TY - JOUR
T1 - ASPicDB
T2 - A database of annotated transcript and protein variants generated by alternative splicing
AU - Martelli, Pier L.
AU - D'Antonio, Mattia
AU - Bonizzoni, Paola
AU - Castrignanò, Tiziana
AU - D'Erchia, Anna M.
AU - De Meo, Paolo D.Onorio
AU - Fariselli, Piero
AU - Finelli, Michele
AU - Licciulli, Flavio
AU - Mangiulli, Marina
AU - Mignone, Flavio
AU - Pavesi, Giulio
AU - Picardi, Ernesto
AU - Rizzi, Raffaella
AU - Rossi, Ivan
AU - Valletti, Alessio
AU - Zauli, Andrea
AU - Zambelli, Federico
AU - Casadio, Rita
AU - Pesole, Graziano
N1 - Funding Information:
Ministero dell’Istruzione, dell’Università e della Ricerca: Fondo Italiano Ricerca di Base: ‘Laboratorio Internazionale di Bioinformatica’ (LIBI); Laboratorio di Bioinformatica per la Biodiversità Molecolare (MBLAB) and Telethon (project GGP01658). Funding for open access charge: Ministero dell’Università e della Ricerca: Fondo Italiano Ricerca di Base: ‘Laboratorio Internazionale di Bioinformatica’ (LIBI).
PY - 2011/1
Y1 - 2011/1
N2 - Alternative splicing is emerging as a major mechanism for the expansion of the transcriptome and proteome diversity, particularly in human and other vertebrates. However, the proportion of alternative transcripts and proteins actually endowed with functional activity is currently highly debated. We present here a new release of ASPicDB which now provides a unique annotation resource of human protein variants generated by alternative splicing. A total of 256 939 protein variants from 17 191 multi-exon genes have been extensively annotated through state of the art machine learning tools providing information of the protein type (globular and transmembrane), localization, presence of PFAM domains, signal peptides, GPIanchor propeptides, transmembrane and coiledcoil segments. Furthermore, full-length variants can be now specifically selected based on the annotation of CAGE-tags and polyA signal and/or polyA sites, marking transcription initiation and termination sites, respectively. The retrieval can be carried out at gene, transcript, exon, protein or splice site level allowing the selection of data sets fulfilling one or more features settled by the user. The retrieval interface also enables the selection of protein variants showing specific differences in the annotated features. ASPicDB is available at http://www .caspur.it/ASPicDB/.
AB - Alternative splicing is emerging as a major mechanism for the expansion of the transcriptome and proteome diversity, particularly in human and other vertebrates. However, the proportion of alternative transcripts and proteins actually endowed with functional activity is currently highly debated. We present here a new release of ASPicDB which now provides a unique annotation resource of human protein variants generated by alternative splicing. A total of 256 939 protein variants from 17 191 multi-exon genes have been extensively annotated through state of the art machine learning tools providing information of the protein type (globular and transmembrane), localization, presence of PFAM domains, signal peptides, GPIanchor propeptides, transmembrane and coiledcoil segments. Furthermore, full-length variants can be now specifically selected based on the annotation of CAGE-tags and polyA signal and/or polyA sites, marking transcription initiation and termination sites, respectively. The retrieval can be carried out at gene, transcript, exon, protein or splice site level allowing the selection of data sets fulfilling one or more features settled by the user. The retrieval interface also enables the selection of protein variants showing specific differences in the annotated features. ASPicDB is available at http://www .caspur.it/ASPicDB/.
UR - http://www.scopus.com/inward/record.url?scp=78651298898&partnerID=8YFLogxK
U2 - 10.1093/nar/gkq1073
DO - 10.1093/nar/gkq1073
M3 - Article
SN - 0305-1048
VL - 39
SP - D80-D85
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - SUPPL. 1
ER -