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Exploiting the great potential of Sequence Capture data by a new tool, SUPER-CAP

The recent development of Sequence Capture methodology represents a powerful strategy for enhancing data generation to assess genetic variation of targeted genomic regions. Here, we present SUPER-CAP, a bioinformatics web tool aimed at handling Sequence Capture data, fine calculating the allele freq...

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Autores principales: Ruggieri, Valentino, Anzar, Irantzu, Paytuvi, Andreu, Calafiore, Roberta, Cigliano, Riccardo Aiese, Sanseverino, Walter, Barone, Amalia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381350/
https://www.ncbi.nlm.nih.gov/pubmed/28011720
http://dx.doi.org/10.1093/dnares/dsw050
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author Ruggieri, Valentino
Anzar, Irantzu
Paytuvi, Andreu
Calafiore, Roberta
Cigliano, Riccardo Aiese
Sanseverino, Walter
Barone, Amalia
author_facet Ruggieri, Valentino
Anzar, Irantzu
Paytuvi, Andreu
Calafiore, Roberta
Cigliano, Riccardo Aiese
Sanseverino, Walter
Barone, Amalia
author_sort Ruggieri, Valentino
collection PubMed
description The recent development of Sequence Capture methodology represents a powerful strategy for enhancing data generation to assess genetic variation of targeted genomic regions. Here, we present SUPER-CAP, a bioinformatics web tool aimed at handling Sequence Capture data, fine calculating the allele frequency of variations and building genotype-specific sequence of captured genes. The dataset used to develop this in silico strategy consists of 378 loci and related regulative regions in a collection of 44 tomato landraces. About 14,000 high-quality variants were identified. The high depth (>40×) of coverage and adopting the correct filtering criteria allowed identification of about 4,000 rare variants and 10 genes with a different copy number variation. We also show that the tool is capable to reconstruct genotype-specific sequences for each genotype by using the detected variants. This allows evaluating the combined effect of multiple variants in the same protein. The architecture and functionality of SUPER-CAP makes the software appropriate for a broad set of analyses including SNP discovery and mining. Its functionality, together with the capability to process large data sets and efficient detection of sequence variation, makes SUPER-CAP a valuable bioinformatics tool for genomics and breeding purposes.
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spelling pubmed-53813502017-04-10 Exploiting the great potential of Sequence Capture data by a new tool, SUPER-CAP Ruggieri, Valentino Anzar, Irantzu Paytuvi, Andreu Calafiore, Roberta Cigliano, Riccardo Aiese Sanseverino, Walter Barone, Amalia DNA Res Full Papers The recent development of Sequence Capture methodology represents a powerful strategy for enhancing data generation to assess genetic variation of targeted genomic regions. Here, we present SUPER-CAP, a bioinformatics web tool aimed at handling Sequence Capture data, fine calculating the allele frequency of variations and building genotype-specific sequence of captured genes. The dataset used to develop this in silico strategy consists of 378 loci and related regulative regions in a collection of 44 tomato landraces. About 14,000 high-quality variants were identified. The high depth (>40×) of coverage and adopting the correct filtering criteria allowed identification of about 4,000 rare variants and 10 genes with a different copy number variation. We also show that the tool is capable to reconstruct genotype-specific sequences for each genotype by using the detected variants. This allows evaluating the combined effect of multiple variants in the same protein. The architecture and functionality of SUPER-CAP makes the software appropriate for a broad set of analyses including SNP discovery and mining. Its functionality, together with the capability to process large data sets and efficient detection of sequence variation, makes SUPER-CAP a valuable bioinformatics tool for genomics and breeding purposes. Oxford University Press 2017-02 2016-12-08 /pmc/articles/PMC5381350/ /pubmed/28011720 http://dx.doi.org/10.1093/dnares/dsw050 Text en © The Author 2016. Published by Oxford University Press on behalf of Kazusa DNA Research Institute. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Full Papers
Ruggieri, Valentino
Anzar, Irantzu
Paytuvi, Andreu
Calafiore, Roberta
Cigliano, Riccardo Aiese
Sanseverino, Walter
Barone, Amalia
Exploiting the great potential of Sequence Capture data by a new tool, SUPER-CAP
title Exploiting the great potential of Sequence Capture data by a new tool, SUPER-CAP
title_full Exploiting the great potential of Sequence Capture data by a new tool, SUPER-CAP
title_fullStr Exploiting the great potential of Sequence Capture data by a new tool, SUPER-CAP
title_full_unstemmed Exploiting the great potential of Sequence Capture data by a new tool, SUPER-CAP
title_short Exploiting the great potential of Sequence Capture data by a new tool, SUPER-CAP
title_sort exploiting the great potential of sequence capture data by a new tool, super-cap
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381350/
https://www.ncbi.nlm.nih.gov/pubmed/28011720
http://dx.doi.org/10.1093/dnares/dsw050
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