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Alberto Magi

Showing results (21-30 of 83) with videos related to

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Plos One|July 5, 2012
WNP: a novel algorithm for gene products annotation from weighted functional networksAlberto Magi, Lorenzo Tattini, Matteo Benelli, et al.
Nucleic Acids Research|August 11, 2016
Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2Romina D'Aurizio, Tommaso Pippucci, Lorenzo Tattini, et al.
Biostatistics (Oxford, England)|December 2, 2009
A shifting level model algorithm that identifies aberrations in array-CGH dataAlberto Magi, Matteo Benelli, Giuseppina Marseglia, et al.
Molecular Oncology|May 26, 2025
Landscape of BRAF transcript variants in human cancerMaurizio S Podda, Danilo Tatoni, Gianluca Mattei, et al.
Frontiers in Physiology|September 9, 2017
Genetic Bases of Bicuspid Aortic Valve: The Contribution of Traditional and High-Throughput Sequencing Approaches on Research and DiagnosisBetti Giusti, Elena Sticchi, Rosina De Cario, et al.
Bioinformatics (Oxford, England)|October 8, 2019
VISOR: a versatile haplotype-aware structural variant simulator for short- and long-read sequencingDavide Bolognini, Ashley Sanders, Jan O Korbel, et al.
Genes|April 9, 2014
Bioinformatics for next generation sequencing dataAlberto Magi, Matteo Benelli, Alessia Gozzini, et al.
Free Radical Research|May 12, 2012
Genetic polymorphisms of antioxidant enzymes as risk factors for oxidative stress-associated complications in preterm infantsBetti Giusti, Anna Vestrini, Chiara Poggi, et al.
Computational and Structural Biotechnology Journal|August 11, 2020
AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomicsAlberto Magi, Tania Giangregorio, Roberto Semeraro, et al.
Clinical Chemistry|October 25, 2019
Long Reads, Short Time: Feasibility of Prenatal Sample Karyotyping by Nanopore Genome SequencingNiccolò Bartalucci, Simone Romagnoli, Elisa Contini, et al.
Pageof 9

Showing results (21-30 of 83) with videos related to

Sort By:
Pageof 9
Plos One|July 5, 2012
WNP: a novel algorithm for gene products annotation from weighted functional networksAlberto Magi, Lorenzo Tattini, Matteo Benelli, et al.
Nucleic Acids Research|August 11, 2016
Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2Romina D'Aurizio, Tommaso Pippucci, Lorenzo Tattini, et al.
Biostatistics (Oxford, England)|December 2, 2009
A shifting level model algorithm that identifies aberrations in array-CGH dataAlberto Magi, Matteo Benelli, Giuseppina Marseglia, et al.
Molecular Oncology|May 26, 2025
Landscape of BRAF transcript variants in human cancerMaurizio S Podda, Danilo Tatoni, Gianluca Mattei, et al.
Frontiers in Physiology|September 9, 2017
Genetic Bases of Bicuspid Aortic Valve: The Contribution of Traditional and High-Throughput Sequencing Approaches on Research and DiagnosisBetti Giusti, Elena Sticchi, Rosina De Cario, et al.
Bioinformatics (Oxford, England)|October 8, 2019
VISOR: a versatile haplotype-aware structural variant simulator for short- and long-read sequencingDavide Bolognini, Ashley Sanders, Jan O Korbel, et al.
Genes|April 9, 2014
Bioinformatics for next generation sequencing dataAlberto Magi, Matteo Benelli, Alessia Gozzini, et al.
Free Radical Research|May 12, 2012
Genetic polymorphisms of antioxidant enzymes as risk factors for oxidative stress-associated complications in preterm infantsBetti Giusti, Anna Vestrini, Chiara Poggi, et al.
Computational and Structural Biotechnology Journal|August 11, 2020
AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomicsAlberto Magi, Tania Giangregorio, Roberto Semeraro, et al.
Clinical Chemistry|October 25, 2019
Long Reads, Short Time: Feasibility of Prenatal Sample Karyotyping by Nanopore Genome SequencingNiccolò Bartalucci, Simone Romagnoli, Elisa Contini, et al.
Pageof 9