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
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Publisher
England: Nature Publishing Group
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English
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Publisher
England: Nature Publishing Group
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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...
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Population-specific genetic variation in large sequencing data sets: why more data is still better
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5602011
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5602011
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ISSN
1018-4813
E-ISSN
1476-5438
DOI
10.1038/ejhg.2017.110