| Literature DB >> 35612753 |
Pavel Sinitcyn1, Maximilian Gerwien1, Jürgen Cox2.
Abstract
Standard shotgun proteomics data analysis pipelines usually only identify peptides that are encoded in the reference genome. In many situations, it is desirable to identify peptides resulting from non-synonymous variations as well. Here, we present a new module in the MaxQuant software that takes both DNA and RNA based next-generation sequencing (NGS) data as well as raw proteomics data as input. This allows for the identification of variant peptides that are otherwise missed.Entities:
Keywords: Immunopeptidomics; MaxQuant; NGS; Proteogenomics; Proteomics; Sequence variations
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Year: 2022 PMID: 35612753 DOI: 10.1007/978-1-0716-2124-0_23
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745