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Exome capture from saliva produces high quality genomic and metagenomic data

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Title Exome capture from saliva produces high quality genomic and metagenomic data
Names Kidd, Jeffrey M. (creator)
Sharpton, Thomas J. (creator)
Bobo, Dean (creator)
Norman, Paul J. (creator)
Martin, Alicia R. (creator)
Carpenter, Meredith L. (creator)
Sikora, Martin (creator)
Gignoux, Christopher R. (creator)
Nemat-Gorgani, Neda (creator)
Adams, Alexandra (creator)
Guadalupe, Moraima (creator)
Guo, Xiaosen (creator)
Feng, Qiang (creator)
Li, Yingrui (creator)
Liu, Xiao (creator)
Parham, Peter (creator)
Hoal, Eileen G. (creator)
Feldman, Marcus W. (creator)
Pollard, Katherine S. (creator)
Wall, Jeffrey D. (creator)
Bustamante, Carlos D. (creator)
Henn, Brenna M. (creator)
Date Issued 2014-04-04 (iso8601)
Note This is the publisher’s final pdf. The published article is copyrighted by the author(s) and published by BioMed Central Ltd. The published article can be found at: http://www.biomedcentral.com/bmcgenomics.
Abstract BACKGROUND: Targeted capture of genomic regions reduces sequencing cost while generating higher coverage by
allowing biomedical researchers to focus on specific loci of interest, such as exons. Targeted capture also has the
potential to facilitate the generation of genomic data from DNA collected via saliva or buccal cells. DNA samples
derived from these cell types tend to have a lower human DNA yield, may be degraded from age and/or have
contamination from bacteria or other ambient oral microbiota. However, thousands of samples have been previously
collected from these cell types, and saliva collection has the advantage that it is a non-invasive and appropriate for a
wide variety of research.
RESULTS: We demonstrate successful enrichment and sequencing of 15 South African KhoeSan exomes and 2 full
genomes with samples initially derived from saliva. The expanded exome dataset enables us to characterize genetic
diversity free from ascertainment bias for multiple KhoeSan populations, including new exome data from six HGDP
Namibian San, revealing substantial population structure across the Kalahari Desert region. Additionally, we discover
and independently verify thirty-one previously unknown KIR alleles using methods we developed to accurately map
and call the highly polymorphic HLA and KIR loci from exome capture data. Finally, we show that exome capture of
saliva-derived DNA yields sufficient non-human sequences to characterize oral microbial communities, including
detection of bacteria linked to oral disease (e.g. Prevotella melaninogenica). For comparison, two samples were
sequenced using standard full genome library preparation without exome capture and we found no systematic
bias of metagenomic information between exome-captured and non-captured data.
CONCLUSIONS: DNA from human saliva samples, collected and extracted using standard procedures, can be used to
successfully sequence high quality human exomes, and metagenomic data can be derived from non-human reads.
We find that individuals from the Kalahari carry a higher oral pathogenic microbial load than samples surveyed in
the Human Microbiome Project. Additionally, rare variants present in the exomes suggest strong population structure
across different KhoeSan populations.
Genre Article
Access Condition http://creativecommons.org/licenses/by/3.0/us/
Topic Exomes
Identifier Kidd et al.: Exome capture from saliva produces high quality genomic and metagenomic data. BMC Genomics 2014 15:262. doi:10.1186/1471-2164-15-262

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