Segtor: rapid annotation of genomic coordinates and single nucleotide variations using segment trees.

Various research projects often involve determining the relative position of genomic coordinates, intervals, single nucleotide variations (SNVs), insertions, deletions and translocations with respect to genes and their potential impact on protein translation. Due to the tremendous increase in throug...

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Autores principales:	Gabriel Renaud, Pedro Neves, Edson Luiz Folador, Carlos Gil Ferreira, Fabio Passetti
Formato:	article
Lenguaje:	EN
Publicado:	Public Library of Science (PLoS) 2011
Materias:	Medicine R Science Q
Acceso en línea:	https://doaj.org/article/fdc23b81580246979678e015369428fb
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spelling	oai:doaj.org-article:fdc23b81580246979678e015369428fb2021-11-18T07:35:17ZSegtor: rapid annotation of genomic coordinates and single nucleotide variations using segment trees.1932-620310.1371/journal.pone.0026715https://doaj.org/article/fdc23b81580246979678e015369428fb2011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22069465/?tool=EBIhttps://doaj.org/toc/1932-6203Various research projects often involve determining the relative position of genomic coordinates, intervals, single nucleotide variations (SNVs), insertions, deletions and translocations with respect to genes and their potential impact on protein translation. Due to the tremendous increase in throughput brought by the use of next-generation sequencing, investigators are routinely faced with the need to annotate very large datasets. We present Segtor, a tool to annotate large sets of genomic coordinates, intervals, SNVs, indels and translocations. Our tool uses segment trees built using the start and end coordinates of the genomic features the user wishes to use instead of storing them in a database management system. The software also produces annotation statistics to allow users to visualize how many coordinates were found within various portions of genes. Our system currently can be made to work with any species available on the UCSC Genome Browser. Segtor is a suitable tool for groups, especially those with limited access to programmers or with interest to analyze large amounts of individual genomes, who wish to determine the relative position of very large sets of mapped reads and subsequently annotate observed mutations between the reads and the reference. Segtor (http://lbbc.inca.gov.br/segtor/) is an open-source tool that can be freely downloaded for non-profit use. We also provide a web interface for testing purposes.Gabriel RenaudPedro NevesEdson Luiz FoladorCarlos Gil FerreiraFabio PassettiPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 11, p e26715 (2011)
institution	DOAJ
collection	DOAJ
language	EN
topic	Medicine R Science Q
spellingShingle	Medicine R Science Q Gabriel Renaud Pedro Neves Edson Luiz Folador Carlos Gil Ferreira Fabio Passetti Segtor: rapid annotation of genomic coordinates and single nucleotide variations using segment trees.
description	Various research projects often involve determining the relative position of genomic coordinates, intervals, single nucleotide variations (SNVs), insertions, deletions and translocations with respect to genes and their potential impact on protein translation. Due to the tremendous increase in throughput brought by the use of next-generation sequencing, investigators are routinely faced with the need to annotate very large datasets. We present Segtor, a tool to annotate large sets of genomic coordinates, intervals, SNVs, indels and translocations. Our tool uses segment trees built using the start and end coordinates of the genomic features the user wishes to use instead of storing them in a database management system. The software also produces annotation statistics to allow users to visualize how many coordinates were found within various portions of genes. Our system currently can be made to work with any species available on the UCSC Genome Browser. Segtor is a suitable tool for groups, especially those with limited access to programmers or with interest to analyze large amounts of individual genomes, who wish to determine the relative position of very large sets of mapped reads and subsequently annotate observed mutations between the reads and the reference. Segtor (http://lbbc.inca.gov.br/segtor/) is an open-source tool that can be freely downloaded for non-profit use. We also provide a web interface for testing purposes.
format	article
author	Gabriel Renaud Pedro Neves Edson Luiz Folador Carlos Gil Ferreira Fabio Passetti
author_facet	Gabriel Renaud Pedro Neves Edson Luiz Folador Carlos Gil Ferreira Fabio Passetti
author_sort	Gabriel Renaud
title	Segtor: rapid annotation of genomic coordinates and single nucleotide variations using segment trees.
title_short	Segtor: rapid annotation of genomic coordinates and single nucleotide variations using segment trees.
title_full	Segtor: rapid annotation of genomic coordinates and single nucleotide variations using segment trees.
title_fullStr	Segtor: rapid annotation of genomic coordinates and single nucleotide variations using segment trees.
title_full_unstemmed	Segtor: rapid annotation of genomic coordinates and single nucleotide variations using segment trees.
title_sort	segtor: rapid annotation of genomic coordinates and single nucleotide variations using segment trees.
publisher	Public Library of Science (PLoS)
publishDate	2011
url	https://doaj.org/article/fdc23b81580246979678e015369428fb
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Segtor: rapid annotation of genomic coordinates and single nucleotide variations using segment trees.

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