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Genome structural variation discovery and genotyping

Genome structural variation discovery and genotyping

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4108431

Genome structural variation discovery and genotyping

About this item

Full title

Genome structural variation discovery and genotyping

Publisher

London: Nature Publishing Group UK

Journal title

Nature reviews. Genetics, 2011-05, Vol.12 (5), p.363-376

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Key Points
Structural variation was originally defined as insertions, deletions and inversions greater than 1 kb in size, but with the sequencing of human genomes now becoming routine, the operational spectrum of structural variants has widened to include events >50 bp in length.
The main focus of structural variant (SV) studies should be acc...

Alternative Titles

Full title

Genome structural variation discovery and genotyping

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4108431

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4108431

Other Identifiers

ISSN

1471-0056

E-ISSN

1471-0064

DOI

10.1038/nrg2958

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