Evidence map›Paper›PMID 32039696›Full record

ArticleGenetics, selection, evolution : GSE2020

SeqBreed: a python tool to evaluate genomic prediction in complex scenarios.

Miguel Pérez-Enciso, Lino C Ramírez-Ayala, Laura M Zingaretti

Abstract readEvaluation Study
In one paragraph

Article in Genetics, selection, evolution : GSE, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Bridging tradition and innovation: a review of computer simulations in plant breeding.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2026
    Review
  2. Review
  3. Article
  4. Computational tools for plant genomics and breeding.Science China. Life sciences · 2024
    Review
  5. Article
  6. Article
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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

3 authors.

Miguel Pérez-EncisoCentre for Research in Agricultural Genomics (CRAG), CSIC-IRTA-UAB-UB, 08193, Bellaterra, Barcelona, Spain. miguel.perez@uab.es.ORCID http://orcid.org/0000-0003-3524-995X
Lino C Ramírez-AyalaCentre for Research in Agricultural Genomics (CRAG), CSIC-IRTA-UAB-UB, 08193, Bellaterra, Barcelona, Spain.
Laura M ZingarettiCentre for Research in Agricultural Genomics (CRAG), CSIC-IRTA-UAB-UB, 08193, Bellaterra, Barcelona, Spain.ORCID http://orcid.org/0000-0001-5618-2630

Funding

MINECO AGL2016-78709-R
6 · The paper itself

Abstract

backgroundGenomic prediction (GP) is a method whereby DNA polymorphism information is used to predict breeding values for complex traits. Although GP can significantly enhance predictive accuracy, it can be expensive and difficult to implement. To help design optimum breeding programs and experiments, including genome-wide association studies and genomic selection experiments, we have developed SeqBreed, a generic and flexible forward simulator programmed in python3.

resultsSeqBreed accommodates sex and mitochondrion chromosomes as well as autopolyploidy. It can simulate any number of complex phenotypes that are determined by any number of causal loci. SeqBreed implements several GP methods, including genomic best linear unbiased prediction (GBLUP), single-step GBLUP, pedigree-based BLUP, and mass selection. We illustrate its functionality with Drosophila genome reference panel (DGRP) sequence data and with tetraploid potato genotype data.

conclusionsSeqBreed is a flexible and easy to use tool that can be used to optimize GP or genome-wide association studies. It incorporates some of the most popular GP methods and includes several visualization tools. Code is open and can be freely modified. Software, documentation, and examples are available at https://github.com/miguelperezenciso/SeqBreed.

Indexed as

AnimalsBreedingDrosophilaFemaleGenome-Wide Association StudyGenomicsGenotypeMaleMultifactorial InheritancePedigreeSoftware

Identifiers

PMID32039696
PMCPMC7008576

What OpenQuestion holds

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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.