Graziano Pesole

Orcid: 0000-0003-3663-0859

According to our database1, Graziano Pesole authored at least 93 papers between 1993 and 2023.

Collaborative distances:
  • Dijkstra number2 of five.
  • Erdős number3 of four.

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
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Links

Online presence:

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Bibliography

2023
UTRdb 2.0: a comprehensive, expert curated catalog of eukaryotic mRNAs untranslated regions.
Nucleic Acids Res., January, 2023

2022
MetaCOXI: an integrated collection of metazoan mitochondrial cytochrome oxidase subunit-I DNA sequences.
Database J. Biol. Databases Curation, 2022

The Laniakea Dashboard and Storage Encryption Components: A Foundation for Developing On-Demand Cloud Services for Life Science.
Proceedings of the Current Trends in Web Engineering, 2022

2021
ITSoneWB: profiling global taxonomic diversity of eukaryotic communities on Galaxy.
Bioinform., November, 2021

REDIportal: millions of novel A-to-I RNA editing events from thousands of RNAseq experiments.
Nucleic Acids Res., 2021

Recommendations for connecting molecular sequence and biodiversity research infrastructures through ELIXIR.
F1000Research, 2021

Laniakea@ReCaS: exploring the potential of customisable Galaxy on-demand instances as a cloud-based service.
BMC Bioinform., 2021

CorGAT: a tool for the functional annotation of SARS-CoV-2 genomes.
Bioinform., 2021

VINYL: Variant prIoritizatioN bY survivaL analysis.
Bioinform., 2021

Next generation sequencing of SARS-CoV-2 genomes: challenges, applications and opportunities.
Briefings Bioinform., 2021

2020
HPC-REDItools: a novel HPC-aware tool for improved large scale RNA-editing analysis.
BMC Bioinform., 2020

ELIXIR-IT HPC@CINECA: high performance computing resources for the bioinformatics community.
BMC Bioinform., 2020

Critical assessment of bioinformatics methods for the characterization of pathological repeat expansions with single-molecule sequencing data.
Briefings Bioinform., 2020

2019
Elucidating the editome: bioinformatics approaches for RNA editing detection.
Briefings Bioinform., 2019

2018
ITSoneDB: a comprehensive collection of eukaryotic ribosomal RNA Internal Transcribed Spacer 1 (ITS1) sequences.
Nucleic Acids Res., 2018

Unbiased Taxonomic Annotation of Metagenomic Samples.
J. Comput. Biol., 2018

2017
REDIportal: a comprehensive database of A-to-I RNA editing events in humans.
Nucleic Acids Res., 2017

MetaShot: an accurate workflow for taxon classification of host-associated microbiome from shotgun metagenomic data.
Bioinform., 2017

2015
BioMaS: a modular pipeline for Bioinformatic analysis of Metagenomic AmpliconS.
BMC Bioinform., 2015

MSA-PAD: DNA multiple sequence alignment framework based on PFAM accessed domain information.
Bioinform., 2015

2014
EasyCluster2: an improved tool for clustering and assembling long transcriptome reads.
BMC Bioinform., 2014

MToolBox: a highly automated pipeline for heteroplasmy annotation and prioritization analysis of human mitochondrial variants in high-throughput sequencing.
Bioinform., 2014

ODESSA: A high performance analysis pipeline for Ultra Deep targeted Exome Sequencing data.
Proceedings of the International Conference on High Performance Computing & Simulation, 2014

2013
PscanChIP: finding over-represented transcription factor-binding site motifs and their correlations in sequences from ChIP-Seq experiments.
Nucleic Acids Res., 2013

SpliceAid-F: a database of human splicing factors and their RNA-binding sites.
Nucleic Acids Res., 2013

WEP: a high-performance analysis pipeline for whole-exome data.
BMC Bioinform., 2013

NGS-Trex: Next Generation Sequencing Transcriptome profile explorer.
BMC Bioinform., 2013

REDItools: high-throughput RNA editing detection made easy.
Bioinform., 2013

Motif discovery and transcription factor binding sites before and after the next-generation sequencing era.
Briefings Bioinform., 2013

Clustering and Assembling Large Transcriptome Datasets by EasyCluster2.
Proceedings of the Emerging Intelligent Computing Technology and Applications, 2013

2012
Cscan: finding common regulators of a set of genes by using a collection of genome-wide ChIP-seq datasets.
Nucleic Acids Res., 2012

MitoZoa 2.0: a database resource and search tools for comparative and evolutionary analyses of mitochondrial genomes in Metazoa.
Nucleic Acids Res., 2012

PIntron: a fast method for detecting the gene structure due to alternative splicing via maximal pairings of a pattern and a text.
BMC Bioinform., 2012

Editorial.
Briefings Bioinform., 2012

Reference databases for taxonomic assignment in metagenomics.
Briefings Bioinform., 2012

2011
ASPicDB: a database of annotated transcript and protein variants generated by alternative splicing.
Nucleic Acids Res., 2011

ExpEdit: a webserver to explore human RNA editing in RNA-Seq experiments.
Bioinform., 2011

2010
UTRdb and UTRsite (RELEASE 2010): a collection of sequences and regulatory motifs of the untranslated regions of eukaryotic mRNAs.
Nucleic Acids Res., 2010

Bioinformatics approaches for genomics and post genomics applications of next-generation sequencing.
Briefings Bioinform., 2010

New Tools for Expression Alternative Splicing Validation.
Proceedings of the Advanced Intelligent Computing Theories and Applications, 2010

2009
Pscan: finding over-represented transcription factor binding site motifs in sequences from co-regulated or co-expressed genes.
Nucleic Acids Res., 2009

Detecting Alternative Gene Structures from Spliced ESTs: A Computational Approach.
J. Comput. Biol., 2009

Accurate discrimination of conserved coding and non-coding regions through multiple indicators of evolutionary dynamics.
BMC Bioinform., 2009

EasyCluster: a fast and efficient gene-oriented clustering tool for large-scale transcriptome data.
BMC Bioinform., 2009

Statistical assessment of discriminative features for protein-coding and non coding cross-species conserved sequence elements.
BMC Bioinform., 2009

2008
Bioinformatics in Italy: BITS2007, the fourth annual meeting of the Italian Society of Bioinformatics.
BMC Bioinform., 2008

ASPicDB: A database resource for alternative splicing analysis.
Bioinform., 2008

Correlated substitution analysis and the prediction of amino acid structural contacts.
Briefings Bioinform., 2008

HT-RLS: High-Throughput Web Tool for Analysis of DNA Microarray Data Using RLS classifiers.
Proceedings of the 8th IEEE International Symposium on Cluster Computing and the Grid (CCGrid 2008), 2008

GenePC and ASPIC Integrate Gene Predictions with Expressed Sequence Alignments To Predict Alternative Transcripts.
Proceedings of the 6th Asia-Pacific Bioinformatics Conference, 2008

2007
A high performance grid-web service framework for the identification of 'conserved sequence tags'.
Future Gener. Comput. Syst., 2007

p53FamTaG: a database resource of human p53, p63 and p73 direct target genes combining <i>in silico </i>prediction and microarray data.
BMC Bioinform., 2007

WeederH: an algorithm for finding conserved regulatory motifs and regions in homologous sequences.
BMC Bioinform., 2007

Bioinformatics in Italy: BITS2006, the third annual meeting of the Italian Society of Bioinformatics.
BMC Bioinform., 2007

Statistical assessment of functional categories of genes deregulated in pathological conditions by using microarray data.
Bioinform., 2007

Selection of relevant genes in cancer diagnosis based on their prediction accuracy.
Artif. Intell. Medicine, 2007

2006
MoD Tools: regulatory motif discovery in nucleotide sequences from co-regulated or homologous genes.
Nucleic Acids Res., 2006

ASPIC: a web resource for alternative splicing prediction and transcript isoforms characterization.
Nucleic Acids Res., 2006

On the statistical assessment of classifiers using DNA microarray data.
BMC Bioinform., 2006

GenoMiner: a tool for genome-wide search of coding and non-coding conserved sequence tags.
Bioinform., 2006

Classification error as a measure of gene relevance in cancer diagnosis.
Proceedings of the International Joint Conference on Neural Networks, 2006

2005
UTRdb and UTRsite: a collection of sequences and regulatory motifs of the untranslated regions of eukaryotic mRNAs.
Nucleic Acids Res., 2005

DG-CST (Disease Gene Conserved Sequence Tags), a database of human-mouse conserved elements associated to disease genes.
Nucleic Acids Res., 2005

Overview of BITS2005, the Second Annual Meeting of the Italian Bioinformatics Society.
BMC Bioinform., 2005

ASPIC: a novel method to predict the exon-intron structure of a gene that is optimally compatible to a set of transcript sequences.
BMC Bioinform., 2005

Regularized Least Squares Cancer Classifiers from DNA microarray data.
BMC Bioinform., 2005

SVM and RLS Models for Cancer Classification.
Proceedings of the IASTED International Conference on Computational Intelligence, 2005

2004
Weeder Web: discovery of transcription factor binding sites in a set of sequences from co-regulated genes.
Nucleic Acids Res., 2004

CSTminer: a web tool for the identification of coding and noncoding conserved sequence tags through cross-species genome comparison.
Nucleic Acids Res., 2004

An Algorithm for Finding Conserved Secondary Structure Motifs in Unaligned RNA Sequences.
J. Comput. Sci. Technol., 2004

WebVar: a resource for the rapid estimation of relative site variability from multiple sequence alignments.
Bioinform., 2004

DNAfan: a software tool for automated extraction and analysis of user-defined sequence regions.
Bioinform., 2004

In silico representation and discovery of transcription factor binding sites.
Briefings Bioinform., 2004

2003
PatSearch: a program for the detection of patterns and structural motifs in nucleotide sequences.
Nucleic Acids Res., 2003

The estimation of relative site variability among aligned homologous protein sequences.
Bioinform., 2003

A Method to Detect Gene Structure and Alternative Splice Sites by Agreeing ESTs to a Genomic Sequence.
Proceedings of the Algorithms in Bioinformatics, Third International Workshop, 2003

Predicting Conserved Hairpin Motifs in Unaligned RNA Sequences.
Proceedings of the 15th IEEE International Conference on Tools with Artificial Intelligence (ICTAI 2003), 2003

Handbook of Comparative Genomics - Principles and Methodology.
Wiley, ISBN: 978-0-471-39128-9, 2003

2002
UTRdb and UTRsite: specialized databases of sequences and functional elements of 5' and 3' untranslated regions of eukaryotic mRNAs. Update 2002.
Nucleic Acids Res., 2002

MitoNuc: a database of nuclear genes coding for mitochondrial proteins. Update 2002.
Nucleic Acids Res., 2002

Evolutionary Dynamics of Mammalian MRNA Untranslated Regions by Comparative Analysis of Orthologous Human, Artiodactyl and Rodent Gene Pairs.
Comput. Chem., 2002

2001
Methods for Pattern Discovery in Unaligned Biological Sequences.
Briefings Bioinform., 2001

An algorithm for finding signals of unknown length in DNA sequences.
Proceedings of the Ninth International Conference on Intelligent Systems for Molecular Biology, 2001

2000
UTRdb and UTRsite: specialized databases of sequences and functional elements of 5' and 3' untranslated regions of eukaryotic mRNAs.
Nucleic Acids Res., 2000

MitoNuc and MitoAln: two related databases of nuclear genes coding for mitochondrial proteins.
Nucleic Acids Res., 2000

PatSearch: a pattern matcher software that finds functional elements in nucleotide and protein sequences and assesses their statistical significance.
Bioinform., 2000

The Untranslated Regions of Eukaryotic MRNAs: Structure, Function, Evolution and Bioinformatic Tools for Their Analysis.
Briefings Bioinform., 2000

1999
UTRdb: a specialized database of 5' and 3' untranslated regions of eukaryotic mRNAs.
Nucleic Acids Res., 1999

1998
UTRdb: a specialized database of 5'- and 3'-untranslated regions of eukaryotic mRNAs.
Nucleic Acids Res., 1998

1996
Databases of MRNA Untranslated Regions for Metazoa.
Comput. Chem., 1996

CLEANUP: a fast computer program for removing redundancies from nucleotide sequence databases.
Comput. Appl. Biosci., 1996

1993
FASTPAT: a fast and efficient algorithm for string searching in DNA sequences.
Comput. Appl. Biosci., 1993

SIMD parallelization of the WORDUP algorithm for detecting statistically significant patterns in DNA sequences.
Comput. Appl. Biosci., 1993


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