Evidence map›Paper›PMID 26303864›Full record

ArticleBMC genetics2015

Ridge, Lasso and Bayesian additive-dominance genomic models.

Camila Ferreira Azevedo, Marcos Deon Vilela de Resende, Fabyano Fonseca E Silva, José Marcelo Soriano Viana, Magno Sávio Ferreira Valente, Márcio Fernando Ribeiro Resende, Patricio Muñoz

Abstract read
In one paragraph

Article in BMC genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Using visual scores for genomic prediction of complex traits in breeding programs.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Relationship between SNPs ofAnimals : an open access journal from MDPI · 2019
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Non-additive Effects in Genomic Selection.Frontiers in genetics · 2018
    Review
  20. Multienvironment genomic variance decomposition analysis of open-pollinated Interior spruce (Molecular breeding : new strategies in plant improvement · 2018
    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.

Camila Ferreira AzevedoDepartment of Statistics, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil. camila.azevedo@ufv.br.
Marcos Deon Vilela de ResendeDepartment of Statistics, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil. marcos.deon@gmail.com.
Fabyano Fonseca E SilvaDepartment of Animal Science, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil. fabyanofonseca@ufv.br.
José Marcelo Soriano VianaDepartment of General Biology, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil. jmsviana@ufv.br.
Magno Sávio Ferreira ValenteDepartment of General Biology, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil. magnosavio@yahoo.com.br.
Márcio Fernando Ribeiro ResendeRAPiD Genomics, Florida Innovation Hub, Gainesville, Florida, USA. mresende@rapid-genomics.com.
Patricio MuñozAgronomy Department, University of Florida, Gainesville, Florida, USA. pmdelvalle@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA complete approach for genome-wide selection (GWS) involves reliable statistical genetics models and methods. Reports on this topic are common for additive genetic models but not for additive-dominance models. The objective of this paper was (i) to compare the performance of 10 additive-dominance predictive models (including current models and proposed modifications), fitted using Bayesian, Lasso and Ridge regression approaches; and (ii) to decompose genomic heritability and accuracy in terms of three quantitative genetic information sources, namely, linkage disequilibrium (LD), co-segregation (CS) and pedigree relationships or family structure (PR). The simulation study considered two broad sense heritability levels (0.30 and 0.50, associated with narrow sense heritabilities of 0.20 and 0.35, respectively) and two genetic architectures for traits (the first consisting of small gene effects and the second consisting of a mixed inheritance model with five major genes).

resultsG-REML/G-BLUP and a modified Bayesian/Lasso (called BayesA*B* or t-BLASSO) method performed best in the prediction of genomic breeding as well as the total genotypic values of individuals in all four scenarios (two heritabilities x two genetic architectures). The BayesA*B*-type method showed a better ability to recover the dominance variance/additive variance ratio. Decomposition of genomic heritability and accuracy revealed the following descending importance order of information: LD, CS and PR not captured by markers, the last two being very close.

conclusionsAmongst the 10 models/methods evaluated, the G-BLUP, BAYESA*B* (-2,8) and BAYESA*B* (4,6) methods presented the best results and were found to be adequate for accurately predicting genomic breeding and total genotypic values as well as for estimating additive and dominance in additive-dominance genomic models.

Indexed as

Genes, DominantModels, GeneticModels, StatisticalAlgorithmsGenome-Wide Association StudyQuantitative Trait LociReproducibility of ResultsSelection, Genetic

Identifiers

PMID26303864
PMCPMC4549024

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.