Comparison of false-discovery rates of various decoy databasesopen access
- Authors
- Lee, Sangjeong; Park, Heejin; Kim, Hyunwoo
- Issue Date
- Sep-2021
- Publisher
- BMC
- Keywords
- Target-decoy search; False discovery rate; Reverse decoy database; Shuffle decoy database
- Citation
- PROTEOME SCIENCE, v.19, no.1, pp.1 - 7
- Indexed
- SCIE
SCOPUS
- Journal Title
- PROTEOME SCIENCE
- Volume
- 19
- Number
- 1
- Start Page
- 1
- End Page
- 7
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/141136
- DOI
- 10.1186/s12953-021-00179-7
- Abstract
- Background The target-decoy strategy effectively estimates the false-discovery rate (FDR) by creating a decoy database with a size identical to that of the target database. Decoy databases are created by various methods, such as, the reverse, pseudo-reverse, shuffle, pseudo-shuffle, and the de Bruijn methods. FDR is sometimes over- or under-estimated depending on which decoy database is used because the ratios of redundant peptides in the target databases are different, that is, the numbers of unique (non-redundancy) peptides in the target and decoy databases differ. Results We used two protein databases (the UniProt Saccharomyces cerevisiae protein database and the UniProt human protein database) to compare the FDRs of various decoy databases. When the ratio of redundant peptides in the target database is low, the FDR is not overestimated by any decoy construction method. However, if the ratio of redundant peptides in the target database is high, the FDR is overestimated when the (pseudo) shuffle decoy database is used. Additionally, human and S. cerevisiae six frame translation databases, which are large databases, also showed outcomes similar to that from the UniProt human protein database. Conclusion The FDR must be estimated using the correction factor proposed by Elias and Gygi or that by Kim et al. when (pseudo) shuffle decoy databases are used.
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