{"title":"FineFDR: Fine-grained Taxonomy-specific False Discovery Rates Control in Metaproteomics.","authors":"Shengze Wang, Shichao Feng, Chongle Pan, Xuan Guo","doi":"10.1109/bibm55620.2022.9995401","DOIUrl":null,"url":null,"abstract":"<p><p>Microbial community proteomics, also termed metaproteomics, investigates all proteins expressed by a microbiota. Tandem mass spectrometry (MS/MS) is the typical method for identifying proteins in metaproteomics, which involves searching the mass spectra against a protein sequence database. A major post-analysis step is controlling the false discovery rate (FDR), i.e., the ratio of false positives to the total number of annotations. The current popular target-decoy FDR estimation method treats all the peptides and proteins equally and overlooks that they could have varied probabilities of being identified. In this study, we report FineFDR, a framework for FDR assessment at fine-grained levels with taxonomy information considered. FineFDR groups the identified peptide-spectrum matches, peptides, and proteins from different taxonomic units and estimates the FDR in each group separately. Empirical experiments on the simulated and real-world data sets demonstrate that our FineFDR achieved higher precision and more peptide and protein identifications when compared to the state-of-the-art methods, such as Comet, Percolator, TIDD, and Tailor. FineFDR is freely available under the GNU GPL license at https://github.com/Biocomputing-Research-Group/FDR.</p>","PeriodicalId":74563,"journal":{"name":"Proceedings. IEEE International Conference on Bioinformatics and Biomedicine","volume":"2022 ","pages":"287-292"},"PeriodicalIF":0.0000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998077/pdf/nihms-1868490.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings. IEEE International Conference on Bioinformatics and Biomedicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/bibm55620.2022.9995401","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Microbial community proteomics, also termed metaproteomics, investigates all proteins expressed by a microbiota. Tandem mass spectrometry (MS/MS) is the typical method for identifying proteins in metaproteomics, which involves searching the mass spectra against a protein sequence database. A major post-analysis step is controlling the false discovery rate (FDR), i.e., the ratio of false positives to the total number of annotations. The current popular target-decoy FDR estimation method treats all the peptides and proteins equally and overlooks that they could have varied probabilities of being identified. In this study, we report FineFDR, a framework for FDR assessment at fine-grained levels with taxonomy information considered. FineFDR groups the identified peptide-spectrum matches, peptides, and proteins from different taxonomic units and estimates the FDR in each group separately. Empirical experiments on the simulated and real-world data sets demonstrate that our FineFDR achieved higher precision and more peptide and protein identifications when compared to the state-of-the-art methods, such as Comet, Percolator, TIDD, and Tailor. FineFDR is freely available under the GNU GPL license at https://github.com/Biocomputing-Research-Group/FDR.