Evidence map›Paper›PMID 24845653›Full record

ArticleBioinformatics (Oxford, England)2014

Exploration and retrieval of whole-metagenome sequencing samples.

Sohan Seth, Niko Välimäki, Samuel Kaski, Antti Honkela

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

13 citing papers in PubMed.

  1. Current Status of Next-Generation Sequencing in Bone Genetic Diseases.International journal of molecular sciences · 2023
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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

4 authors.

Sohan SethHelsinki Institute for Information Technology HIIT, Department of Information and Computer Science, Aalto University, Espoo, Finland, Genome-Scale Biology Program and Department of Medical Genetics, University of Helsinki, Helsinki, Finland, and Helsinki Institute for Information Technology HIIT, Department of Computer Science, University of Helsinki, Helsinki, Finland.
Niko VälimäkiHelsinki Institute for Information Technology HIIT, Department of Information and Computer Science, Aalto University, Espoo, Finland, Genome-Scale Biology Program and Department of Medical Genetics, University of Helsinki, Helsinki, Finland, and Helsinki Institute for Information Technology HIIT, Department of Computer Science, University of Helsinki, Helsinki, Finland Helsinki Institute for Information Technology HIIT, Department of Information and Computer Science, Aalto University, Espoo, Finland, Genome-Scale Biology Program and Department of Medical Genetics, University of Helsinki, Helsinki, Finland, and Helsinki Institute for Information Technology HIIT, Department of Computer Science, University of Helsinki, Helsinki, Finland.
Samuel KaskiHelsinki Institute for Information Technology HIIT, Department of Information and Computer Science, Aalto University, Espoo, Finland, Genome-Scale Biology Program and Department of Medical Genetics, University of Helsinki, Helsinki, Finland, and Helsinki Institute for Information Technology HIIT, Department of Computer Science, University of Helsinki, Helsinki, Finland Helsinki Institute for Information Technology HIIT, Department of Information and Computer Science, Aalto University, Espoo, Finland, Genome-Scale Biology Program and Department of Medical Genetics, University of Helsinki, Helsinki, Finland, and Helsinki Institute for Information Technology HIIT, Department of Computer Science, University of Helsinki, Helsinki, Finland.
Antti HonkelaHelsinki Institute for Information Technology HIIT, Department of Information and Computer Science, Aalto University, Espoo, Finland, Genome-Scale Biology Program and Department of Medical Genetics, University of Helsinki, Helsinki, Finland, and Helsinki Institute for Information Technology HIIT, Department of Computer Science, University of Helsinki, Helsinki, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationOver the recent years, the field of whole-metagenome shotgun sequencing has witnessed significant growth owing to the high-throughput sequencing technologies that allow sequencing genomic samples cheaper, faster and with better coverage than before. This technical advancement has initiated the trend of sequencing multiple samples in different conditions or environments to explore the similarities and dissimilarities of the microbial communities. Examples include the human microbiome project and various studies of the human intestinal tract. With the availability of ever larger databases of such measurements, finding samples similar to a given query sample is becoming a central operation.

resultsIn this article, we develop a content-based exploration and retrieval method for whole-metagenome sequencing samples. We apply a distributed string mining framework to efficiently extract all informative sequence k-mers from a pool of metagenomic samples and use them to measure the dissimilarity between two samples. We evaluate the performance of the proposed approach on two human gut metagenome datasets as well as human microbiome project metagenomic samples. We observe significant enrichment for diseased gut samples in results of queries with another diseased sample and high accuracy in discriminating between different body sites even though the method is unsupervised. AVAILABILITY AND IMPLEMENTATION: A software implementation of the DSM framework is available at https://github.com/HIITMetagenomics/dsm-framework. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

AlgorithmsData MiningDiabetes Mellitus, Type 2High-Throughput Nucleotide SequencingHumansInflammatory Bowel DiseasesMetagenomicsMicrobiotaSequence Analysis, DNA

Identifiers

PMID24845653
PMCPMC4230234

What OpenQuestion holds

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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.