Single nucleotide variations (SNVs) located within a reading frame can result in single amino acid polymorphisms (SAPs), leading to alteration of the corresponding amino acid sequence as well as function of a protein. Accurate detection of SAPs is an important issue in proteomic analysis at the experimental and bioinformatic level. Herein, we present sapFinder, an R software package, for detection of the variant peptides based on tandem mass spectrometry (MS/MS)-based proteomics data. This package automates the construction of variation-associated databases from public SNV repositories or sample-specific next-generation sequencing (NGS) data and the identification of SAPs through database searching, post-processing and generation of HTML-based report with visualized interface.
CITATION STYLE
Wen, B., Xu, S., Sheynkman, G. M., Feng, Q., Lin, L., Wang, Q., … Liu, S. (2014). SapFinder: An R/Bioconductor package for detection of variant peptides in shotgun proteomics experiments. Bioinformatics, 30(21), 3136–3138. https://doi.org/10.1093/bioinformatics/btu397
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