Author

Barbara Gega

University of FlorenceORCID 0000-0002-5797-3546Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:long-read sequencing· 1 Research Focus:software / tool· 1 Approach:statistical model· 1

Frequent Co-Authors

Alberto MagiiD· 2 shared Alessandra MingrinoiD· 2 shared Gianluca MatteiiD· 2 shared Davide BologniniiD· 1 shared Francesco De LoguiD· 1 shared Gianmaria FrigèiD· 1 shared Laura DesiderioiD· 1 shared Luca MazzarellaiD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersBioinformatics

Alberto MagiORCID

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2 papers

Recent·Most cited

PoreMeth2: decoding the evolution of methylome alterations with Nanopore sequencing

Gianluca Mattei, Marta Baragli, Barbara Gega, Alessandra Mingrino, Martina Chieca, Tommaso Ducci, Gianmaria Frigè, Luca Mazzarella, Romina D’Aurizio, Francesco De Logu, Romina Nassini, Pier Giuseppe Pelicci, Alberto Magi

PoreMeth2 identifies differentially methylated regions using Nanopore sequencing, revealing epigenomic changes in cancer and glial cells.

bioRxiv · Oct 3, 2024 · PreprintBioinformatics

Third Generation Cytogenetic Analysis (TGCA): diagnostic application of long-read sequencing.

Pamela Magini, Alessandra Mingrino, Barbara Gega, Gianluca Mattei, Roberto Semeraro, Davide Bolognini, Patrizia Mongelli, Laura Desiderio, Maria Carla Pittalis, Tommaso Pippucci, Alberto Magi

This study demonstrates that long-read sequencing using Oxford Nanopore Technologies can rapidly and accurately detect pathogenic unbalanced structural variants with resolution comparable to traditional methods.

Journal of Molecular Diagnostics · May 5, 2022Peer-reviewedGenomics