Evidence map›Paper›PMID 30541448›Full record

ArticleBMC genomics2018

Accuracy of RNAseq based SNP discovery and genotyping in Populusnigra.

Odile Rogier, Aurélien Chateigner, Souhila Amanzougarene, Marie-Claude Lesage-Descauses, Sandrine Balzergue, Véronique Brunaud, José Caius, Ludivine Soubigou-Taconnat, Véronique Jorge, Vincent Segura

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 41 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

10 authors at 3 institutions in 2 countries.

Odile RogierBioForA, INRA, ONF, Orléans, 45075, France.
Aurélien ChateignerBioForA, INRA, ONF, Orléans, 45075, France.
Souhila AmanzougareneBioForA, INRA, ONF, Orléans, 45075, France.
Marie-Claude Lesage-DescausesBioForA, INRA, ONF, Orléans, 45075, France.
Sandrine BalzergueInstitute of Plant Sciences Paris-Saclay (IPS2), CNRS, INRA, Université Paris-Sud, Université Paris-Saclay, Université d'Evry, Université Paris-Diderot, Sorbonne Paris-Cité, Orsay, 91405, France.
Véronique BrunaudInstitute of Plant Sciences Paris-Saclay (IPS2), CNRS, INRA, Université Paris-Sud, Université Paris-Saclay, Université d'Evry, Université Paris-Diderot, Sorbonne Paris-Cité, Orsay, 91405, France.
José CaiusInstitute of Plant Sciences Paris-Saclay (IPS2), CNRS, INRA, Université Paris-Sud, Université Paris-Saclay, Université d'Evry, Université Paris-Diderot, Sorbonne Paris-Cité, Orsay, 91405, France.
Ludivine Soubigou-TaconnatInstitute of Plant Sciences Paris-Saclay (IPS2), CNRS, INRA, Université Paris-Sud, Université Paris-Saclay, Université d'Evry, Université Paris-Diderot, Sorbonne Paris-Cité, Orsay, 91405, France.
Véronique JorgeBioForA, INRA, ONF, Orléans, 45075, France.
Vincent SeguraBioForA, INRA, ONF, Orléans, 45075, France. vincent.segura@inra.fr.ORCID http://orcid.org/0000-0003-1860-2256
Université d'Orléans · FRUniversité Paris-Sud · FRInstitut National de la Recherche Agronomique · MA

Funding

Agence Nationale de la Recherche ANR-10-LABX-0040-SPSAgence Nationale de la Recherche ANR-13-JSV6-0001
6 · The paper itself

Abstract

backgroudPopulus nigra is a major tree species of ecological and economic importance for which several initiatives have been set up to create genomic resources. In order to access the large number of Single Nucleotide Polymorphisms (SNPs) typically needed to carry out a genome scan, the present study aimed at evaluating RNA sequencing as a tool to discover and type SNPs in genes within natural populations of P. nigra.

resultsWe have devised a bioinformatics pipeline to call and type SNPs from RNAseq reads and applied it to P. nigra transcriptomic data. The accuracy of the resulting RNAseq-based SNP calling and typing has been evaluated by (i) comparing their position and alleles to those previously reported in candidate genes, (ii) assessing their genotyping accuracy with respect to a previously available SNP chip and (iii) evaluating their inter-annual repeatability. We found that a combination of several callers yields a good compromise between the number of variants type and the accuracy of genotyping. We further used the resulting genotypic data to carry out basic genetic analyses whose results confirm the quality of the RNAseq-based SNP dataset.

conclusionsWe demonstrated the potential and accuracy of RNAseq as an efficient way to genotype SNPs in P. nigra. These results open prospects towards the use of this technology for quantitative and population genomics studies.

Indexed as

Genes, PlantPolymorphism, Single Nucleotide3' Untranslated Regions5' Untranslated RegionsChromosome MappingCluster AnalysisExonsGenotypeHigh-Throughput Nucleotide SequencingPopulusRNA, PlantSequence Analysis, RNA3' Untranslated Regions5' Untranslated RegionsRNA, PlantBioinformatics pipelineBlack poplarDNA polymorphismsTranscriptomics

Identifiers

PMID30541448
PMCPMC6291945
OpenAlexW2905161160

What OpenQuestion holds

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.