ASTD: The Alternative Splicing and Transcript Diversity database

84Citations
Citations of this article
119Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

The Alternative Splicing and Transcript Diversity database (ASTD) gives access to a vast collection of alternative transcripts that integrate transcription initiation, polyadenylation and splicing variant data. Alternative transcripts are derived from the mapping of transcribed sequences to the complete human, mouse and rat genomes using an extension of the computational pipeline developed for the ASD (Alternative Splicing Database) and ATD (Alternative Transcript Diversity) databases, which are now superseded by ASTD. For the human genome, ASTD identifies splicing variants, transcription initiation variants and polyadenylation variants in 68%, 68% and 62% of the gene set, respectively, consistent with current estimates for transcription variation. Users can access ASTD through a variety of browsing and query tools, including expression state-based queries for the identification of tissue-specific isoforms. Participating laboratories have experimentally validated a subset of ASTD-predicted alternative splice forms and alternative polyadenylation forms that were not previously reported. The ASTD database can be accessed at http://www.ebi.ac.uk/astd. © 2008 Elsevier Inc. All rights reserved.

Cite

CITATION STYLE

APA

Koscielny, G., Texier, V. L., Gopalakrishnan, C., Kumanduri, V., Riethoven, J. J., Nardone, F., … Gautheret, D. (2009). ASTD: The Alternative Splicing and Transcript Diversity database. Genomics, 93(3), 213–220. https://doi.org/10.1016/j.ygeno.2008.11.003

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free