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Cite this article
Wittwer LD, Piližota I, Altenhoff AM, Dessimoz C.2014. Speeding up all-against-all protein comparisons while maintaining sensitivity by considering subsequence-level homology. PeerJ PrePrints2:e421v1https://doi.org/10.7287/peerj.preprints.421v1
Orthology inference and other sequence analyses across multiple genomes typically start by performing exhaustive pairwise sequence comparisons, a process referred to as “all-against-all”. As this process scales quadratically in terms of the number of sequences analysed, this step can become a bottleneck, thus limiting the number of genomes that can be simultaneously analysed. Here, we explored ways of speeding-up the all-against-all step while maintaining its sensitivity. By exploiting the transitivity of homology and, crucially, ensuring that homology is defined in terms of consistent protein subsequences, our proof-of-concept decreased the time complexity by ~75% while recovering >99.6% of all homologs identified by the full all-against-all procedure on empirical sequences from bacteria and fungi. In comparison, state-of-the-art k-mer approaches are orders of magnitude faster but only recover 3-14% of all homologous pairs. We also outline ideas to further improve the speed and recall of the new approach. An open source implementation is provided as part of the OMA standalone software at http://omabrowser.org/standalone .
This manuscript is currently undergoing peer-review at PeerJ. It is meant to be a contribution to the GNOME 2014 symposium.
List of species included in the analyses
A table containing the list of species used in the comparisons, including scientific name, taxonomic ID, primary source, and version number.
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