Evidence map›Paper›PMID 36936433›Full record

ArticleFrontiers in genetics2023

Smooth Descent: A ploidy-aware algorithm to improve linkage mapping in the presence of genotyping errors.

Alejandro Thérèse Navarro, Peter M Bourke, Eric van de Weg, Corentin R Clot, Paul Arens, Richard Finkers, Chris Maliepaard

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Article in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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3 citing papers in PubMed.

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5 · Who and what money

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7 authors.

Alejandro Thérèse NavarroPlant Breeding, Wageningen University & Research, Wageningen, Netherlands.
Peter M BourkePlant Breeding, Wageningen University & Research, Wageningen, Netherlands.
Eric van de WegPlant Breeding, Wageningen University & Research, Wageningen, Netherlands.
Corentin R ClotPlant Breeding, Wageningen University & Research, Wageningen, Netherlands.
Paul ArensPlant Breeding, Wageningen University & Research, Wageningen, Netherlands.
Richard FinkersPlant Breeding, Wageningen University & Research, Wageningen, Netherlands.
Chris MaliepaardPlant Breeding, Wageningen University & Research, Wageningen, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Linkage mapping is an approach to order markers based on recombination events. Mapping algorithms cannot easily handle genotyping errors, which are common in high-throughput genotyping data. To solve this issue, strategies have been developed, aimed mostly at identifying and eliminating these errors. One such strategy is SMOOTH, an iterative algorithm to detect genotyping errors. Unlike other approaches, SMOOTH can also be used to impute the most probable alternative genotypes, but its application is limited to diploid species and to markers heterozygous in only one of the parents. In this study we adapted SMOOTH to expand its use to any marker type and to autopolyploids with the use of identity-by-descent probabilities, naming the updated algorithm Smooth Descent (SD). We applied SD to real and simulated data, showing that in the presence of genotyping errors this method produces better genetic maps in terms of marker order and map length. SD is particularly useful for error rates between 5% and 20% and when error rates are not homogeneous among markers or individuals. With a starting error rate of 10%, SD reduced it to ∼5% in diploids, ∼7% in tetraploids and ∼8.5% in hexaploids. Conversely, the correlation between true and estimated genetic maps increased by 0.03 in tetraploids and by 0.2 in hexaploids, while worsening slightly in diploids (∼0.0011). We also show that the combination of genotype curation and map re-estimation allowed us to obtain better genetic maps while correcting wrong genotypes. We have implemented this algorithm in the R package Smooth Descent.

Indexed as

genotyping erroridentity by descentimputationlinkage mappingpolyploidy

Identifiers

PMID36936433
PMCPMC10014611

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