Read count approach for DNA copy number variants detection. - Alberto Magi; Lorenzo Tattini; Tommaso Pippucci; Francesca Torricelli; Matteo Benelli (Bioinform., 2012)

H3M2: detection of runs of homozygosity from whole-exome sequencing data. - Alberto Magi; Lorenzo Tattini; Flavia Palombo; Matteo Benelli; Alessandro Gialluisi; Betti Giusti; Rosanna Abbate; Marco Seri; Gian Franco Gensini; Giovanni Romeo; Tommaso Pippucci (Bioinform., 2014)

The Source of the Data Flood: Sequencing Technologies. - Alberto Magi; Nadia Pisanti; Lorenzo Tattini (ERCIM News, 2016)

A Fast Algorithm for Large Common Connected Induced Subgraphs. - Alessio Conte; Roberto Grossi; Andrea Marino 001; Lorenzo Tattini; Luca Versari (AlCoB, 2017)

Characterization of MinION nanopore data for resequencing analyses. - Alberto Magi; Betti Giusti; Lorenzo Tattini (Briefings Bioinform., 2017)

A fast discovery algorithm for large common connected induced subgraphs. - Alessio Conte; Roberto Grossi; Andrea Marino 001; Lorenzo Tattini; Luca Versari (Discret. Appl. Math., 2019)

phyBWT: Alignment-Free Phylogeny via eBWT Positional Clustering. - Veronica Guerrini; Alessio Conte; Roberto Grossi; Gianni Liti; Giovanna Rosone; Lorenzo Tattini (WABI, 2022)

phyBWT2: phylogeny reconstruction via eBWT positional clustering. - Veronica Guerrini; Alessio Conte; Roberto Grossi; Gianni Liti; Giovanna Rosone; Lorenzo Tattini (Algorithms Mol. Biol., 2023)

Subsequence-Based Indices for Genome Sequence Analysis. - Giovanni Buzzega; Alessio Conte; Veronica Guerrini; Giulia Punzi; Giovanna Rosone; Lorenzo Tattini (From Strings to Graphs, and Back Again, 2025)