Abstract

Automated database search engines are one of the fundamental engines of high-throughput proteomics enabling daily identifications of hundreds of thousands of peptides and proteins from tandem mass (MS/MS) spectrometry data. Nevertheless, this automation also makes it humanly impossible to manually validate the vast lists of resulting identifications from such high-throughput searches. This challenge is usually addressed by using a Target-Decoy Approach (TDA) to impose an empirical False Discovery Rate (FDR) at a pre-determined threshold x% with the expectation that at most x% of the returned identifications would be false positives. But despite the fundamental importance of FDR estimates in ensuring the utility of large lists of identifications, there is surprisingly little consensus on exactly how TDA should be applied to minimize the chances of biased FDR estimates. In fact, since less rigorous TDA/FDR estimates tend to result in more identifications (at higher 'true' FDR), there is often little incentive to enforce strict TDA/FDR procedures in studies where the major metric of success is the size of the list of identifications and there are no follow up studies imposing hard cost constraints on the number of reported false positives.Here we address the problem of the accuracy of TDA estimates of empirical FDR. Using MS/MS spectra from samples where we were able to define a factual FDR estimator of 'true' FDR we evaluate several popular variants of the TDA procedure in a variety of database search contexts. We show that the fraction of false identifications can sometimes be over 10× higher than reported and may be unavoidably high for certain types of searches. In addition, we further report that the two-pass search strategy seems the most promising database search strategy.While unavoidably constrained by the particulars of any specific evaluation dataset, our observations support a series of recommendations towards maximizing the number of resulting identifications while controlling database searches with robust and reproducible TDA estimation of empirical FDR.

Highlights

  • Mass spectrometry (MS) based proteomics studies often generate millions of tandem mass spectra

  • To avoid biased False Discovery Rate (FDR) estimates, it is important for decoy peptide-spectrum matches (PSMs) to have a score distribution similar to that of false target PSMs

  • In contrast with popular belief, we did not observe a conservative estimation of FDR with shuffled decoy when compared to the reverse decoy database. 1the empirical FDR; 2the factual FDR; 3 the number of positive target PSMs; 4 Fisher p-value - Fisher p-values less than 5% were emphasized with bold fonts

Read more

Summary

Introduction

Mass spectrometry (MS) based proteomics studies often generate millions of tandem mass spectra. There are numerous database search engines available such as SEQUEST [1], Mascot [2], X!Tandem [3], OMSSA [4], InsPecT [5] and MS-GFDB [6]. These engines take a set of spectra and a protein database as the input and output peptide-spectrum matches (PSMs) by scoring each spectrum against the peptides in the database and assigning the best-scoring peptide as a “match” to each spectrum.

Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call