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Towards a comprehensive structural variation map of an individual human genome

Towards a comprehensive structural variation map of an individual human genome

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_DiVA_org_uu_135831

Towards a comprehensive structural variation map of an individual human genome

About this item

Full title

Towards a comprehensive structural variation map of an individual human genome

Publisher

England: BioMed Central Ltd

Journal title

Genome Biology (Online Edition), 2010-05, Vol.11 (5), p.R52-2345, Article R52

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Several genomes have now been sequenced, with millions of genetic variants annotated. While significant progress has been made in mapping single nucleotide polymorphisms (SNPs) and small (<10 bp) insertion/deletions (indels), the annotation of larger structural variants has been less comprehensive. It is still unclear to what extent a typical genom...

Alternative Titles

Full title

Towards a comprehensive structural variation map of an individual human genome

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_swepub_primary_oai_DiVA_org_uu_135831

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_DiVA_org_uu_135831

Other Identifiers

ISSN

1474-760X,1474-7596

E-ISSN

1474-760X

DOI

10.1186/gb-2010-11-5-r52

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