Evidence map›Paper›PMID 16556303›Full record

ArticleBMC bioinformatics2006

AltTrans: transcript pattern variants annotated for both alternative splicing and alternative polyadenylation.

Vincent Le Texier, Jean-Jack Riethoven, Vasudev Kumanduri, Chellappa Gopalakrishnan, Fabrice Lopez, Daniel Gautheret, Thangavel Alphonse Thanaraj

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Article in BMC bioinformatics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

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20citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

20 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. TopHat: discovering splice junctions with RNA-Seq.Bioinformatics (Oxford, England) · 2009
    Article
  9. Article
  10. Article
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  12. Article
  13. Article
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  15. The Schistosoma mansoni transcriptome: an update.Experimental parasitology · 2007
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Vincent Le TexierEuropean Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SD, UK. texier@ebi.ac.uk
Jean-Jack Riethoven
Vasudev Kumanduri
Chellappa Gopalakrishnan
Fabrice Lopez
Daniel Gautheret
Thangavel Alphonse Thanaraj

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe three major mechanisms that regulate transcript formation involve the selection of alternative sites for transcription start (TS), splicing, and polyadenylation. Currently there are efforts that collect data & annotation individually for each of these variants. It is important to take an integrated view of these data sets and to derive a data set of alternate transcripts along with consolidated annotation. We have been developing in the past computational pipelines that generate value-added data at genome-scale on individual variant types; these include AltSplice on splicing and AltPAS on polyadenylation. We now extend these pipelines and integrate the resultant data sets to facilitate an integrated view of the contributions from splicing and polyadenylation in the formation of transcript variants. DESCRIPTION: The AltSplice pipeline examines gene-transcript alignments and delineates alternative splice events and splice patterns; this pipeline is extended as AltTrans to delineate isoform transcript patterns for each of which both introns/exons and 'terminating' polyA site are delineated; EST/mRNA sequences that qualify the transcript pattern confirm both the underlying splicing and polyadenylation. The AltPAS pipeline examines gene-transcript alignments and delineates all potential polyA sites irrespective of underlying splicing patterns. Resultant polyA sites from both AltTrans and AltPAS are merged. The generated database reports data on alternative splicing, alternative polyadenylation and the resultant alternate transcript patterns; the basal data is annotated for various biological features. The data (named as integrated AltTrans data) generated for both the organisms of human and mouse is made available through the Alternate Transcript Diversity web site at http://www.ebi.ac.uk/atd/.

conclusionThe reported data set presents alternate transcript patterns that are annotated for both alternative splicing and alternative polyadenylation. Results based on current transcriptome data indicate that the contribution of alternative splicing is larger than that of alternative polyadenylation.

Indexed as

SoftwareAlternative SplicingChromosome MappingDNA Mutational AnalysisGenetic VariationPolyadenylationTranscription FactorsTranscription Factors

Identifiers

PMID16556303
PMCPMC1435940

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.