Evidence map›Paper›PMID 34152681›Full record

ArticleMolecular ecology resources2022

A robust sequencing assay of a thousand amplicons for the high-throughput population monitoring of Alpine ibex immunogenetics.

Camille Kessler, Alice Brambilla, Dominique Waldvogel, Glauco Camenisch, Iris Biebach, Deborah M Leigh, Christine Grossen, Daniel Croll

Open access · hybridAbstract read
In one paragraph

Article in Molecular ecology resources, 2022. 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
0.9field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 10 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

8 authors at 2 institutions in 2 countries.

Camille KesslerLaboratory of Evolutionary Genetics, Institute of Biology, University of Neuchâtel, Neuchâtel, Switzerland.
Alice BrambillaDepartment of Evolutionary Biology and Environmental Studies, University of Zürich, Zürich, Switzerland.
Dominique WaldvogelDepartment of Evolutionary Biology and Environmental Studies, University of Zürich, Zürich, Switzerland.
Glauco CamenischDepartment of Evolutionary Biology and Environmental Studies, University of Zürich, Zürich, Switzerland.
Iris BiebachDepartment of Evolutionary Biology and Environmental Studies, University of Zürich, Zürich, Switzerland.
Deborah M LeighDepartment of Evolutionary Biology and Environmental Studies, University of Zürich, Zürich, Switzerland.ORCID https://orcid.org/0000-0003-3902-2568
Christine GrossenDepartment of Evolutionary Biology and Environmental Studies, University of Zürich, Zürich, Switzerland.
Daniel CrollLaboratory of Evolutionary Genetics, Institute of Biology, University of Neuchâtel, Neuchâtel, Switzerland.ORCID https://orcid.org/0000-0002-2072-380X
University of Zurich · CHUniversity of Neuchâtel · CH

Funding

Interreg Alcotra LEMED-IBEXSchweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 198147
6 · The paper itself

Abstract

Polymorphism for immune functions can explain significant variation in health and reproductive success within species. Drastic loss in genetic diversity at such loci constitutes an extinction risk and should be monitored in species of conservation concern. However, effective implementations of genome-wide immune polymorphism sets into high-throughput genotyping assays are scarce. Here, we report the design and validation of a microfluidics-based amplicon sequencing assay to comprehensively capture genetic variation in Alpine ibex (Capra ibex). This species represents one of the most successful large mammal restorations recovering from a severely depressed census size and a massive loss in diversity at the major histocompatibility complex (MHC). We analysed 65 whole-genome sequencing sets of the Alpine ibex and related species to select the most representative markers and to prevent primer binding failures. In total, we designed ~1,000 amplicons densely covering the MHC, further immunity-related genes as well as randomly selected genome-wide markers for the assessment of neutral population structure. Our analysis of 158 individuals shows that the genome-wide markers perform equally well at resolving population structure as RAD-sequencing or low-coverage genome sequencing data sets. Immunity-related loci show unexpectedly high degrees of genetic differentiation within the species. Such information can now be used to define highly targeted individual translocations. Our design strategy can be realistically implemented into genetic surveys of a large range of species. In conclusion, leveraging whole-genome sequencing data sets to design targeted amplicon assays allows the simultaneous monitoring of multiple genetic risk factors and can be translated into species conservation recommendations.

Indexed as

GoatsImmunogeneticsAnimalsHumansadaptationconservation geneticsgenomics/proteomicspopulation genetics - empiricalwildlife management

Identifiers

PMID34152681
PMCPMC9292246
OpenAlexW3175394907

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.