Evidence map›Paper›PMID 29940846›Full record

ArticleGenetics, selection, evolution : GSE2018

SNPrune: an efficient algorithm to prune large SNP array and sequence datasets based on high linkage disequilibrium.

Mario P L Calus, Jérémie Vandenplas

Open access · goldAbstract read
In one paragraph

Article in Genetics, selection, evolution : GSE, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.6field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 56 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Mario P L CalusAnimal Breeding and Genomics, Wageningen University & Research, P.O. Box 338, 6700 AH, Wageningen, The Netherlands. mario.calus@wur.nl.ORCID 0000-0002-3213-704X
Jérémie VandenplasAnimal Breeding and Genomics, Wageningen University & Research, P.O. Box 338, 6700 AH, Wageningen, The Netherlands.
Wageningen University & Research · NL

Funding

Dutch Ministry of Economic Affairs (TKI Agri & Food) 16022
6 · The paper itself

Abstract

backgroundHigh levels of pairwise linkage disequilibrium (LD) in single nucleotide polymorphism (SNP) array or whole-genome sequence data may affect both performance and efficiency of genomic prediction models. Thus, this warrants pruning of genotyping data for high LD. We developed an algorithm, named SNPrune, which enables the rapid detection of any pair of SNPs in complete or high LD throughout the genome.

methodsLD, measured as the squared correlation between phased alleles (r

resultsSNPrune removed a similar number of SNPs as PLINK from the pig data but SNPrune was almost 12 times faster than PLINK. From the simulated sequence data with 10.8 million SNPs, SNPrune removed 6.4 and 1.4 million SNPs due to complete and high LD. Results were very similar regardless of whether phased alleles or allele counts were used. Using allele counts and multi-threading with 10 threads, SNPrune completed the analysis in 21 min. Using a sliding window of up to 500,000 SNPs, PLINK removed ~ 43,000 less SNPs (0.6%) in the sequence data and SNPrune was 24 to 170 times faster, using one or ten threads, respectively.

conclusionsThe SNPrune algorithm developed here is able to remove SNPs in high LD throughout the genome very efficiently in large datasets.

Indexed as

AlgorithmsLinkage DisequilibriumAnimalsDatabases, GeneticModels, GeneticPolymorphism, Single NucleotideSwineWhole Genome Sequencing

Identifiers

PMID29940846
PMCPMC6019535
OpenAlexW2810856658

What OpenQuestion holds

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LicenceCC BY
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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.