Evidence map›Paper›PMID 27535823›Full record

ArticleBMC medical genomics2016

Fast comparison of genomic and meta-genomic reads with alignment-free measures based on quality values.

Matteo Comin, Michele Schimd

Abstract readComparative Study
In one paragraph

Article in BMC medical genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

3 citing papers in PubMed.

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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.

Matteo CominDepartment of Information Engineering, University of Padova, Via Gradenigo 6/A, Padova, Italy. comin@dei.unipd.it.
Michele SchimdDepartment of Information Engineering, University of Padova, Via Gradenigo 6/A, Padova, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSequencing technologies are generating enormous amounts of read data, however assembly of genomes and metagenomes remain among the most challenging tasks. In this paper we study the comparison of genomes and metagenomes only based on read data, using word counts statistics called alignment-free thus not requiring reference genomes or assemblies. Quality scores produced by sequencing platforms are fundamental for various analyses, moreover future-generation sequencing platforms, will produce longer reads but with error rate around 15 %. In this context it will be fundamental to exploit quality values information within the framework of alignment-free measures.

resultsIn this paper we present a family of alignment-free measures, called d (q) -type, that are based on k-mer counts and quality values. These statistics can be used to compare genomes and metagenomes based on their read sets. Results show that the evolutionary relationship of genomes can be reconstructed based on the direct comparison of theirs reads sets.

conclusionThe use of quality values on average improves the classification accuracy, and its contribution increases when the reads are more noisy. Also the comparison of metagenomic microbial communities can be performed efficiently. Similar metagenomes are quickly detected, just by processing their read data, without the need of costly alignments.

Indexed as

Evolution, MolecularMetagenomicsSequence AnalysisSoftwareAlignment-free measuresMeta-genomesPhylogeny without assemblyReads quality values

Identifiers

PMID27535823
PMCPMC4989896

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Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.