Evidence map›Paper›PMID 23216988›Full record

ArticleBMC bioinformatics2012

Improving stability and understandability of genotype-phenotype mapping in Saccharomyces using regularized variable selection in L-PLS regression.

Tahir Mehmood, Jonas Warringer, Lars Snipen, Solve Sæbø

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2012. 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
0.6field-weighted citation impact, top 26% 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, 13 citations in OpenAlex.

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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 at 2 institutions in 2 countries.

Tahir MehmoodBiostatistics, Department of Chemistry, Biotechnology and Food Sciences, Norwegian University of Life Sciences, Ås, Norway. tahir.mehmood@umb.no
Jonas Warringer
Lars Snipen
Solve Sæbø
Norwegian University of Life Sciences · NOUniversity of Gothenburg · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultivariate approaches have been successfully applied to genome wide association studies. Recently, a Partial Least Squares (PLS) based approach was introduced for mapping yeast genotype-phenotype relations, where background information such as gene function classification, gene dispensability, recent or ancient gene copy number variations and the presence of premature stop codons or frameshift mutations in reading frames, were used post hoc to explain selected genes. One of the latest advancement in PLS named L-Partial Least Squares (L-PLS), where 'L' presents the used data structure, enables the use of background information at the modeling level. Here, a modification of L-PLS with variable importance on projection (VIP) was implemented using a stepwise regularized procedure for gene and background information selection. Results were compared to PLS-based procedures, where no background information was used.

resultsApplying the proposed methodology to yeast Saccharomyces cerevisiae data, we found the relationship between genotype-phenotype to have improved understandability. Phenotypic variations were explained by the variations of relatively stable genes and stable background variations. The suggested procedure provides an automatic way for genotype-phenotype mapping. The selected phenotype influencing genes were evolving 29% faster than non-influential genes, and the current results are supported by a recently conducted study. Further power analysis on simulated data verified that the proposed methodology selects relevant variables.

conclusionsA modification of L-PLS with VIP in a stepwise regularized elimination procedure can improve the understandability and stability of selected genes and background information. The approach is recommended for genome wide association studies where background information is available.

Indexed as

GenotypePhenotypeGenetic Association StudiesLeast-Squares AnalysisSaccharomyces cerevisiae

Identifiers

PMID23216988
PMCPMC3598729
OpenAlexW2169764104

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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.