Log in to save to my catalogue

Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing

Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1989022859

Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing

About this item

Full title

Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing

Publisher

United States: Public Library of Science

Journal title

PloS one, 2018-01, Vol.13 (1), p.e0190264-e0190264

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Technological innovation and increased affordability have contributed to the widespread adoption of genome sequencing technologies in biomedical research. In particular large cancer research consortia have embraced next generation sequencing, and have used the technology to define the somatic mutation landscape of multiple cancer types. These studi...

Alternative Titles

Full title

Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1989022859

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1989022859

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0190264

How to access this item