA;
SOFTWARE DESIGN;
Control-FREEC: A tool for assessing copy number and allelic content using next-generation sequencing data
Boeva,V. et al. (2012) Control-FREEC: a tool for assessing copy number and allelic content using next-generation sequencing data. Bioinformatics, 28, 423-425.
Complete Genomics. (2012) http://www.completegenomics.com/public-data/ cancerdata/ (10 October 2011, date last accessed).
(2012)
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84867164956
Integrative analysis of genome-wide loss of heterozygosity and monoallelic expression at nucleotide resolution reveals disrupted pathways in triple-negative breast cancer
Ha,G. et al. (2012) Integrative analysis of genome-wide loss of heterozygosity and monoallelic expression at nucleotide resolution reveals disrupted pathways in triple-negative breast cancer. Genome Res., 22, 1995-2007.
A statistical approach for detecting genomic aberrations in heterogeneous tumor samples from single nucleotide polymorphism genotyping data
Yau,C. et al. (2010) A statistical approach for detecting genomic aberrations in heterogeneous tumor samples from single nucleotide polymorphism genotyping data. Genome Biol, 11, R92.
BIC-seq: A fast algorithm for detection of copy number alterations based on high-throughput sequencing data
Xi,R. et al. (2010) BIC-seq: a fast algorithm for detection of copy number alterations based on high-throughput sequencing data. Genome Biol., 11 (Suppl. 1), O10.