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Article: SLRfinder: A method to detect candidate sex-linked regions with linkage disequilibrium clustering

TitleSLRfinder: A method to detect candidate sex-linked regions with linkage disequilibrium clustering
Authors
Keywordsheterozygosity
inversion
LD
sex chromosomes
sex-determining region
SLR
Issue Date8-Jun-2024
PublisherWiley
Citation
Molecular Ecology Resources, 2024, v. 24, n. 6 How to Cite?
AbstractDespite their critical roles in genetic sex determination, sex chromosomes remain unknown in many non-model organisms, especially those having recently evolved sex-linked regions (SLRs). These evolutionarily young and labile sex chromosomes are important for understanding early sex chromosome evolution but are difficult to identify due to the lack of Y/W degeneration and SLRs limited to small genomic regions. Here, we present SLRfinder, a method to identify candidate SLRs using linkage disequilibrium (LD) clustering, heterozygosity and genetic divergence. SLRfinder does not rely on specific sequencing methods or a specific type of reference genome (e.g., from the homomorphic sex). In addition, the input of SLRfinder does not require phenotypic sexes, which may be unknown from population sampling, but sex information can be incorporated and is necessary to validate candidate SLRs. We tested SLRfinder using various published datasets and compared it to the local principal component analysis (PCA) method and the depth-based method Sex Assignment Through Coverage (SATC). As expected, the local PCA method could not be used to identify unknown SLRs. SATC works better on conserved sex chromosomes, whereas SLRfinder outperforms SATC in analysing labile sex chromosomes, especially when SLRs harbour inversions. Power analyses showed that SLRfinder worked better when sampling more populations that share the same SLR. If analysing one population, a relatively larger sample size (around 50) is needed for sufficient statistical power to detect significant SLR candidates, although true SLRs are likely always top-ranked. SLRfinder provides a novel and complementary approach for identifying SLRs and uncovering additional sex chromosome diversity in nature.
Persistent Identifierhttp://hdl.handle.net/10722/347806
ISSN
2023 Impact Factor: 5.5
2023 SCImago Journal Rankings: 2.465

 

DC FieldValueLanguage
dc.contributor.authorYi, Xueling-
dc.contributor.authorKemppainen, Petri-
dc.contributor.authorMerilä, Juha-
dc.date.accessioned2024-09-29T00:30:28Z-
dc.date.available2024-09-29T00:30:28Z-
dc.date.issued2024-06-08-
dc.identifier.citationMolecular Ecology Resources, 2024, v. 24, n. 6-
dc.identifier.issn1755-098X-
dc.identifier.urihttp://hdl.handle.net/10722/347806-
dc.description.abstractDespite their critical roles in genetic sex determination, sex chromosomes remain unknown in many non-model organisms, especially those having recently evolved sex-linked regions (SLRs). These evolutionarily young and labile sex chromosomes are important for understanding early sex chromosome evolution but are difficult to identify due to the lack of Y/W degeneration and SLRs limited to small genomic regions. Here, we present SLRfinder, a method to identify candidate SLRs using linkage disequilibrium (LD) clustering, heterozygosity and genetic divergence. SLRfinder does not rely on specific sequencing methods or a specific type of reference genome (e.g., from the homomorphic sex). In addition, the input of SLRfinder does not require phenotypic sexes, which may be unknown from population sampling, but sex information can be incorporated and is necessary to validate candidate SLRs. We tested SLRfinder using various published datasets and compared it to the local principal component analysis (PCA) method and the depth-based method Sex Assignment Through Coverage (SATC). As expected, the local PCA method could not be used to identify unknown SLRs. SATC works better on conserved sex chromosomes, whereas SLRfinder outperforms SATC in analysing labile sex chromosomes, especially when SLRs harbour inversions. Power analyses showed that SLRfinder worked better when sampling more populations that share the same SLR. If analysing one population, a relatively larger sample size (around 50) is needed for sufficient statistical power to detect significant SLR candidates, although true SLRs are likely always top-ranked. SLRfinder provides a novel and complementary approach for identifying SLRs and uncovering additional sex chromosome diversity in nature.-
dc.languageeng-
dc.publisherWiley-
dc.relation.ispartofMolecular Ecology Resources-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectheterozygosity-
dc.subjectinversion-
dc.subjectLD-
dc.subjectsex chromosomes-
dc.subjectsex-determining region-
dc.subjectSLR-
dc.titleSLRfinder: A method to detect candidate sex-linked regions with linkage disequilibrium clustering-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1111/1755-0998.13985-
dc.identifier.pmid38850116-
dc.identifier.scopuseid_2-s2.0-85195551686-
dc.identifier.volume24-
dc.identifier.issue6-
dc.identifier.eissn1755-0998-
dc.identifier.issnl1755-098X-

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