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Copy number variation detection in whole-genome sequencing data using the Bayesian information crite...

Copy number variation detection in whole-genome sequencing data using the Bayesian information crite...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_crossref_primary_10_1073_pnas_1110574108

Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion

About this item

Full title

Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion

Publisher

United States: National Academy of Sciences

Journal title

Proceedings of the National Academy of Sciences - PNAS, 2011-11, Vol.108 (46), p.E1128-E1136

Language

English

Formats

Publication information

Publisher

United States: National Academy of Sciences

More information

Scope and Contents

Contents

DNA copy number variations (CNVs) play an important role in the pathogenesis and progression of cancer and confer susceptibility to a variety of human disorders. Array comparative genomic hybridization has been used widely to identify CNVs genome wide, but the next-generation sequencing technology provides an opportunity to characterize CNVs genome...

Alternative Titles

Full title

Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_crossref_primary_10_1073_pnas_1110574108

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_crossref_primary_10_1073_pnas_1110574108

Other Identifiers

ISSN

0027-8424

E-ISSN

1091-6490

DOI

10.1073/pnas.1110574108

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