Evidence map›Paper›PMID 24516366›Full record

ArticleTheScientificWorldJournal2014

Large scale explorative oligonucleotide probe selection for thousands of genetic groups on a computing grid: application to phylogenetic probe design using a curated small subunit ribosomal RNA gene database.

Faouzi Jaziri, Eric Peyretaillade, Mohieddine Missaoui, Nicolas Parisot, Sébastien Cipière, Jérémie Denonfoux, Antoine Mahul, Pierre Peyret, David R C Hill

Abstract read
In one paragraph

Article in TheScientificWorldJournal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Faouzi JaziriUMR CNRS 6158, ISIMA/LIMOS, Clermont Université et Université Blaise Pascal, F63173 Aubière, France ; Clermont Université et Université d'Auvergne, EA 4678 CIDAM, BP 10448, F63001 Clermont-Ferrand Cedex 1, France.
Eric PeyretailladeClermont Université et Université d'Auvergne, EA 4678 CIDAM, BP 10448, F63001 Clermont-Ferrand Cedex 1, France ; Clermont Université et Université d'Auvergne, UFR Pharmacie, F63001 Clermont-Ferrand Cedex 1, France.
Mohieddine MissaouiUMR CNRS 6158, ISIMA/LIMOS, Clermont Université et Université Blaise Pascal, F63173 Aubière, France ; Clermont Université et Université d'Auvergne, EA 4678 CIDAM, BP 10448, F63001 Clermont-Ferrand Cedex 1, France.
Nicolas ParisotClermont Université et Université d'Auvergne, EA 4678 CIDAM, BP 10448, F63001 Clermont-Ferrand Cedex 1, France ; CNRS, UMR 6023, LMGE, F63171 Aubière, France.
Sébastien CipièreUMR CNRS 6158, ISIMA/LIMOS, Clermont Université et Université Blaise Pascal, F63173 Aubière, France.
Jérémie DenonfouxClermont Université et Université d'Auvergne, EA 4678 CIDAM, BP 10448, F63001 Clermont-Ferrand Cedex 1, France ; CNRS, UMR 6023, LMGE, F63171 Aubière, France.
Antoine MahulClermont Université, CRRI, F63177 Aubière, France.
Pierre PeyretClermont Université et Université d'Auvergne, EA 4678 CIDAM, BP 10448, F63001 Clermont-Ferrand Cedex 1, France ; Clermont Université et Université d'Auvergne, UFR Pharmacie, F63001 Clermont-Ferrand Cedex 1, France.
David R C HillUMR CNRS 6158, ISIMA/LIMOS, Clermont Université et Université Blaise Pascal, F63173 Aubière, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phylogenetic Oligonucleotide Arrays (POAs) were recently adapted for studying the huge microbial communities in a flexible and easy-to-use way. POA coupled with the use of explorative probes to detect the unknown part is now one of the most powerful approaches for a better understanding of microbial community functioning. However, the selection of probes remains a very difficult task. The rapid growth of environmental databases has led to an exponential increase of data to be managed for an efficient design. Consequently, the use of high performance computing facilities is mandatory. In this paper, we present an efficient parallelization method to select known and explorative oligonucleotide probes at large scale using computing grids. We implemented a software that generates and monitors thousands of jobs over the European Computing Grid Infrastructure (EGI). We also developed a new algorithm for the construction of a high-quality curated phylogenetic database to avoid erroneous design due to bad sequence affiliation. We present here the performance and statistics of our method on real biological datasets based on a phylogenetic prokaryotic database at the genus level and a complete design of about 20,000 probes for 2,069 genera of prokaryotes.

Indexed as

Oligonucleotide ProbesSoftwareAlgorithmsComputational BiologyDatabases, Nucleic AcidGenes, rRNAOligonucleotide Array Sequence AnalysisPhylogenyOligonucleotide Probes

Identifiers

PMID24516366
PMCPMC3913353

What OpenQuestion holds

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LicenceCC BY
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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.