Evidence map›Paper›PMID 25757407›Full record

ArticleHeredity2015

Large-scale genotyping of highly polymorphic loci by next-generation sequencing: how to overcome the challenges to reliably genotype individuals?

M Ferrandiz-Rovira, T Bigot, D Allainé, M-P Callait-Cardinal, A Cohas

Abstract read
In one paragraph

Article in Heredity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Genomic analysis of MHC-based mate choice in the monogamous California mouse.Behavioral ecology : official journal of the International Society for Behavioral Ecology
    Article
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

5 authors.

M Ferrandiz-Rovira1] Laboratoire Biométrie et Biologie Evolutive, Université de Lyon, CNRS, UMR5558, Université Lyon 1, F-69622, Villeurbanne, F-69000 Lyon, France [2] Université Lyon, VetAgro Sup Campus Vet, Marcy-L'Étoile, France.
T BigotLaboratoire Biométrie et Biologie Evolutive, Université de Lyon, CNRS, UMR5558, Université Lyon 1, F-69622, Villeurbanne, F-69000 Lyon, France.ORCID 0000000185044675
D AllainéLaboratoire Biométrie et Biologie Evolutive, Université de Lyon, CNRS, UMR5558, Université Lyon 1, F-69622, Villeurbanne, F-69000 Lyon, France.
M-P Callait-Cardinal1] Laboratoire Biométrie et Biologie Evolutive, Université de Lyon, CNRS, UMR5558, Université Lyon 1, F-69622, Villeurbanne, F-69000 Lyon, France [2] Université Lyon, VetAgro Sup Campus Vet, Marcy-L'Étoile, France.
A CohasLaboratoire Biométrie et Biologie Evolutive, Université de Lyon, CNRS, UMR5558, Université Lyon 1, F-69622, Villeurbanne, F-69000 Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studying the different roles of adaptive genes is still a challenge in evolutionary ecology and requires reliable genotyping of large numbers of individuals. Next-generation sequencing (NGS) techniques enable such large-scale sequencing, but stringent data processing is required. Here, we develop an easy to use methodology to process amplicon-based NGS data and we apply this methodology to reliably genotype four major histocompatibility complex (MHC) loci belonging to MHC class I and II of Alpine marmots (Marmota marmota). Our post-processing methodology allowed us to increase the number of retained reads. The quality of genotype assignment was further assessed using three independent validation procedures. A total of 3069 high-quality MHC genotypes were obtained at four MHC loci for 863 Alpine marmots with a genotype assignment error rate estimated as 0.21%. The proposed methodology could be applied to any genetic system and any organism, except when extensive copy-number variation occurs (that is, genes with a variable number of copies in the genotype of an individual). Our results highlight the potential of amplicon-based NGS techniques combined with adequate post-processing to obtain the large-scale highly reliable genotypes needed to understand the evolution of highly polymorphic functional genes.

Indexed as

AllelesAnimalsGenes, MHC Class IGenes, MHC Class IIGenotypeGenotyping TechniquesHigh-Throughput Nucleotide SequencingMarmotaMicrosatellite RepeatsReproducibility of ResultsSequence Analysis, DNA

Identifiers

PMID25757407
PMCPMC4815514

What OpenQuestion holds

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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.