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Author Correction: High-resolution Nanopore methylome-maps reveal random hyper-methylation at CpG-poor regions as driver of chemoresistance in leukemias.
Magi A, Mattei G, Mingrino A, Caprioli C, Ronchini C, Frigè G, Semeraro R, Bolognini D, Rambaldi A, Candoni A, Colombo E, Mazzarella L, Pelicci PG. Magi A, et al. Commun Biol. 2023 Apr 25;6(1):455. doi: 10.1038/s42003-023-04842-x. Commun Biol. 2023. PMID: 37185600 Free PMC article. No abstract available.
Read count approach for DNA copy number variants detection.
Magi A, Tattini L, Pippucci T, Torricelli F, Benelli M. Magi A, et al. Bioinformatics. 2012 Feb 15;28(4):470-8. doi: 10.1093/bioinformatics/btr707. Epub 2011 Dec 23. Bioinformatics. 2012. PMID: 22199393
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. Genome Biol. 2013;14(10):R120. doi: 10.1186/gb-2013-14-10-r120. Genome Biol. 2013. PMID: 24172663 Free PMC article.
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: magi a. Am J Cancer Res. 2014 May 26;4(3):293-303. eCollection 2014. Am J Cancer Res. 2014. PMID: 24959384 Free PMC article.
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. Bioinformatics. 2014 Oct 15;30(20):2852-9. doi: 10.1093/bioinformatics/btu401. Epub 2014 Jun 24. Bioinformatics. 2014. PMID: 24966365
Epilepsy with auditory features: A heterogeneous clinico-molecular disease.
Pippucci T, Licchetta L, Baldassari S, Palombo F, Menghi V, D'Aurizio R, Leta C, Stipa C, Boero G, d'Orsi G, Magi A, Scheffer I, Seri M, Tinuper P, Bisulli F. Pippucci T, et al. Among authors: magi a. Neurol Genet. 2015 May 14;1(1):e5. doi: 10.1212/NXG.0000000000000005. eCollection 2015 Jun. Neurol Genet. 2015. PMID: 27066544 Free PMC article.
131 results