Quantification of rare allelic variants from pooled genomic DNA
Quantification of rare allelic variants from pooled genomic DNA
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Publisher
New York: Nature Publishing Group US
Journal title
Language
English
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Publisher
New York: Nature Publishing Group US
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Scope and Contents
Contents
The base-calling algorithm SNPSeeker detects single-nucleotide polymorphisms with frequencies that are below the error rate of the sequencing platform. It is thus well suited to analyze data from large pooled samples and find rare variants that may contribute to diseases or complex traits.
We report a targeted, cost-effective method to quantify...
Alternative Titles
Full title
Quantification of rare allelic variants from pooled genomic DNA
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2776647
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2776647
Other Identifiers
ISSN
1548-7091
E-ISSN
1548-7105
DOI
10.1038/nmeth.1307
