SNP-sites: rapid efficient extraction of SNPs from multi-FASTA alignments
Rapidly decreasing genome sequencing costs have led to a proportionate increase in the number of samples used in prokaryotic population studies. Extracting single nucleotide polymorphisms (SNPs) from a large whole genome alignment is now a routine task, but existing tools have failed to scale effici...
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Published in | Microbial genomics Vol. 2; no. 4; p. e000056 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Microbiology Society
01.04.2016
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Subjects | |
Online Access | Get full text |
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Summary: | Rapidly decreasing genome sequencing costs have led to a proportionate increase in the number of samples used in prokaryotic population studies. Extracting single nucleotide polymorphisms (SNPs) from a large whole genome alignment is now a routine task, but existing tools have failed to scale efficiently with the increased size of studies. These tools are slow, memory inefficient and are installed through non-standard procedures. We present
SNP-sites
which can rapidly extract SNPs from a multi-FASTA alignment using modest resources and can output results in multiple formats for downstream analysis. SNPs can be extracted from a 8.3 GB alignment file (1842 taxa, 22 618 sites) in 267 seconds using 59 MB of RAM and 1 CPU core, making it feasible to run on modest computers. It is easy to install through the Debian and Homebrew package managers, and has been successfully tested on more than 20 operating systems.
SNP-sites
is implemented in C and is available under the open source license GNU GPL version 3. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 All supporting data, code and protocols have been provided within the article or through supplementary data files. |
ISSN: | 2057-5858 2057-5858 |
DOI: | 10.1099/mgen.0.000056 |