Evidence map›Paper›PMID 38430392›Full record

ArticleTAG. Theoretical and applied genetics. Theoretische und angewandte Genetik2024

Construction of relatedness matrices in autopolyploid populations using low-depth high-throughput sequencing data.

Timothy P Bilton, Sanjeev Kumar Sharma, Matthew R Schofield, Michael A Black, Jeanne M E Jacobs, Glenn J Bryan, Ken G Dodds

Open access · hybridAbstract read
In one paragraph

Article in TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 2024. 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
1.2field-weighted citation impact, top 18% of its field
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, 2 citations in OpenAlex.

  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 at 3 institutions in 2 countries.

Timothy P BiltonAgResearch, Invermay Agricultural Centre, Mosgiel, New Zealand. timothy.bilton@agresearch.co.nz.ORCID http://orcid.org/0000-0001-5945-3766
Sanjeev Kumar SharmaCell and Molecular Sciences, The James Hutton Institute, Invergowrie, Dundee, UK.
Matthew R SchofieldDepartment of Mathematics and Statistics, University of Otago, Dunedin, New Zealand.ORCID http://orcid.org/0000-0003-1481-2766
Michael A BlackDepartment of Biochemistry, University of Otago, Dunedin, New Zealand.
Jeanne M E JacobsAgResearch, Lincoln Science Centre, Christchurch, New Zealand.ORCID http://orcid.org/0000-0002-1047-1039
Glenn J BryanCell and Molecular Sciences, The James Hutton Institute, Invergowrie, Dundee, UK.
Ken G DoddsAgResearch, Invermay Agricultural Centre, Mosgiel, New Zealand.ORCID http://orcid.org/0000-0002-9347-6379
AgResearch · NZJames Hutton Institute · GBUniversity of Otago · NZ

Funding

Ministry of Business, Innovation and Employment C10X1306Ministry of Business, Innovation and Employment Strategic Science Investment FundRural and Environment Science and Analytical Services Division Strategic Research Programme 2016 - 2021University of Otago Doctoral Scholarship
6 · The paper itself

Abstract

key messageAn improved estimator of genomic relatedness using low-depth high-throughput sequencing data for autopolyploids is developed. Its outputs strongly correlate with SNP array-based estimates and are available in the package GUSrelate. High-throughput sequencing (HTS) methods have reduced sequencing costs and resources compared to array-based tools, facilitating the investigation of many non-model polyploid species. One important quantity that can be computed from HTS data is the genetic relatedness between all individuals in a population. However, HTS data are often messy, with multiple sources of errors (i.e. sequencing errors or missing parental alleles) which, if not accounted for, can lead to bias in genomic relatedness estimates. We derive a new estimator for constructing a genomic relationship matrix (GRM) from HTS data for autopolyploid species that accounts for errors associated with low sequencing depths, implemented in the R package GUSrelate. Simulations revealed that GUSrelate performed similarly to existing GRM methods at high depth but reduced bias in self-relatedness estimates when the sequencing depth was low. Using a panel consisting of 351 tetraploid potato genotypes, we found that GUSrelate produced GRMs from genotyping-by-sequencing (GBS) data that were highly correlated with a GRM computed from SNP array data, and less biased than existing methods when benchmarking against the array-based GRM estimates. GUSrelate provides researchers with a tool to reliably construct GRMs from low-depth HTS data.

Indexed as

Genotyping TechniquesPolymorphism, Single NucleotideAllelesHigh-Throughput Nucleotide SequencingHumansSequence Analysis, DNA

Identifiers

PMID38430392
PMCPMC10908621
OpenAlexW4392348463

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.