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Population-specific genetic variation in large sequencing data sets: why more data is still better

Population-specific genetic variation in large sequencing data sets: why more data is still better

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5602011

Population-specific genetic variation in large sequencing data sets: why more data is still better

About this item

Full title

Population-specific genetic variation in large sequencing data sets: why more data is still better

Publisher

England: Nature Publishing Group

Journal title

European journal of human genetics : EJHG, 2017-10, Vol.25 (10), p.1173-1175

Language

English

Formats

Publication information

Publisher

England: Nature Publishing Group

More information

Scope and Contents

Contents

We have generated a next-generation whole-exome sequencing data set of 2628 participants of the population-based Rotterdam Study cohort, comprising 669 737 single-nucleotide variants and 24 019 short insertions and deletions. Because of broad and deep longitudinal phenotyping of the Rotterdam Study, this data set permits extensive interpretation of...

Alternative Titles

Full title

Population-specific genetic variation in large sequencing data sets: why more data is still better

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5602011

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5602011

Other Identifiers

ISSN

1018-4813

E-ISSN

1476-5438

DOI

10.1038/ejhg.2017.110

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