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Genome variation discovery with high-throughput sequencing data

Genome variation discovery with high-throughput sequencing data

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_733850358

Genome variation discovery with high-throughput sequencing data

About this item

Full title

Genome variation discovery with high-throughput sequencing data

Publisher

England: Oxford University Press

Journal title

Briefings in bioinformatics, 2010-01, Vol.11 (1), p.3-14

Language

English

Formats

Publication information

Publisher

England: Oxford University Press

More information

Scope and Contents

Contents

The advent of high-throughput sequencing (HTS) technologies is enabling sequencing of human genomes at a significantly lower cost. The availability of these genomes is hoped to enable novel medical diagnostics and treatment, specific to the individual, thus launching the era of personalized medicine. The data currently generated by HTS machines req...

Alternative Titles

Full title

Genome variation discovery with high-throughput sequencing data

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_733850358

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_733850358

Other Identifiers

ISSN

1467-5463

E-ISSN

1477-4054

DOI

10.1093/bib/bbp058

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