Evidence map›Paper›PMID 33344093›Full record

ArticleApplications in plant sciences2020

SSRgenotyper: A simple sequence repeat genotyping application for whole-genome resequencing and reduced representational sequencing projects.

Daniel H Lewis, David E Jarvis, Peter J Maughan

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Article in Applications in plant sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Daniel H LewisDepartment of Plant and Wildlife Sciences Brigham Young University Provo Utah 84058 USA.
David E JarvisDepartment of Plant and Wildlife Sciences Brigham Young University Provo Utah 84058 USA.ORCID https://orcid.org/0000-0002-0072-9112
Peter J MaughanDepartment of Plant and Wildlife Sciences Brigham Young University Provo Utah 84058 USA.ORCID https://orcid.org/0000-0003-3714-3411

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

premiseMany programs can identify simple sequence repeat (SSR) motifs in genomic data. SSRgenotyper extends SSR identification to en masse genotyping from resequencing data for diversity panels and linkage mapping populations. METHODS AND

resultsSSRgenotyper will find and genotype SSRs from SAM files and an SSR reference FASTA. Several outputs are possible, including a simple table with the SSR marker name, position, and SSR alleles, defined by the repeat number of the repeat motif. Specific output files include a GENEPOP-formatted file for downstream genetic diversity analyses and a traditional A, H, B mapping file output that is phased to the parents of the population for biparental linkage map construction. Linkage maps produced using SSRgenotyper genotypes were highly collinear with physical maps and correctly inferred known phylogenies.

conclusionsSSRgenotyper provides an easy-to-use, accurate, and scalable SSR genotyping platform for whole-genome resequencing data. SSRgenotyper is freely available at https://github.com/dlewis27/SSRgenotyper.

Indexed as

genotypinglinkage mappingmicrosatellitesimple sequence repeatsimple tandem repeat

Identifiers

PMID33344093
PMCPMC7742204

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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.