Evaluation of Germline Structural Variant Calling Methods for Nanopore Sequencing Data

por Bolognini , Davide, Magi , Alberto
Publicado 2021

Editorial: Repetitive Structures in Biological Sequences: Algorithms and Applications

por Pellegrini, Marco, Magi, Alberto, Iliopoulos, Costas S.
Publicado 2016

XCAVATOR: accurate detection and genotyping of copy number variants from second and third generation whole-genome sequencing experiments

por Magi, Alberto, Pippucci, Tommaso, Sidore, Carlo
Publicado 2017

Xome-Blender: A novel cancer genome simulator

por Semeraro, Roberto, Orlandini, Valerio, Magi, Alberto
Publicado 2018

Versatile Quality Control Methods for Nanopore Sequencing

por Bolognini, Davide, Semeraro, Roberto, Magi, Alberto
Publicado 2019

From multitude to singularity: An up-to-date overview of scRNA-seq data generation and analysis

por Carangelo, Giulia, Magi, Alberto, Semeraro, Roberto
Publicado 2022

Detection of Genomic Structural Variants from Next-Generation Sequencing Data

por Tattini, Lorenzo, D’Aurizio, Romina, Magi, Alberto
Publicado 2015

SLMSuite: a suite of algorithms for segmenting genomic profiles

por Orlandini, Valerio, Provenzano, Aldesia, Giglio, Sabrina, Magi, Alberto
Publicado 2017

Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm

por Magi, Alberto, Benelli, Matteo, Yoon, Seungtai, Roviello, Franco, Torricelli, Francesca
Publicado 2011

NanoR: A user-friendly R package to analyze and compare nanopore sequencing data

por Bolognini, Davide, Bartalucci, Niccolò, Mingrino, Alessandra, Vannucchi, Alessandro Maria, Magi, Alberto
Publicado 2019

TRiCoLOR: tandem repeat profiling using whole-genome long-read sequencing data

por Bolognini, Davide, Magi, Alberto, Benes, Vladimir, Korbel, Jan O, Rausch, Tobias
Publicado 2020

WNP: A Novel Algorithm for Gene Products Annotation from Weighted Functional Networks

por Magi, Alberto, Tattini, Lorenzo, Benelli, Matteo, Giusti, Betti, Abbate, Rosanna, Ruffo, Stefano
Publicado 2012

Bioinformatics for Next Generation Sequencing Data

por Magi, Alberto, Benelli, Matteo, Gozzini, Alessia, Girolami, Francesca, Torricelli, Francesca, Brandi, Maria Luisa
Publicado 2010

Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2

por D'Aurizio, Romina, Pippucci, Tommaso, Tattini, Lorenzo, Giusti, Betti, Pellegrini, Marco, Magi, Alberto
Publicado 2016

Genetic Bases of Bicuspid Aortic Valve: The Contribution of Traditional and High-Throughput Sequencing Approaches on Research and Diagnosis

por Giusti, Betti, Sticchi, Elena, De Cario, Rosina, Magi, Alberto, Nistri, Stefano, Pepe, Guglielmina
Publicado 2017

AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomics

por Magi, Alberto, Giangregorio, Tania, Semeraro, Roberto, Carangelo, Giulia, Palombo, Flavia, Romeo, Giovanni, Seri, Marco, Pippucci, Tommaso
Publicado 2020

Bicuspid Aortic Valve: Role of Multiple Gene Variants in Influencing the Clinical Phenotype

por Sticchi, Elena, De Cario, Rosina, Magi, Alberto, Giglio, Sabrina, Provenzano, Aldesia, Nistri, Stefano, Pepe, Guglielmina, Giusti, Betti
Publicado 2018

Charting differentially methylated regions in cancer with Rocker-meth

por Benelli, Matteo, Franceschini, Gian Marco, Magi, Alberto, Romagnoli, Dario, Biagioni, Chiara, Migliaccio, Ilenia, Malorni, Luca, Demichelis, Francesca
Publicado 2021

Rationale and pre-clinical evidences for the use of autologous cartilage micrografts in cartilage repair

por Viganò, Marco, Tessaro, Irene, Trovato, Letizia, Colombini, Alessandra, Scala, Marco, Magi, Alberto, Toto, Andrea, Peretti, Giuseppe, de Girolamo, Laura
Publicado 2018

Apolipoprotein(a) Kringle-IV Type 2 Copy Number Variation Is Associated with Venous Thromboembolism

por Sticchi, Elena, Magi, Alberto, Kamstrup, Pia R., Marcucci, Rossella, Prisco, Domenico, Martinelli, Ida, Mannucci, Pier Mannuccio, Abbate, Rosanna, Giusti, Betti
Publicado 2016