Federico A. Santoni

According to our database, Federico A. Santoni authored at least 7 papers between 2005 and 2025.

Collaborative distances:

• Dijkstra number of five.
• Erdős number of four.

2025

GenMasterTable: a user-friendly desktop application for filtering, summarising, and visualising large-scale annotated genetic variants.

Jing Zhai, Nelly Pitteloud, Federico A. Santoni

BMC Bioinform., December, 2025

2024

pyTWMR: transcriptome-wide Mendelian randomization in python.

Sergey Oreshkov, Kaido Lepik, Federico A. Santoni

Bioinform., 2024

2022

CoverageMaster: comprehensive CNV detection and visualization from NGS short reads for genetic medicine applications.

Melivoia Rapti, Yassine Zouaghi, Jenny Meylan, Emmanuelle Ranza, Stylianos E. Antonarakis, Federico Andrea Santoni

Briefings Bioinform., 2022

2015

CATCHing putative causative variants in consanguineous families.

Federico Andrea Santoni, Periklis Makrythanasis, Stylianos E. Antonarakis

BMC Bioinform., 2015

2010

Deciphering the Code for Retroviral Integration Target Site Selection.

Federico Andrea Santoni, Oliver Hartley, Jeremy Luban

PLoS Comput. Biol., 2010

2009

Biodoop: Bioinformatics on Hadoop.

Simone Leo, Federico Andrea Santoni, Gianluigi Zanetti

Proceedings of the ICPPW 2009, 2009

2005

AntiHunter 2.0: increased speed and sensitivity in searching BLAST output for EST antisense transcripts.

Giovanni Lavorgna, Riccardo Triunfo, Federico Andrea Santoni, Ugo Orfanelli, Sara Noci, Alessandro Bulfone, Gianluigi Zanetti, Giorgio Casari

Nucleic Acids Res., 2005