Abstract
AutoSNP is a program to detect single nucleotide polymorphisms (SNPs) and insertion/deletion polymorphisms (indels) in expressed sequence tag (EST) data. The program uses d2cluster and cap3 to cluster and align EST sequences, and uses redundancy to differentiate between candidate SNPs and sequence errors. Candidate polymorphisms are identified as occurring in multiple reads within an alignment. For each candidate SNP, two measures of confidence are calculated, the redundancy of the polymorphism at a SNP locus and the co segregation of the candidate SNP with other SNPs in the alignment.
Cite
CITATION STYLE
Barker, G., Batley, J., O’Sullivan, H., Edwards, K. J., & Edwards, D. (2003). Redundancy based detection of sequence polymorphisms in expressed sequence tag data using autoSNP. Bioinformatics, 19(3), 421–422. https://doi.org/10.1093/bioinformatics/btf881
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.