Variant calling in low-coverage whole genome sequencing of a Native American population sample
Variant calling in low-coverage whole genome sequencing of a Native American population sample
About this item
Full title
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Publisher
England: BioMed Central Ltd
Journal title
Language
English
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Publication information
Publisher
England: BioMed Central Ltd
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Scope and Contents
Contents
The reduction in the cost of sequencing a human genome has led to the use of genotype sampling strategies in order to impute and infer the presence of sequence variants that can then be tested for associations with traits of interest. Low-coverage Whole Genome Sequencing (WGS) is a sampling strategy that overcomes some of the deficiencies seen in f...
Alternative Titles
Full title
Variant calling in low-coverage whole genome sequencing of a Native American population sample
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Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3914019
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3914019
Other Identifiers
ISSN
1471-2164
E-ISSN
1471-2164
DOI
10.1186/1471-2164-15-85
