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Erik Dassi

dblp:85/10673 · DBLP profile ↗
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2ranked-venue papers
1as first author
0since 2021 · last 2014
0000-0003-4487-0449ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
2 papers
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
multi-omics data integration
0.212014
tRanslatome: an R/Bioconductor package to portray translational control · Bioinform. 2014
Bioinformatics and computational biology › gene regulation › post-transcriptional regulation
translational control analysis
0.212014
tRanslatome: an R/Bioconductor package to portray translational control · Bioinform. 2014
Bioinformatics and computational biology › biological database
biological database curation
0.012012
AURA: Atlas of UTR Regulatory Activity · Bioinform. 2012

Methods — techniques the papers use, named apart from their topics

enrichment analysis · 0.2differential expression analysis · 0.2
YearPublicationVenuePosition
2014 tRanslatome: an R/Bioconductor package to portray translational control
abstract
UNLABELLED: High-throughput technologies have led to an explosion of genomic data available for automated analysis. The consequent possibility to simultaneously sample multiple layers of variation along the gene expression flow requires computational methods integrating raw information from different '-omics'. It has been recently demonstrated that translational control is a widespread phenomenon, with profound and still underestimated regulation capabilities. Although detecting changes in the levels of total messenger RNAs (mRNAs; the transcriptome), of polysomally loaded mRNAs (the translatome) and of proteins (the proteome) is experimentally feasible in a high-throughput way, the integration of these levels is still far from being robustly approached. Here we introduce tRanslatome, a new R/Bioconductor package, which is a complete platform for the simultaneous pairwise analysis of transcriptome, translatome and proteome data. The package includes most of the available statistical methods developed for the analysis of high-throughput data, allowing the parallel comparison of differentially expressed genes and the corresponding differentially enriched biological themes. Notably, it also enables the prediction of translational regulatory elements on mRNA sequences. The utility of this tool is demonstrated with two case studies. AVAILABILITY AND IMPLEMENTATION: tRanslatome is available in Bioconductor.
Toma Tebaldi, Erik Dassi, Galena Pisoni, Gabriella Viero, Alessandro Quattrone
Bioinform.2
2012 AURA: Atlas of UTR Regulatory Activity
abstract
SUMMARY: The Atlas of UTR Regulatory Activity (AURA) is a manually curated and comprehensive catalog of human mRNA untranslated regions (UTRs) and UTR regulatory annotations. Through its intuitive web interface, it provides full access to a wealth of information on UTRs that integrates phylogenetic conservation, RNA sequence and structure data, single nucleotide variation, gene expression and gene functional descriptions from literature and specialized databases. AVAILABILITY: http://aura.science.unitn.it CONTACT: [email protected]; [email protected] SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Erik Dassi, A. Malossini, Angela Re, Tommaso Mazza, Toma Tebaldi, Luigi Caputi, Alessandro Quattrone
Bioinform.1