LOCAS--a low coverage assembly tool for resequencing projects
LOCAS--a low coverage assembly tool for resequencing projects
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Publisher
United States: Public Library of Science
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Language
English
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Publisher
United States: Public Library of Science
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Scope and Contents
Contents
Next Generation Sequencing (NGS) is a frequently applied approach to detect sequence variations between highly related genomes. Recent large-scale re-sequencing studies as the Human 1000 Genomes Project utilize NGS data of low coverage to afford sequencing of hundreds of individuals. Here, SNPs and micro-indels can be detected by applying an alignm...
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Full title
LOCAS--a low coverage assembly tool for resequencing projects
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TN_cdi_plos_journals_1307533637
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1307533637
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ISSN
1932-6203
E-ISSN
1932-6203
DOI
10.1371/journal.pone.0023455
