Author

Vincenzo Peretti

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genomics· 1

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Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Organism:non-human primate· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Chiara Ferrandi· 1 shared Francesca Ciotola· 1 shared Francesco Strozzi· 1 shared Jared E Decker· 1 shared Jerry F. Taylor· 1 shared Jesse L. HoffiD· 1 shared John L. Williams· 1 shared Luigi Rammuno· 1 shared

Activity by Year

2017-2017 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Chiara Ferrandi

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1 paper

Recent·Most cited

Elucidating the genetic basis of an oligogenic birth defect using whole genome sequence data in a non-model organism, Bubalus bubalis

Lynsey K. Whitacre, Jesse L. Hoff, Robert D. Schnabel, Sara Albarella, Francesca Ciotola, Vincenzo Peretti, Francesco Strozzi, Chiara Ferrandi, Luigi Rammuno, Tad S. Sonstegard, John L. Williams, Jerry F. Taylor, Jared E Decker

This study identifies genetic variants associated with transverse hemimelia in water buffalo using whole genome sequencing and homozygosity mapping, revealing an oligogenic inheritance pattern involving multiple genes.

Scientific Reports · Jan 3, 2017Peer-reviewedGenomics