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A combined reference panel from the 1000 Genomes and UK10K projects improved rare variant imputation...

A combined reference panel from the 1000 Genomes and UK10K projects improved rare variant imputation...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5177868

A combined reference panel from the 1000 Genomes and UK10K projects improved rare variant imputation in European and Chinese samples

About this item

Full title

A combined reference panel from the 1000 Genomes and UK10K projects improved rare variant imputation in European and Chinese samples

Publisher

London: Nature Publishing Group UK

Journal title

Scientific reports, 2016-12, Vol.6 (1), p.39313-39313, Article 39313

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Imputation using the 1000 Genomes haplotype reference panel has been widely adapted to estimate genotypes in genome wide association studies. To evaluate imputation quality with a relatively larger reference panel and a reference panel composed of different ethnic populations, we conducted imputations in the Framingham Heart Study and the North Chi...

Alternative Titles

Full title

A combined reference panel from the 1000 Genomes and UK10K projects improved rare variant imputation in European and Chinese samples

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5177868

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5177868

Other Identifiers

ISSN

2045-2322

E-ISSN

2045-2322

DOI

10.1038/srep39313

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