Prediction of missing sequences and branch lengths in phylogenomic data.
basic_science · Level V
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- Record sourced from PubMed, PMID 26733454.
- Also identified by DOI 10.1093/bioinformatics/btv768.
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Abstract
The presence of missing data in large-scale phylogenomic datasets has negative effects on the phylogenetic inference process. One effect that is caused by alignments with missing per-gene or per-partition sequences is that the inferred phylogenies may exhibit extremely long branch lengths. We investigate if statistically predicting missing sequences for organisms by using information from genes/partitions that have data for these organisms alleviates the problem and improves phylogenetic accuracy. We present several algorithms for correcting excessively long branch lengths induced by missing data. We also present methods for predicting/imputing missing sequence data. We evaluate our algorithms by systematically removing sequence data from three empirical and 100 simulated alignments. We then compare the Maximum Likelihood trees inferred from the gappy alignments and on the alignments with predicted sequence data to the trees inferred from the original, complete datasets. The datasets with predicted sequences showed one to two orders of magnitude more accurate branch lengths compared to the branch lengths of the trees inferred from the alignments with missing data. However, prediction did not affect the RF distances between the trees. https://github.com/ddarriba/ForeSeqs : diego.darriba@h-its.org Supplementary data are available at Bioinformatics online.
Medical subject headings
- Phylogeny
- Sequence Alignment