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CLARITY: a Shiny app for interactive visualisation of the bovine physical-genetic map

The arrangement of markers on the genome can be defined in either physical or linkage terms. While a physical map represents the inter-marker distances in base pairs, a genetic (or linkage) map pictures the recombination rate between pairs of markers. High-resolution genetic maps are key elements fo...

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Autores principales: Melzer, Nina, Qanbari, Saber, Ding, Xi, Wittenburg, Dörte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267868/
https://www.ncbi.nlm.nih.gov/pubmed/37323679
http://dx.doi.org/10.3389/fgene.2023.1082782
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author Melzer, Nina
Qanbari, Saber
Ding, Xi
Wittenburg, Dörte
author_facet Melzer, Nina
Qanbari, Saber
Ding, Xi
Wittenburg, Dörte
author_sort Melzer, Nina
collection PubMed
description The arrangement of markers on the genome can be defined in either physical or linkage terms. While a physical map represents the inter-marker distances in base pairs, a genetic (or linkage) map pictures the recombination rate between pairs of markers. High-resolution genetic maps are key elements for genomic research, such as fine-mapping of quantitative trait loci, but they are also needed for creating and updating chromosome-level assemblies of whole-genome sequences. Based on published results on a large pedigree of German Holstein cattle and newly obtained results with German/Austrian Fleckvieh cattle, we aim at providing a platform that allows users to interactively explore the bovine genetic and physical map. We developed the R Shiny app CLARITY available online at https://nmelzer.shinyapps.io/clarity and as R package at https://github.com/nmelzer/CLARITY that provides access to the genetic maps built on the Illumina Bovine SNP50 genotyping array with markers ordered according to the physical coordinates of the most recent bovine genome assembly ARS-UCD1.2. The user is able to interconnect the physical and genetic map for a whole chromosome or a specific chromosomal region and can inspect a landscape of recombination hotspots. Moreover, the user can investigate which of the frequently used genetic-map functions locally fits best. We further provide auxiliary information about markers being putatively misplaced in the ARS-UCD1.2 release. The corresponding output tables and figures can be downloaded in various formats. By ongoing data integration from different breeds, the app also facilitates comparison of different genome features, providing a valuable tool for education and research purposes.
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spelling pubmed-102678682023-06-15 CLARITY: a Shiny app for interactive visualisation of the bovine physical-genetic map Melzer, Nina Qanbari, Saber Ding, Xi Wittenburg, Dörte Front Genet Genetics The arrangement of markers on the genome can be defined in either physical or linkage terms. While a physical map represents the inter-marker distances in base pairs, a genetic (or linkage) map pictures the recombination rate between pairs of markers. High-resolution genetic maps are key elements for genomic research, such as fine-mapping of quantitative trait loci, but they are also needed for creating and updating chromosome-level assemblies of whole-genome sequences. Based on published results on a large pedigree of German Holstein cattle and newly obtained results with German/Austrian Fleckvieh cattle, we aim at providing a platform that allows users to interactively explore the bovine genetic and physical map. We developed the R Shiny app CLARITY available online at https://nmelzer.shinyapps.io/clarity and as R package at https://github.com/nmelzer/CLARITY that provides access to the genetic maps built on the Illumina Bovine SNP50 genotyping array with markers ordered according to the physical coordinates of the most recent bovine genome assembly ARS-UCD1.2. The user is able to interconnect the physical and genetic map for a whole chromosome or a specific chromosomal region and can inspect a landscape of recombination hotspots. Moreover, the user can investigate which of the frequently used genetic-map functions locally fits best. We further provide auxiliary information about markers being putatively misplaced in the ARS-UCD1.2 release. The corresponding output tables and figures can be downloaded in various formats. By ongoing data integration from different breeds, the app also facilitates comparison of different genome features, providing a valuable tool for education and research purposes. Frontiers Media S.A. 2023-05-30 /pmc/articles/PMC10267868/ /pubmed/37323679 http://dx.doi.org/10.3389/fgene.2023.1082782 Text en Copyright © 2023 Melzer, Qanbari, Ding and Wittenburg. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Melzer, Nina
Qanbari, Saber
Ding, Xi
Wittenburg, Dörte
CLARITY: a Shiny app for interactive visualisation of the bovine physical-genetic map
title CLARITY: a Shiny app for interactive visualisation of the bovine physical-genetic map
title_full CLARITY: a Shiny app for interactive visualisation of the bovine physical-genetic map
title_fullStr CLARITY: a Shiny app for interactive visualisation of the bovine physical-genetic map
title_full_unstemmed CLARITY: a Shiny app for interactive visualisation of the bovine physical-genetic map
title_short CLARITY: a Shiny app for interactive visualisation of the bovine physical-genetic map
title_sort clarity: a shiny app for interactive visualisation of the bovine physical-genetic map
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267868/
https://www.ncbi.nlm.nih.gov/pubmed/37323679
http://dx.doi.org/10.3389/fgene.2023.1082782
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