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Genome-wide copy number analysis in pediatric glioblastoma multiforme.
Giunti L, Pantaleo M, Sardi I, Provenzano A, Magi A, Cardellicchio S, Castiglione F, Tattini L, Novara F, Buccoliero AM, de Martino M, Genitori L, Zuffardi O, Giglio S. Giunti L, et al. Among authors: tattini l. Am J Cancer Res. 2014 May 26;4(3):293-303. eCollection 2014. Am J Cancer Res. 2014. PMID: 24959384 Free PMC article.
Read count approach for DNA copy number variants detection.
Magi A, Tattini L, Pippucci T, Torricelli F, Benelli M. Magi A, et al. Among authors: tattini l. Bioinformatics. 2012 Feb 15;28(4):470-8. doi: 10.1093/bioinformatics/btr707. Epub 2011 Dec 23. Bioinformatics. 2012. PMID: 22199393
H3M2: detection of runs of homozygosity from whole-exome sequencing data.
Magi A, Tattini L, Palombo F, Benelli M, Gialluisi A, Giusti B, Abbate R, Seri M, Gensini GF, Romeo G, Pippucci T. Magi A, et al. Among authors: tattini l. Bioinformatics. 2014 Oct 15;30(20):2852-9. doi: 10.1093/bioinformatics/btu401. Epub 2014 Jun 24. Bioinformatics. 2014. PMID: 24966365
EXCAVATOR: detecting copy number variants from whole-exome sequencing data.
Magi A, Tattini L, Cifola I, D'Aurizio R, Benelli M, Mangano E, Battaglia C, Bonora E, Kurg A, Seri M, Magini P, Giusti B, Romeo G, Pippucci T, De Bellis G, Abbate R, Gensini GF. Magi A, et al. Among authors: tattini l. Genome Biol. 2013;14(10):R120. doi: 10.1186/gb-2013-14-10-r120. Genome Biol. 2013. PMID: 24172663 Free PMC article.
22 results