Literature DB >> 21828086

Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV.

Jarupon Fah Sathirapongsasuti1, Hane Lee, Basil A J Horst, Georg Brunner, Alistair J Cochran, Scott Binder, John Quackenbush, Stanley F Nelson.   

Abstract

MOTIVATION: The ability to detect copy-number variation (CNV) and loss of heterozygosity (LOH) from exome sequencing data extends the utility of this powerful approach that has mainly been used for point or small insertion/deletion detection.
RESULTS: We present ExomeCNV, a statistical method to detect CNV and LOH using depth-of-coverage and B-allele frequencies, from mapped short sequence reads, and we assess both the method's power and the effects of confounding variables. We apply our method to a cancer exome resequencing dataset. As expected, accuracy and resolution are dependent on depth-of-coverage and capture probe design. AVAILABILITY: CRAN package 'ExomeCNV'. CONTACT: fsathira@fas.harvard.edu; snelson@ucla.edu SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Entities:  

Mesh:

Year:  2011        PMID: 21828086      PMCID: PMC3179661          DOI: 10.1093/bioinformatics/btr462

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  31 in total

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7.  Origins and functional impact of copy number variation in the human genome.

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Authors:  F-Y Deng; L-J Zhao; Y-F Pei; B-Y Sha; X-G Liu; H Yan; L Wang; T-L Yang; R R Recker; C J Papasian; H-W Deng
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9.  DNA sequence capture and enrichment by microarray followed by next-generation sequencing for targeted resequencing: neurofibromatosis type 1 gene as a model.

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Journal:  Hum Mol Genet       Date:  2009-12-05       Impact factor: 6.150

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  198 in total

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5.  Using XHMM Software to Detect Copy Number Variation in Whole-Exome Sequencing Data.

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Journal:  Curr Protoc Hum Genet       Date:  2014-04-24

Review 6.  Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches.

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Journal:  Cancer Genet       Date:  2013-11-20

7.  Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives.

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Journal:  BMC Bioinformatics       Date:  2013-09-13       Impact factor: 3.169

8.  CANOES: detecting rare copy number variants from whole exome sequencing data.

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9.  Pan-cancer analysis of the extent and consequences of intratumor heterogeneity.

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10.  BubbleTree: an intuitive visualization to elucidate tumoral aneuploidy and clonality using next generation sequencing data.

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Journal:  Nucleic Acids Res       Date:  2015-11-17       Impact factor: 16.971

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