UPP2: fast and accurate alignment of datasets with fragmentary sequences

Author:

Park Minhyuk1ORCID,Ivanovic Stefan1,Chu Gillian1,Shen Chengze1ORCID,Warnow Tandy1ORCID

Affiliation:

1. Department of Computer Science, University of Illinois Urbana-Champaign , Urbana, IL 61820, USA

Abstract

Abstract Motivation Multiple sequence alignment (MSA) is a basic step in many bioinformatics pipelines. However, achieving highly accurate alignments on large datasets, especially those with sequence length heterogeneity, is a challenging task. Ultra-large multiple sequence alignment using Phylogeny-aware Profiles (UPP) is a method for MSA estimation that builds an ensemble of Hidden Markov Models (eHMM) to represent an estimated alignment on the full-length sequences in the input, and then adds the remaining sequences into the alignment using selected HMMs in the ensemble. Although UPP provides good accuracy, it is computationally intensive on large datasets. Results We present UPP2, a direct improvement on UPP. The main advance is a fast technique for selecting HMMs in the ensemble that allows us to achieve the same accuracy as UPP but with greatly reduced runtime. We show that UPP2 produces more accurate alignments compared to leading MSA methods on datasets exhibiting substantial sequence length heterogeneity and is among the most accurate otherwise. Availability and implementation https://github.com/gillichu/sepp. Supplementary information Supplementary data are available at Bioinformatics online.

Funder

National Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

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