Demo Data from SIGIR 2026 / reviewers in the wild / expert
Paolo Uva
dblp:62/7104
· DBLP profile ↗
3ranked-venue papers
1as first author
1since 2021 · last 2021
0000-0002-9524-8492ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 3 · 1 first-author · 1 since 2021
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
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 4 heaviest of 4, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology
metagenomics |
0.2 | 1 | 2014 | Orione, a web-based framework for NGS analysis in microbiology · Bioinform. 2014 |
Bioinformatics and computational biology › genomics
next-generation sequencing data analysis |
0.2 | 1 | 2014 | Orione, a web-based framework for NGS analysis in microbiology · Bioinform. 2014 |
Bioinformatics and computational biology › genomics › microbial genomics
bacterial genomics |
0.1 | 1 | 2014 | Orione, a web-based framework for NGS analysis in microbiology · Bioinform. 2014 |
Bioinformatics and computational biology
microbiology |
0.1 | 1 | 2014 | Orione, a web-based framework for NGS analysis in microbiology · Bioinform. 2014 |
Methods — techniques the papers use, named apart from their topics
galaxy workflow · 0.2
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2021 | Laniakea@ReCaS: exploring the potential of customisable Galaxy on-demand instances as a cloud-based serviceabstractBACKGROUND: Improving the availability and usability of data and analytical tools is a critical precondition for further advancing modern biological and biomedical research. For instance, one of the many ramifications of the COVID-19 global pandemic has been to make even more evident the importance of having bioinformatics tools and data readily actionable by researchers through convenient access points and supported by adequate IT infrastructures. One of the most successful efforts in improving the availability and usability of bioinformatics tools and data is represented by the Galaxy workflow manager and its thriving community. In 2020 we introduced Laniakea, a software platform conceived to streamline the configuration and deployment of "on-demand" Galaxy instances over the cloud. By facilitating the set-up and configuration of Galaxy web servers, Laniakea provides researchers with a powerful and highly customisable platform for executing complex bioinformatics analyses. The system can be accessed through a dedicated and user-friendly web interface that allows the Galaxy web server's initial configuration and deployment. RESULTS: "Laniakea@ReCaS", the first instance of a Laniakea-based service, is managed by ELIXIR-IT and was officially launched in February 2020, after about one year of development and testing that involved several users. Researchers can request access to Laniakea@ReCaS through an open-ended call for use-cases. Ten project proposals have been accepted since then, totalling 18 Galaxy on-demand virtual servers that employ ~ 100 CPUs, ~ 250 GB of RAM and ~ 5 TB of storage and serve several different communities and purposes. Herein, we present eight use cases demonstrating the versatility of the platform. CONCLUSIONS: During this first year of activity, the Laniakea-based service emerged as a flexible platform that facilitated the rapid development of bioinformatics tools, the efficient delivery of training activities, and the provision of public bioinformatics services in different settings, including food safety and clinical research. Laniakea@ReCaS provides a proof of concept of how enabling access to appropriate, reliable IT resources and ready-to-use bioinformatics tools can considerably streamline researchers' work. Marco Antonio Tangaro, Pietro Mandreoli, Matteo Chiara, Giacinto Donvito, Marica Antonacci, Antonio Parisi, Angelica Bianco, Angelo Romano, Daniela Manila Bianchi, Davide Cangelosi, Paolo Uva, Ivan Molineris, Vladimir Nosi, Raffaele A. Calogero, Luca Alessandrì, Elena Pedrini, Marina Mordenti, Emanuele Bonetti, Luca Sangiorgi, Graziano Pesole, Federico Zambelli |
BMC Bioinform. | 11 |
| 2014 | Orione, a web-based framework for NGS analysis in microbiologyabstractUNLABELLED: End-to-end next-generation sequencing microbiology data analysis requires a diversity of tools covering bacterial resequencing, de novo assembly, scaffolding, bacterial RNA-Seq, gene annotation and metagenomics. However, the construction of computational pipelines that use different software packages is difficult owing to a lack of interoperability, reproducibility and transparency. To overcome these limitations we present Orione, a Galaxy-based framework consisting of publicly available research software and specifically designed pipelines to build complex, reproducible workflows for next-generation sequencing microbiology data analysis. Enabling microbiology researchers to conduct their own custom analysis and data manipulation without software installation or programming, Orione provides new opportunities for data-intensive computational analyses in microbiology and metagenomics. AVAILABILITY AND IMPLEMENTATION: Orione is available online at http://orione.crs4.it. Gianmauro Cuccuru, Massimiliano Orsini, Andrea Pinna 0003, Andrea Sbardellati, Nicola Soranzo, Antonella Travaglione, Paolo Uva, Gianluigi Zanetti, Giorgio Fotia |
Bioinform. | 7 |
| 2008 | CrossHybDetector: detection of cross-hybridization events in DNA microarray experimentsabstractBACKGROUND: DNA microarrays contain thousands of different probe sequences represented on their surface. These are designed in such a way that potential cross-hybridization reactions with non-target sequences are minimized. However, given the large number of probes, the occurrence of cross hybridization events cannot be excluded. This problem can dramatically affect the data quality and cause false positive/false negative results. RESULTS: CrossHybDetector is a software package aimed at the identification of cross-hybridization events occurred during individual array hybridization, by using the probe sequences and the array intensity values. As output, the software provides the user with a list of array spots potentially 'corrupted' and their associated p-values calculated by Monte Carlo simulations. Graphical plots are also generated, which provide a visual and global overview of the quality of the microarray experiment with respect to cross-hybridization issues. CONCLUSION: CrossHybDetector is implemented as a package for the statistical computing environment R and is freely available under the LGPL license within the CRAN project. Paolo Uva, Emanuele de Rinaldis |
BMC Bioinform. | 1 |