Evidence map›Paper›PMID 26936924›Full record

ArticleGenetics2016

Needles: Toward Large-Scale Genomic Prediction with Marker-by-Environment Interaction.

Arne De Coninck, Bernard De Baets, Drosos Kourounis, Fabio Verbosio, Olaf Schenk, Steven Maenhout, Jan Fostier

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
5.4field-weighted citation impact, top 5% of its field
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

7 citing papers in PubMed, 61 citations in OpenAlex.

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  6. An innovative procedure of genome-wide association analysis fits studies on germplasm population and plant breeding.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2017
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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

7 authors at 4 institutions in 2 countries.

Arne De ConinckKERMIT, Department of Mathematical Modelling, Statistics and Bioinformatics, Ghent University, B-9000 Ghent, Belgium Bioinformatics Institute Ghent, Ghent University, B-9000 Ghent, Belgium arne.deconinck@ugent.be.
Bernard De BaetsKERMIT, Department of Mathematical Modelling, Statistics and Bioinformatics, Ghent University, B-9000 Ghent, Belgium Bioinformatics Institute Ghent, Ghent University, B-9000 Ghent, Belgium.ORCID 0000-0002-3876-620X
Drosos KourounisInstitute of Computational Science, Università della Svizzera italiana, CH-6904 Lugano, Switzerland.
Fabio VerbosioInstitute of Computational Science, Università della Svizzera italiana, CH-6904 Lugano, Switzerland.
Olaf SchenkInstitute of Computational Science, Università della Svizzera italiana, CH-6904 Lugano, Switzerland.
Steven MaenhoutProgeno, B-9052 Zwijnaarde, Belgium.
Jan FostierBioinformatics Institute Ghent, Ghent University, B-9000 Ghent, Belgium Department of Information Technology (INTEC), Ghent University-iMinds, B-9000 Ghent, Belgium.ORCID 0000-0002-9994-8269
Università della Svizzera italiana · CHGhent University · BEAblynx (Belgium) · BEiMinds · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genomic prediction relies on genotypic marker information to predict the agronomic performance of future hybrid breeds based on trial records. Because the effect of markers may vary substantially under the influence of different environmental conditions, marker-by-environment interaction effects have to be taken into account. However, this may lead to a dramatic increase in the computational resources needed for analyzing large-scale trial data. A high-performance computing solution, called Needles, is presented for handling such data sets. Needles is tailored to the particular properties of the underlying algebraic framework by exploiting a sparse matrix formalism where suited and by utilizing distributed computing techniques to enable the use of a dedicated computing cluster. It is demonstrated that large-scale analyses can be performed within reasonable time frames with this framework. Moreover, by analyzing simulated trial data, it is shown that the effects of markers with a high environmental interaction can be predicted more accurately when more records per environment are available in the training data. The availability of such data and their analysis with Needles also may lead to the discovery of highly contributing QTL in specific environmental conditions. Such a framework thus opens the path for plant breeders to select crops based on these QTL, resulting in hybrid lines with optimized agronomic performance in specific environmental conditions.

Indexed as

Gene-Environment InteractionGenome, PlantSoftwareGenetic MarkersPlant BreedingQuantitative Trait LociGenetic Markersgenomic predictiongenomic selectionGenPredhigh-performance computingmarker-by-environment interactionshared data resourcesimulated datavariance component estimation

Identifiers

PMID26936924
PMCPMC4858798
OpenAlexW2314709240

What OpenQuestion holds

Textmetadata
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.