Author

Barbara Iadarola

University of VeronaORCID 0000-0002-8173-3200Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Organism:human· 1

Frequent Co-Authors

Cristina Beltrami· 2 shared Denise LavezzariiD· 2 shared Marzia RossatoiD· 2 shared Massimo DelledonneiD· 2 shared Alessandra ModiiD· 1 shared Alessandro SalviatiiD· 1 shared Annalisa VetroiD· 1 shared Chiara Degli Esposti· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Cristina Beltrami

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2 papers

Recent·Most cited

Whole-exome sequencing of the mummified remains of Cangrande della Scala (1291-1329 CE) indicates the first known case of late-onset Pompe disease

Barbara Iadarola, Denise Lavezzari, Alessandra Modi, Chiara Degli Esposti, Cristina Beltrami, Marzia Rossato, Valentina Zaro, Ettore Napione, Leonardo Latella, Martina Lari, David Caramelli, Alessandro Salviati, Massimo Delledonne

The paper performs whole-exome sequencing on mummified remains to identify a genetic mutation associated with late-onset Pompe disease in a historical figure.

Scientific Reports · Oct 26, 2021Peer-reviewedGenetic & Genomic Medicine

Enhanced targeted resequencing by optimizing the combination of enrichment technology and DNA fragment length

Barbara Iadarola, Luciano Xumerle, Denise Lavezzari, Marta Paterno, Luca Marcolungo, Cristina Beltrami, Elisabetta Fortunati, Davide Mei, Annalisa Vetro, Renzo Guerrini, Elena Parrini, Marzia Rossato, Massimo Delledonne

The paper evaluates how DNA fragment length and enrichment technology affect genotypability in whole-exome sequencing, finding that longer fragments improve callable bases and genotypability across different platforms.

Scientific Reports · Jun 10, 2020Peer-reviewedGenomics