Evidence map›Paper›PMID 28606054›Full record

ArticleBMC bioinformatics2017

Variable-order sequence modeling improves bacterial strain discrimination for Ion Torrent DNA reads.

Thomas M Poulsen, Martin Frith

Abstract read
In one paragraph

Article in BMC bioinformatics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Thomas M PoulsenArtificial Intelligence Research Center, National Institute of Advanced Industrial Science and Technology (AIST), 2-3-26 Aomi, Koto-ku, Tokyo, 135-0064, Japan. thomasaistjp@gmail.com.
Martin FrithArtificial Intelligence Research Center, National Institute of Advanced Industrial Science and Technology (AIST), 2-3-26 Aomi, Koto-ku, Tokyo, 135-0064, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGenome sequencing provides a powerful tool for pathogen detection and can help resolve outbreaks that pose public safety and health risks. Mapping of DNA reads to genomes plays a fundamental role in this approach, where accurate alignment and classification of sequencing data is crucial. Standard mapping methods crudely treat bases as independent from their neighbors. Accuracy might be improved by using higher order paired hidden Markov models (HMMs), which model neighbor effects, but introduce design and implementation issues that have typically made them impractical for read mapping applications. We present a variable-order paired HMM that we term VarHMM, which addresses central issues involved with higher order modeling for sequence alignment.

resultsCompared with existing alignment methods, VarHMM is able to model higher order distributions and quantify alignment probabilities with greater detail and accuracy. In a series of comparison tests, in which Ion Torrent sequenced DNA was mapped to similar bacterial strains, VarHMM consistently provided better strain discrimination than any of the other alignment methods that we compared with.

conclusionsOur results demonstrate the advantages of higher ordered probability distribution modeling and also suggest that further development of such models would benefit read mapping in a range of other applications as well.

Indexed as

DNA, BacterialGenome, BacterialGenomicsMarkov ChainsSequence AlignmentSequence Analysis, DNADNA, BacterialHigher orderHMMIon TorrentPathogen detectionSequence alignment

Identifiers

PMID28606054
PMCPMC5469136

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LicenceCC BY
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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.