Evidence map›Paper›PMID 29040374›Full record

ArticleBioinformatics (Oxford, England)2018

Beyond similarity assessment: selecting the optimal model for sequence alignment via the Factorized Asymptotic Bayesian algorithm.

Taikai Takeda, Michiaki Hamada, John Hancock

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Taikai TakedaDepartment of Electrical Engineering and Bioscience, Faculty of Science and Engineering, Waseda University, Tokyo 169-8555, Japan.
Michiaki HamadaDepartment of Electrical Engineering and Bioscience, Faculty of Science and Engineering, Waseda University, Tokyo 169-8555, Japan.
John Hancock

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: Pair Hidden Markov Models (PHMMs) are probabilistic models used for pairwise sequence alignment, a quintessential problem in bioinformatics. PHMMs include three types of hidden states: match, insertion and deletion. Most previous studies have used one or two hidden states for each PHMM state type. However, few studies have examined the number of states suitable for representing sequence data or improving alignment accuracy. Results: We developed a novel method to select superior models (including the number of hidden states) for PHMM. Our method selects models with the highest posterior probability using Factorized Information Criterion, which is widely utilized in model selection for probabilistic models with hidden variables. Our simulations indicated that this method has excellent model selection capabilities with slightly improved alignment accuracy. We applied our method to DNA datasets from 5 and 28 species, ultimately selecting more complex models than those used in previous studies. Availability and implementation: The software is available at https://github.com/bigsea-t/fab-phmm. Contact: mhamada@waseda.jp. Supplementary information: Supplementary data are available at Bioinformatics online.

Indexed as

SoftwareAlgorithmsAnimalsBayes TheoremComputational BiologyHumansModels, StatisticalSequence AlignmentSequence Analysis, DNASequence Analysis, ProteinSequence Analysis, RNA

Identifiers

PMID29040374
PMCPMC5860613

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.