메뉴 건너뛰기




Volumn 29, Issue 19, 2013, Pages 2482-2484

OncoSNP-SEQ: A statistical approach for the identification of somatic copy number alterations from next-generation sequencing of cancer genomes

Author keywords

[No Author keywords available]

Indexed keywords

COMPUTER PROGRAM; COPY NUMBER VARIATION; DNA SEQUENCE; GENETICS; GENOME; GENOMICS; HETEROZYGOSITY LOSS; HUMAN; NEOPLASM; PLOIDY; PROCEDURES; SINGLE NUCLEOTIDE POLYMORPHISM; ARTICLE; METHODOLOGY;

EID: 84890189765     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/btt416     Document Type: Article
Times cited : (38)

References (9)
  • 1
    • 84859169877 scopus 로고    scopus 로고
    • The Cancer Cell Line Encyclopaedia enables predictive modelling of anticancer drug sensitivity
    • Barretina,J. et al. (2012) The Cancer Cell Line Encyclopaedia enables predictive modelling of anticancer drug sensitivity. Nature, 483, 603-607.
    • (2012) Nature , vol.483 , pp. 603-607
    • Barretina, J.1
  • 2
    • 77249119762 scopus 로고    scopus 로고
    • The landscape of somatic copy-number alteration across human cancers
    • Beroukhim,R. et al. (2010) The landscape of somatic copy-number alteration across human cancers. Nature, 463, 899-905.
    • (2010) Nature , vol.463 , pp. 899-905
    • Beroukhim, R.1
  • 3
    • 84856561659 scopus 로고    scopus 로고
    • 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.
    • (2012) Bioinformatics , vol.28 , pp. 423-425
    • Boeva, V.1
  • 4
    • 84868201489 scopus 로고    scopus 로고
    • What are we learning from the cancer genome? Nat
    • Collisson,E.A. et al. (2012)What are we learning from the cancer genome? Nat. Rev. Clin. Oncol., 9, 621-630.
    • (2012) Rev. Clin. Oncol. , vol.9 , pp. 621-630
    • Collisson, E.A.1
  • 5
    • 84898625550 scopus 로고    scopus 로고
    • (10 October 2011, date last accessed)
    • Complete Genomics. (2012) http://www.completegenomics.com/public-data/ cancerdata/ (10 October 2011, date last accessed).
    • (2012)
  • 6
    • 84867164956 scopus 로고    scopus 로고
    • 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.
    • (2012) Genome Res. , vol.22 , pp. 1995-2007
    • Ha, G.1
  • 7
    • 84869753284 scopus 로고    scopus 로고
    • Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns
    • Schuh,A. et al. (2012) Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns. Blood, 120, 4191-4196.
    • (2012) Blood , vol.120 , pp. 4191-4196
    • Schuh, A.1
  • 8
    • 77956690576 scopus 로고    scopus 로고
    • 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.
    • (2010) Genome Biol , vol.11
    • Yau, C.1
  • 9
    • 84893406680 scopus 로고    scopus 로고
    • 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.
    • (2010) Genome Biol. , vol.11 , Issue.SUPPL. 1
    • Xi, R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.