EDBT 2026 Demo / reviewers in the wild / expert
Bruno Samorì
dblp:67/2411
· DBLP profile ↗
2ranked-venue papers
0as first author
0since 2021 · last 2011
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2
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
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › RNA biology › RNA analysis › RNA bioinformatics
RNA folding kinetics |
0.1 | 1 | 2011 | Open source platform for the execution and analysis of mechanical refolding experiments · Bioinform. 2011 |
Bioinformatics and computational biology
single-molecule force spectroscopy |
0.1 | 1 | 2011 | Open source platform for the execution and analysis of mechanical refolding experiments · Bioinform. 2011 |
Bioinformatics and computational biology
single-molecule analysis |
0.0 | 1 | 2009 | Hooke: an open software platform for force spectroscopy · Bioinform. 2009 |
Methods — techniques the papers use, named apart from their topics
kinetic modeling · 0.1force spectroscopy analysis · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2011 | Open source platform for the execution and analysis of mechanical refolding experimentsabstractMOTIVATION: Single-molecule force spectroscopy has facilitated the experimental investigation of biomolecular force-coupled kinetics, from which the kinetics at zero force can be extrapolated via explicit theoretical models. The atomic force microscope (AFM) in particular is routinely used to study protein unfolding kinetics, but only rarely protein folding kinetics. The discrepancy arises because mechanical protein refolding studies are more technically challenging. RESULTS: We developed software that can drive and analyse mechanical refolding experiments when used with the commercial AFM setup 'Picoforce AFM', Bruker (previously Digital Instruments). We expect the software to be easily adaptable to other AFM setups. We also developed an improved method for the statistical characterization of protein folding kinetics, and implemented it into an AFM-independent software module. AVAILABILITY: Software and documentation are available at http://code.google.com/p/refolding under Apache License 2.0. Daniel Aioanei, Marco Brucale, Bruno Samorì |
Bioinform. | 3 |
| 2009 | Hooke: an open software platform for force spectroscopyabstractSUMMARY: Hooke is an open source, extensible software intended for analysis of atomic force microscope (AFM)-based single molecule force spectroscopy (SMFS) data. We propose it as a platform on which published and new algorithms for SMFS analysis can be integrated in a standard, open fashion, as a general solution to the current lack of a standard software for SMFS data analysis. Specific features and support for file formats are coded as independent plugins. Any user can code new plugins, extending the software capabilities. Basic automated dataset filtering and semi-automatic analysis facilities are included. AVAILABILITY: Software and documentation are available at (http://code.google.com/p/hooke). Hooke is a free software under the GNU Lesser General Public License. Massimo Sandal, Fabrizio Benedetti, Marco Brucale, Alberto Gomez-Casado, Bruno Samorì |
Bioinform. | 5 |