Evidence map›Paper›PMID 30382832›Full record

ArticleBMC bioinformatics2018

A fully automated pipeline for quantitative genotype calling from next generation sequencing data in autopolyploids.

Guilherme S Pereira, Antonio Augusto F Garcia, Gabriel R A Margarido

Abstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
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  4. Genomic prediction with allele dosage information in highly polyploid species.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2022
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
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  11. Construction of a High-Density Genetic Map ofFrontiers in plant science · 2021
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Genotype calling of triploid offspring from diploid parents.Genetics, selection, evolution : GSE · 2020
    Article
  18. Article
  19. Article
  20. Development of an Axiom Sugarcane100K SNP array for genetic map construction and QTL identification.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2019
    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

3 authors.

Guilherme S PereiraUniversity of São Paulo, "Luiz de Queiroz" College of Agriculture, Department of Genetics, Av Pádua Dias, 11, Piracicaba, 13400-970, Brazil.
Antonio Augusto F GarciaUniversity of São Paulo, "Luiz de Queiroz" College of Agriculture, Department of Genetics, Av Pádua Dias, 11, Piracicaba, 13400-970, Brazil.
Gabriel R A MargaridoUniversity of São Paulo, "Luiz de Queiroz" College of Agriculture, Department of Genetics, Av Pádua Dias, 11, Piracicaba, 13400-970, Brazil. gramarga@usp.br.ORCID http://orcid.org/0000-0002-2327-0201

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 312448/2013-9Fundação de Amparo à Pesquisa do Estado de São Paulo #2008/52197-4Fundação de Amparo à Pesquisa do Estado de São Paulo #2012/25236-4Fundação de Amparo à Pesquisa do Estado de São Paulo #2015/22993-7
6 · The paper itself

Abstract

backgroundGenotyping-by-sequencing (GBS) has been used broadly in genetic studies for several species, especially those with agricultural importance. However, its use is still limited in autopolyploid species because genotype calling software generally fails to properly distinguish heterozygous classes based on allele dosage.

resultsVCF2SM is a Python script that integrates sequencing depth information of polymorphisms in variant call format (VCF) files and SUPERMASSA software for quantitative genotype calling. VCFs can be obtained from any variant discovery software that outputs exact allele sequencing depth, such as a modified version of the TASSEL-GBS pipeline provided here. VCF2SM was successfully applied in analyzing GBS data from diverse panels (alfalfa and potato) and full-sib mapping populations (alfalfa and switchgrass) of polyploid species.

conclusionsWe demonstrate that our approach can help plant geneticists working with autopolyploid species to advance their studies by distinguishing allele dosage from GBS data.

Indexed as

Polymorphism, Single NucleotidePolyploidySoftwareAutomation, LaboratoryGenetic MarkersGenotypeGenotyping TechniquesHigh-Throughput Nucleotide SequencingMedicago sativaSolanum tuberosumGenetic MarkersAllele dosageGenotyping-by-sequencingGWASLinkage mappingPloidy estimationPopulation structure

Identifiers

PMID30382832
PMCPMC6211426

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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.