Abstract
AbstractSearching tandem mass spectrometry proteomics data against a database is a well-established method for assigning peptide sequences to observed spectra but typically cannot identify peptides harboring unexpected post-translational modifications (PTMs). Open modification searching aims to address this problem by allowing a spectrum to match a peptide even if the spectrum’s precursor mass differs from the peptide mass. However, expanding the search space in this way can lead to a loss in statistical power to detect peptides. We therefore developed a method, called CONGA, that takes into account results from both types of searches—a traditional “narrow window” search and an open modification search—while carrying out rigorous false discovery rate (FDR) control. The result is an algorithm that provides the best of both worlds: the ability to detect unexpected PTMs without a concomitant loss of power to detect unmodified peptides.
Publisher
Cold Spring Harbor Laboratory
Cited by
3 articles.
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