SAMFIRE: multi-locus variant calling for time-resolved sequence data.
basic_science · Level V
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- Record sourced from PubMed, PMID 27153641.
- Also identified by DOI 10.1093/bioinformatics/btw205 and PMC identifier 4937198.
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Abstract
An increasingly common method for studying evolution is the collection of time-resolved short-read sequence data. Such datasets allow for the direct observation of rapid evolutionary processes, as might occur in natural microbial populations and in evolutionary experiments. In many circumstances, evolutionary pressure acting upon single variants can cause genomic changes at multiple nearby loci. SAMFIRE is an open-access software package for processing and analyzing sequence reads from time-resolved data, calling important single- and multi-locus variants over time, identifying alleles potentially affected by selection, calculating linkage disequilibrium statistics, performing haplotype reconstruction and exploiting time-resolved information to estimate the extent of uncertainty in reported genomic data. C ++ code may be found at https://github.com/cjri/samfire/ chris.illingworth@gen.cam.ac.uk Supplementary data are available at Bioinformatics online.
Medical subject headings
- Genomics
- Sequence Analysis, DNA
- Software