Evidence map›Paper›PMID 26305794›Full record

ArticlePloS one2015

Genomic Variants Revealed by Invariably Missing Genotypes in Nelore Cattle.

Joaquim Manoel da Silva, Poliana Fernanda Giachetto, Luiz Otávio Campos da Silva, Leandro Carrijo Cintra, Samuel Rezende Paiva, Alexandre Rodrigues Caetano, Michel Eduardo Beleza Yamagishi

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Joaquim Manoel da SilvaFaculdade de Ciências Agrárias, Biológicas e Sociais Aplicadas, Universidade do Estado de Mato Grosso (UNEMAT), Nova Xavantina, Mato Grosso, Brazil; Programa de Pós-Graduação em Genética e Biologia Molecular-Instituto de Biologia, Universidade Estadual de Campinas (UNICAMP), Campinas, São Paulo, Brazil.
Poliana Fernanda GiachettoLaboratório Multiusuário de Bioinformática (LMB)-Embrapa Informática Agropecuária, Campinas, São Paulo, Brazil.
Luiz Otávio Campos da SilvaEmbrapa Gado de Corte, Campo Grande, Mato Grosso do Sul, Brazil.
Leandro Carrijo CintraLaboratório Multiusuário de Bioinformática (LMB)-Embrapa Informática Agropecuária, Campinas, São Paulo, Brazil.
Samuel Rezende PaivaEmbrapa-Secretaria de Relações Internacionais, Brasília, Distrito Federal, Brazil.
Alexandre Rodrigues CaetanoEmbrapa Recursos Genéticos e Biotecnologia, Brasília, Distrito Federal, Brazil.
Michel Eduardo Beleza YamagishiLaboratório Multiusuário de Bioinformática (LMB)-Embrapa Informática Agropecuária, Campinas, São Paulo, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High density genotyping panels have been used in a wide range of applications. From population genetics to genome-wide association studies, this technology still offers the lowest cost and the most consistent solution for generating SNP data. However, in spite of the application, part of the generated data is always discarded from final datasets based on quality control criteria used to remove unreliable markers. Some discarded data consists of markers that failed to generate genotypes, labeled as missing genotypes. A subset of missing genotypes that occur in the whole population under study may be caused by technical issues but can also be explained by the presence of genomic variations that are in the vicinity of the assayed SNP and that prevent genotyping probes from annealing. The latter case may contain relevant information because these missing genotypes might be used to identify population-specific genomic variants. In order to assess which case is more prevalent, we used Illumina HD Bovine chip genotypes from 1,709 Nelore (Bos indicus) samples. We found 3,200 missing genotypes among the whole population. NGS re-sequencing data from 8 sires were used to verify the presence of genomic variations within their flanking regions in 81.56% of these missing genotypes. Furthermore, we discovered 3,300 novel SNPs/Indels, 31% of which are located in genes that may affect traits of importance for the genetic improvement of cattle production.

Indexed as

Genetic VariationGenomeAnimalsBase PairingBreedingCattleChromosomes, MammalianGene OntologyGenetic MarkersGenotypeMolecular Sequence AnnotationOpen Reading FramesPolymorphism, Single NucleotideGenetic Markers

Identifiers

PMID26305794
PMCPMC4549312

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.