Evidence map›Paper›PMID 32411534›Full record

ArticlePeerJ2020

Fast sequence-based microsatellite genotyping development workflow.

Olivier Lepais, Emilie Chancerel, Christophe Boury, Franck Salin, Aurélie Manicki, Laura Taillebois, Cyril Dutech, Abdeldjalil Aissi, Cecile F E Bacles, Françoise Daverat and 2 more

Abstract read
In one paragraph

Article in PeerJ, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Article
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  9. Article
  10. Genome-Wide Microsatellites inAnimals : an open access journal from MDPI · 2024
    Article
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  12. Article
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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

12 authors.

Olivier LepaisINRAE, Univ. Bordeaux, BIOGECO, Cestas, France.
Emilie ChancerelINRAE, Univ. Bordeaux, BIOGECO, Cestas, France.
Christophe BouryINRAE, Univ. Bordeaux, BIOGECO, Cestas, France.
Franck SalinINRAE, Univ. Bordeaux, BIOGECO, Cestas, France.
Aurélie ManickiINRAE, Université de Pau et Pays de l'Adour, ECOBIOP, Saint-Peé-sur-Nivelle, France.
Laura TailleboisINRAE, Université de Pau et Pays de l'Adour, ECOBIOP, Saint-Peé-sur-Nivelle, France.
Cyril DutechINRAE, Univ. Bordeaux, BIOGECO, Cestas, France.
Abdeldjalil AissiLAPAPEZA, University of Batna 1 Hadj Lakhdar, Batna, Algeria.
Cecile F E BaclesINRAE, Université de Pau et Pays de l'Adour, ECOBIOP, Saint-Peé-sur-Nivelle, France.
Françoise DaveratINRAE, EABX, Cestas, France.
Sophie LauneyINRAE, Agrocampus Ouest, ESE, Ecology and Ecosystem Health, Rennes, France.
Erwan GuichouxINRAE, Univ. Bordeaux, BIOGECO, Cestas, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Application of high-throughput sequencing technologies to microsatellite genotyping (SSRseq) has been shown to remove many of the limitations of electrophoresis-based methods and to refine inference of population genetic diversity and structure. We present here a streamlined SSRseq development workflow that includes microsatellite development, multiplexed marker amplification and sequencing, and automated bioinformatics data analysis. We illustrate its application to five groups of species across phyla (fungi, plant, insect and fish) with different levels of genomic resource availability. We found that relying on previously developed microsatellite assay is not optimal and leads to a resulting low number of reliable locus being genotyped. In contrast, de novo ad hoc primer designs gives highly multiplexed microsatellite assays that can be sequenced to produce high quality genotypes for 20-40 loci. We highlight critical upfront development factors to consider for effective SSRseq setup in a wide range of situations. Sequence analysis accounting for all linked polymorphisms along the sequence quickly generates a powerful multi-allelic haplotype-based genotypic dataset, calling to new theoretical and analytical frameworks to extract more information from multi-nucleotide polymorphism marker systems.

Indexed as

Haplotype sequenceHapSTRSequence-based microsatellite genotypingSNPSTRSSR-GBSSSR-seq

Identifiers

PMID32411534
PMCPMC7204839

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.