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Marco Falda

dblp:32/2825 · DBLP profile ↗
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13ranked-venue papers
4as first author
0since 2021 · last 2018
0000-0003-2642-519XORCID · verified

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

Applied, interdisciplinary, general and emerging computing · 7 · 2 first-authorArtificial intelligence and machine learning · 6 · 2 first-authorDatabases, data management, data science and information retrieval · 1

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 7 heaviest of 8, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene expression analysis
differential expression analysis
0.312017
Pathway Inspector: a pathway based web application for RNAseq analysis of model and non-model organisms · Bioinform. 2017
Bioinformatics and computational biology › functional genomics › functional enrichment analysis
pathway enrichment analysis
0.312017
Pathway Inspector: a pathway based web application for RNAseq analysis of model and non-model organisms · Bioinform. 2017
Bioinformatics and computational biology › transcriptomics
RNA-seq analysis
0.312017
Pathway Inspector: a pathway based web application for RNAseq analysis of model and non-model organisms · Bioinform. 2017
Bioinformatics and computational biology › systems bioinformatics › pathway analysis
topology-based pathway analysis
0.312017
Pathway Inspector: a pathway based web application for RNAseq analysis of model and non-model organisms · Bioinform. 2017
Bioinformatics and computational biology
genomics
0.212014
keeSeek: searching distant non-existing words in genomes for PCR-based applications · Bioinform. 2014
Bioinformatics and computational biology › sequence analysis › sequence similarity search
sequence database search
0.212014
keeSeek: searching distant non-existing words in genomes for PCR-based applications · Bioinform. 2014
Bioinformatics and computational biology › genomics
primer design
0.112014
keeSeek: searching distant non-existing words in genomes for PCR-based applications · Bioinform. 2014

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

web application · 0.3GPGPU · 0.2CUDA · 0.2
YearPublicationVenuePosition
2018 Optimizing PCR primers targeting the bacterial 16S ribosomal RNA gene
abstract
BACKGROUND: Targeted amplicon sequencing of the 16S ribosomal RNA gene is one of the key tools for studying microbial diversity. The accuracy of this approach strongly depends on the choice of primer pairs and, in particular, on the balance between efficiency, specificity and sensitivity in the amplification of the different bacterial 16S sequences contained in a sample. There is thus the need for computational methods to design optimal bacterial 16S primers able to take into account the knowledge provided by the new sequencing technologies. RESULTS: We propose here a computational method for optimizing the choice of primer sets, based on multi-objective optimization, which simultaneously: 1) maximizes efficiency and specificity of target amplification; 2) maximizes the number of different bacterial 16S sequences matched by at least one primer; 3) minimizes the differences in the number of primers matching each bacterial 16S sequence. Our algorithm can be applied to any desired amplicon length without affecting computational performance. The source code of the developed algorithm is released as the mopo16S software tool (Multi-Objective Primer Optimization for 16S experiments) under the GNU General Public License and is available at http://sysbiobig.dei.unipd.it/?q=Software#mopo16S . CONCLUSIONS: Results show that our strategy is able to find better primer pairs than the ones available in the literature according to all three optimization criteria. We also experimentally validated three of the primer pairs identified by our method on multiple bacterial species, belonging to different genera and phyla. Results confirm the predicted efficiency and the ability to maximize the number of different bacterial 16S sequences matched by primers.
Francesco Sambo, Francesca Finotello, Enrico Lavezzo, Giacomo Baruzzo, Giulia Masi, Elektra Peta, Marco Falda, Stefano Toppo, Luisa Barzon, Barbara Di Camillo
BMC Bioinform.7
2017 Pathway Inspector: a pathway based web application for RNAseq analysis of model and non-model organisms
abstract
SUMMARY: Pathway Inspector is an easy-to-use web application helping researchers to find patterns of expression in complex RNAseq experiments. The tool combines two standard approaches for RNAseq analysis: the identification of differentially expressed genes and a topology-based analysis of enriched pathways. Pathway Inspector is equipped with ad hoc interactive graphical interfaces simplifying the discovery of modulated pathways and the integration of the differentially expressed genes in the corresponding pathway topology. AVAILABILITY AND IMPLEMENTATION: Pathway Inspector is available at the website http://admiral.fmach.it/PI and has been developed in Python, making use of the Django Web Framework. CONTACT: Contact:[email protected]
Luca Bianco, Samantha Riccadonna, Enrico Lavezzo, Marco Falda, Elide Formentin, Duccio Cavalieri, Stefano Toppo, Paolo Fontana
Bioinform.4
2014 keeSeek: searching distant non-existing words in genomes for PCR-based applications
abstract
UNLABELLED: The search for short words that are absent in the genome of one or more organisms (neverwords, also known as nullomers) is attracting growing interest because of the impact they may have in recent molecular biology applications. keeSeek is able to find absent sequences with primer-like features, which can be used as unique labels for exogenously inserted DNA fragments to recover their exact position into the genome using PCR techniques. The main differences with respect to previously developed tools for neverwords generation are (i) calculation of the distance from the reference genome, in terms of number of mismatches, and selection of the most distant sequences that will have a low probability to anneal unspecifically; (ii) application of a series of filters to discard candidates not suitable to be used as PCR primers. KeeSeek has been implemented in C++ and CUDA (Compute Unified Device Architecture) to work in a General-Purpose Computing on Graphics Processing Units (GPGPU) environment. AVAILABILITY AND IMPLEMENTATION: Freely available under the Q Public License at http://www.medcomp.medicina.unipd.it/main_site/doku.php?id=keeseek.
Marco Falda, Paolo Fontana, Luisa Barzon, Stefano Toppo, Enrico Lavezzo
Bioinform.1
2012 Comparative analysis of algorithms for whole-genome assembly of pyrosequencing data
abstract
Next-generation sequencing technologies have fostered an unprecedented proliferation of high-throughput sequencing projects and a concomitant development of novel algorithms for the assembly of short reads. In this context, an important issue is the need of a careful assessment of the accuracy of the assembly process. Here, we review the efficiency of a panel of assemblers, specifically designed to handle data from GS FLX 454 platform, on three bacterial data sets with different characteristics in terms of reads coverage and repeats content. Our aim is to investigate their strengths and weaknesses in the reconstruction of the reference genomes. In our benchmarking, we assess assemblers' performance, quantifying and characterizing assembly gaps and errors, and evaluating their ability to solve complex genomic regions containing repeats. The final goal of this analysis is to highlight pros and cons of each method, in order to provide the final user with general criteria for the right choice of the appropriate assembly strategy, depending on the specific needs. A further aspect we have explored is the relationship between coverage of a sequencing project and quality of the obtained results. The final outcome suggests that, for a good tradeoff between costs and results, the planned genome coverage of an experiment should not exceed 20-30 ×.
Francesca Finotello, Enrico Lavezzo, Paolo Fontana, Denis Peruzzo, Alessandro Albiero, Luisa Barzon, Marco Falda, Barbara Di Camillo, Stefano Toppo
Briefings Bioinform.7
2012 Argot2: a large scale function prediction tool relying on semantic similarity of weighted Gene Ontology terms
abstract
BACKGROUND: Predicting protein function has become increasingly demanding in the era of next generation sequencing technology. The task to assign a curator-reviewed function to every single sequence is impracticable. Bioinformatics tools, easy to use and able to provide automatic and reliable annotations at a genomic scale, are necessary and urgent. In this scenario, the Gene Ontology has provided the means to standardize the annotation classification with a structured vocabulary which can be easily exploited by computational methods. RESULTS: Argot2 is a web-based function prediction tool able to annotate nucleic or protein sequences from small datasets up to entire genomes. It accepts as input a list of sequences in FASTA format, which are processed using BLAST and HMMER searches vs UniProKB and Pfam databases respectively; these sequences are then annotated with GO terms retrieved from the UniProtKB-GOA database and the terms are weighted using the e-values from BLAST and HMMER. The weighted GO terms are processed according to both their semantic similarity relations described by the Gene Ontology and their associated score. The algorithm is based on the original idea developed in a previous tool called Argot. The entire engine has been completely rewritten to improve both accuracy and computational efficiency, thus allowing for the annotation of complete genomes. CONCLUSIONS: The revised algorithm has been already employed and successfully tested during in-house genome projects of grape and apple, and has proven to have a high precision and recall in all our benchmark conditions. It has also been successfully compared with Blast2GO, one of the methods most commonly employed for sequence annotation. The server is freely accessible at http://www.medcomp.medicina.unipd.it/Argot2.
Marco Falda, Stefano Toppo, Alessandro Pescarolo, Enrico Lavezzo, Barbara Di Camillo, Andrea Facchinetti, Elisa Cilia, Riccardo Velasco, Paolo Fontana
BMC Bioinform.1
2012 SimBioNeT: A Simulator of Biological Network Topology
abstract
Studying biological networks at topological level is a major issue in computational biology studies and simulation is often used in this context, either to assess reverse engineering algorithms or to investigate how topological properties depend on network parameters. In both contexts, it is desirable for a topology simulator to reproduce the current knowledge on biological networks, to be able to generate a number of networks with the same properties and to be flexible with respect to the possibility to mimic networks of different organisms. We propose a biological network topology simulator, SimBioNeT, in which module structures of different type and size are replicated at different level of network organization and interconnected, so to obtain the desired degree distribution, e.g., scale free, and a clustering coefficient constant with the number of nodes in the network, a typical characteristic of biological networks. Empirical assessment of the ability of the simulator to reproduce characteristic properties of biological network and comparison with E. coli and S. cerevisiae transcriptional networks demonstrates the effectiveness of our proposal.
Barbara Di Camillo, Marco Falda, Gianna Toffolo, Claudio Cobelli
IEEE ACM Trans. Comput. Biol. Bioinform.2
2010 Coping with Uncertainty in Temporal Gene Expressions Using Symbolic Representations
Silvana Badaloni, Marco Falda
IPMU (2)2
2009 Fuzzy Mutual Information for Reverse Engineering of Gene Regulatory Networks
Silvana Badaloni, Marco Falda, Paolo Massignan, Francesco Sambo
IJCCI2
2009 Classical and Fuzzy Neighborhood Relations of the Temporal Qualitative Algebra
abstract
In this paper we study the problem of representing different forms of imperfect temporal knowledge. Imperfection in knowledge can be present in the forms of coarse knowledge about temporal events or even in the form of incomplete, imprecise, vague or uncertain temporal information. The two orthogonal notions of coarseness and fuzziness seem to be quite adequate to manage these two kinds of temporal ignorance and they can be combined to develop a more general model. The first part of the present study is dedicated to the definition of a new Neighborhood Temporal Qualitative Algebra nQA starting from Freksa's work about Allen's Algebra neighborhood relations. Freksa's Algebra is merged with the Convex Point Algebra and all the neighborhood relations needed to close the nQA Algebra are computed automatically. The Algebra nQA is tractable. In the second part of the paper, the fuzziness notion is considered and combined with that of conceptual neighborhood. The algebra nQAfuzis defined as a fuzzy extension of the algebra nQA, and the conditions of its tractability are studied.
Silvana Badaloni, Marco Falda
TIME2
2008 Fuzzy conditional temporal problems: Strong and weak consistency
Marco Falda, Francesca Rossi 0001, K. Brent Venable
Eng. Appl. Artif. Intell.1
2007 Computational Complexity Study of Fuzzy Qualitative Temporal Algebra
abstract
Starting from the complexity classification of qualitative algebra recently proposed by Jonsson and Krokhin, we study the tractable fragments of Fuzzy Qualitative AlgebraQAfuz, an integrated framework able to deal with qualitative temporal constraints between points and intervals affected by vagueness and uncertainty. To do this we generalize the results obtained for the classical case exploiting the notion of alpha-cut in relating theQAfuztractable fragments to theirQAclassical counterparts. In order to guarantee the applicability of Path-Consistency algorithm, we prove that the identified fragments are algebras. Besides, we also prove that the set of the identified tractable fuzzy fragments is maximal.
Silvana Badaloni, Marco Falda, Massimiliano Giacomin
FUZZ-IEEE2
2007 Fuzzy Disjunctive Temporal Problems with Classes
abstract
This paper describes a framework for temporal reasoning that allows managing a restricted form of disjunctive temporal constraints without making the modelled problems intractable as in the case of general DTPs. This is obtained by assigning classes to the constraints and by allowing only one constraint per class, in order to build a collection of independent STPs that can share sub-problems and therefore allows increasing algorithm efficiency. The model proposed is directly applied to fuzzy constraint satisfaction problems and can be solved using an extended fuzzy path-consistency algorithm, also presented in the paper. A simple application to medical diagnosis shows its expressive power over previous tractable temporal reasoning models.
Marco Falda
FUZZ-IEEE1
2005 Discriminating Exanthematic Diseases from Temporal Patterns of Patient Symptoms
Silvana Badaloni, Marco Falda
AIME2