In-depth annotation of SNPs arising from resequencing projects using NGS-SNP.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 21697123.
- Also identified by DOI 10.1093/bioinformatics/btr372 and PMC identifier 3150039.
- Licence recorded as CC BY-NC.
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Abstract
NGS-SNP is a collection of command-line scripts for providing rich annotations for SNPs identified by the sequencing of whole genomes from any organism with reference sequences in Ensembl. Included among the annotations, several of which are not available from any existing SNP annotation tools, are the results of detailed comparisons with orthologous sequences. These comparisons can, for example, identify SNPs that affect conserved residues, or alter residues or genes linked to phenotypes in another species. NGS-SNP is available both as a set of scripts and as a virtual machine. The virtual machine consists of a Linux operating system with all the NGS-SNP dependencies pre-installed. The source code and virtual machine are freely available for download at http://stothard.afns.ualberta.ca/downloads/NGS-SNP/. stothard@ualberta.ca Supplementary data are available at Bioinformatics online.
Medical subject headings
- High-Throughput Nucleotide Sequencing
- Molecular Sequence Annotation
- Polymorphism, Single Nucleotide