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Accelerating structure‐function mapping using the ViVa webtool to mine natural variation
Thousands of sequenced genomes are now publicly available capturing a significant amount of natural variation within plant species; yet, much of these data remain inaccessible to researchers without significant bioinformatics experience. Here, we present a webtool called ViVa (Visualizing Variation)...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6658840/ https://www.ncbi.nlm.nih.gov/pubmed/31372596 http://dx.doi.org/10.1002/pld3.147 |
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author | Hamm, Morgan O. Moss, Britney L. Leydon, Alexander R. Gala, Hardik P. Lanctot, Amy Ramos, Román Klaeser, Hannah Lemmex, Andrew C. Zahler, Mollye L. Nemhauser, Jennifer L. Wright, R. Clay |
author_facet | Hamm, Morgan O. Moss, Britney L. Leydon, Alexander R. Gala, Hardik P. Lanctot, Amy Ramos, Román Klaeser, Hannah Lemmex, Andrew C. Zahler, Mollye L. Nemhauser, Jennifer L. Wright, R. Clay |
author_sort | Hamm, Morgan O. |
collection | PubMed |
description | Thousands of sequenced genomes are now publicly available capturing a significant amount of natural variation within plant species; yet, much of these data remain inaccessible to researchers without significant bioinformatics experience. Here, we present a webtool called ViVa (Visualizing Variation) which aims to empower any researcher to take advantage of the amazing genetic resource collected in the Arabidopsis thaliana 1001 Genomes Project (http://1001genomes.org). ViVa facilitates data mining on the gene, gene family, or gene network level. To test the utility and accessibility of ViVa, we assembled a team with a range of expertise within biology and bioinformatics to analyze the natural variation within the well‐studied nuclear auxin signaling pathway. Our analysis has provided further confirmation of existing knowledge and has also helped generate new hypotheses regarding this well‐studied pathway. These results highlight how natural variation could be used to generate and test hypotheses about less‐studied gene families and networks, especially when paired with biochemical and genetic characterization. ViVa is also readily extensible to databases of interspecific genetic variation in plants as well as other organisms, such as the 3,000 Rice Genomes Project ( http://snp-seek.irri.org/) and human genetic variation ( https://www.ncbi.nlm.nih.gov/clinvar/). |
format | Online Article Text |
id | pubmed-6658840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66588402019-08-01 Accelerating structure‐function mapping using the ViVa webtool to mine natural variation Hamm, Morgan O. Moss, Britney L. Leydon, Alexander R. Gala, Hardik P. Lanctot, Amy Ramos, Román Klaeser, Hannah Lemmex, Andrew C. Zahler, Mollye L. Nemhauser, Jennifer L. Wright, R. Clay Plant Direct Original Research Thousands of sequenced genomes are now publicly available capturing a significant amount of natural variation within plant species; yet, much of these data remain inaccessible to researchers without significant bioinformatics experience. Here, we present a webtool called ViVa (Visualizing Variation) which aims to empower any researcher to take advantage of the amazing genetic resource collected in the Arabidopsis thaliana 1001 Genomes Project (http://1001genomes.org). ViVa facilitates data mining on the gene, gene family, or gene network level. To test the utility and accessibility of ViVa, we assembled a team with a range of expertise within biology and bioinformatics to analyze the natural variation within the well‐studied nuclear auxin signaling pathway. Our analysis has provided further confirmation of existing knowledge and has also helped generate new hypotheses regarding this well‐studied pathway. These results highlight how natural variation could be used to generate and test hypotheses about less‐studied gene families and networks, especially when paired with biochemical and genetic characterization. ViVa is also readily extensible to databases of interspecific genetic variation in plants as well as other organisms, such as the 3,000 Rice Genomes Project ( http://snp-seek.irri.org/) and human genetic variation ( https://www.ncbi.nlm.nih.gov/clinvar/). John Wiley and Sons Inc. 2019-07-26 /pmc/articles/PMC6658840/ /pubmed/31372596 http://dx.doi.org/10.1002/pld3.147 Text en © 2019 The Authors. Plant Direct published by American Society of Plant Biologists, Society for Experimental Biology and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Research Hamm, Morgan O. Moss, Britney L. Leydon, Alexander R. Gala, Hardik P. Lanctot, Amy Ramos, Román Klaeser, Hannah Lemmex, Andrew C. Zahler, Mollye L. Nemhauser, Jennifer L. Wright, R. Clay Accelerating structure‐function mapping using the ViVa webtool to mine natural variation |
title | Accelerating structure‐function mapping using the ViVa webtool to mine natural variation |
title_full | Accelerating structure‐function mapping using the ViVa webtool to mine natural variation |
title_fullStr | Accelerating structure‐function mapping using the ViVa webtool to mine natural variation |
title_full_unstemmed | Accelerating structure‐function mapping using the ViVa webtool to mine natural variation |
title_short | Accelerating structure‐function mapping using the ViVa webtool to mine natural variation |
title_sort | accelerating structure‐function mapping using the viva webtool to mine natural variation |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6658840/ https://www.ncbi.nlm.nih.gov/pubmed/31372596 http://dx.doi.org/10.1002/pld3.147 |
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