A BLAST from the past: revisiting blastp's E-value

Bioinformatics. 2024 Nov 28;40(12):btae729. doi: 10.1093/bioinformatics/btae729.

Abstract

Motivation: The Basic Local Alignment Search Tool, BLAST, is an indispensable tool for genomic research. BLAST has established itself as the canonical tool for sequence similarity search in large part thanks to its meaningful statistical analysis. Specifically, BLAST reports the E-value of each reported alignment, which is defined as the expected number of optimal local alignments that will score at least as high as the observed alignment score, assuming that the query and the database sequences are randomly generated.

Results: Here, we critically evaluate the E-values provided by the standard protein BLAST (blastp), showing that they can be at times significantly conservative while at others too liberal. We offer an alternative approach based on generating a small sample from the null distribution of random optimal alignments, and testing whether the observed alignment score is consistent with it. In contrast with blastp, our significance analysis seems valid, in the sense that it did not deliver inflated significance estimates in any of our extensive experiments. Moreover, although our method is slightly conservative, it is often significantly less so than the blastp E-value. Indeed, in cases where blastp's analysis is valid (i.e., not too liberal), our approach seems to deliver a greater number of correct alignments. One advantage of our approach is that it works with any reasonable choice of substitution matrix and gap penalties, avoiding blastp's limited options of matrices and penalties. In addition, we can formulate the problem using a canonical family-wise error rate control setup, thereby dispensing with E-values, which can at times be difficult to interpret.

Availability and implementation: The Apache licensed source code is available at https://github.com/batmen-lab/SGPvalue.

MeSH terms

  • Algorithms
  • Computational Biology / methods
  • Databases, Protein
  • Genomics / methods
  • Proteins / chemistry
  • Sequence Alignment* / methods
  • Sequence Analysis, Protein / methods
  • Software

Substances

  • Proteins