A unique, consistent identifier for alternatively spliced transcript variants.

As research into alternative splicing reveals the fundamental importance of this phenomenon in the genome expression of higher organisms, there is an increasing need for a standardized, consistent and unique identifier for alternatively spliced isoforms. Such an identifier would be useful to elimina...

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Main Authors: Alberto Riva, Graziano Pesole
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-10-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2765725?pdf=render
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spelling doaj-ec9a3afa284e433c85f235ca1aaacd0a2020-11-25T00:44:18ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-10-01410e763110.1371/journal.pone.0007631A unique, consistent identifier for alternatively spliced transcript variants.Alberto RivaGraziano PesoleAs research into alternative splicing reveals the fundamental importance of this phenomenon in the genome expression of higher organisms, there is an increasing need for a standardized, consistent and unique identifier for alternatively spliced isoforms. Such an identifier would be useful to eliminate ambiguities in references to gene isoforms, and would allow for the reliable comparison of isoforms from different sources (e.g., known genes vs. computational predictions). Commonly used identifiers for gene transcripts prove to be unsuitable for this purpose.We propose an algorithm to compute an isoform signature based on the arrangement of exons and introns in a primary transcript. The isoform signature uniquely identifies a transcript structure, and can therefore be used as a key in databases of alternatively spliced isoforms, or to compare alternative splicing predictions produced by different methods. In this paper we present the algorithm to generate isoform signatures, we provide some examples of its application, and we describe a web-based resource to generate isoform signatures and use them in database searches.Isoform signatures are simple, so that they can be easily generated and included in publications and databases, but flexible enough to unambiguously represent all possible isoform structures, including information about coding sequence position and variable transcription start and end sites. We believe that the adoption of isoform signatures can help establish a consistent, unambiguous nomenclature for alternative splicing isoforms. The system described in this paper is freely available at http://genome.ufl.edu/genesig/, and supplementary materials can be found at http://genome.ufl.edu/genesig-files/.http://europepmc.org/articles/PMC2765725?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Alberto Riva
Graziano Pesole
spellingShingle Alberto Riva
Graziano Pesole
A unique, consistent identifier for alternatively spliced transcript variants.
PLoS ONE
author_facet Alberto Riva
Graziano Pesole
author_sort Alberto Riva
title A unique, consistent identifier for alternatively spliced transcript variants.
title_short A unique, consistent identifier for alternatively spliced transcript variants.
title_full A unique, consistent identifier for alternatively spliced transcript variants.
title_fullStr A unique, consistent identifier for alternatively spliced transcript variants.
title_full_unstemmed A unique, consistent identifier for alternatively spliced transcript variants.
title_sort unique, consistent identifier for alternatively spliced transcript variants.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2009-10-01
description As research into alternative splicing reveals the fundamental importance of this phenomenon in the genome expression of higher organisms, there is an increasing need for a standardized, consistent and unique identifier for alternatively spliced isoforms. Such an identifier would be useful to eliminate ambiguities in references to gene isoforms, and would allow for the reliable comparison of isoforms from different sources (e.g., known genes vs. computational predictions). Commonly used identifiers for gene transcripts prove to be unsuitable for this purpose.We propose an algorithm to compute an isoform signature based on the arrangement of exons and introns in a primary transcript. The isoform signature uniquely identifies a transcript structure, and can therefore be used as a key in databases of alternatively spliced isoforms, or to compare alternative splicing predictions produced by different methods. In this paper we present the algorithm to generate isoform signatures, we provide some examples of its application, and we describe a web-based resource to generate isoform signatures and use them in database searches.Isoform signatures are simple, so that they can be easily generated and included in publications and databases, but flexible enough to unambiguously represent all possible isoform structures, including information about coding sequence position and variable transcription start and end sites. We believe that the adoption of isoform signatures can help establish a consistent, unambiguous nomenclature for alternative splicing isoforms. The system described in this paper is freely available at http://genome.ufl.edu/genesig/, and supplementary materials can be found at http://genome.ufl.edu/genesig-files/.
url http://europepmc.org/articles/PMC2765725?pdf=render
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