Benelli M - Search Results

1

A shifting level model algorithm that identifies aberrations in array-CGH data.

Magi A, Benelli M, Marseglia G, Nannetti G, Scordo MR, Torricelli F. Magi A, et al. Among authors: benelli m. Biostatistics. 2010 Apr;11(2):265-80. doi: 10.1093/biostatistics/kxp051. Epub 2009 Nov 30. Biostatistics. 2010. PMID: 19948744

2

A very fast and accurate method for calling aberrations in array-CGH data.

Benelli M, Marseglia G, Nannetti G, Paravidino R, Zara F, Bricarelli FD, Torricelli F, Magi A. Benelli M, et al. Biostatistics. 2010 Jul;11(3):515-8. doi: 10.1093/biostatistics/kxq008. Epub 2010 Mar 5. Biostatistics. 2010. PMID: 20207682

3

Discovering chimeric transcripts in paired-end RNA-seq data by using EricScript.

Benelli M, Pescucci C, Marseglia G, Severgnini M, Torricelli F, Magi A. Benelli M, et al. Bioinformatics. 2012 Dec 15;28(24):3232-9. doi: 10.1093/bioinformatics/bts617. Epub 2012 Oct 23. Bioinformatics. 2012. PMID: 23093608

4

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

Magi A, Benelli M, Yoon S, Roviello F, Torricelli F. Magi A, et al. Among authors: benelli m. Nucleic Acids Res. 2011 May;39(10):e65. doi: 10.1093/nar/gkr068. Epub 2011 Feb 14. Nucleic Acids Res. 2011. PMID: 21321017 Free PMC article.

5

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: benelli m. Bioinformatics. 2012 Feb 15;28(4):470-8. doi: 10.1093/bioinformatics/btr707. Epub 2011 Dec 23. Bioinformatics. 2012. PMID: 22199393

6

372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment.

Marseglia G, Scordo MR, Pescucci C, Nannetti G, Biagini E, Scandurra V, Gerundino F, Magi A, Benelli M, Torricelli F. Marseglia G, et al. Among authors: benelli m. Eur J Med Genet. 2012 Mar;55(3):216-21. doi: 10.1016/j.ejmg.2012.01.005. Epub 2012 Jan 25. Eur J Med Genet. 2012. PMID: 22333924

7

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: benelli m. Bioinformatics. 2014 Oct 15;30(20):2852-9. doi: 10.1093/bioinformatics/btu401. Epub 2014 Jun 24. Bioinformatics. 2014. PMID: 24966365

8

Bioinformatics for next generation sequencing data.

Magi A, Benelli M, Gozzini A, Girolami F, Torricelli F, Brandi ML. Magi A, et al. Among authors: benelli m. Genes (Basel). 2010 Sep 14;1(2):294-307. doi: 10.3390/genes1020294. Genes (Basel). 2010. PMID: 24710047 Free PMC article.

9

WNP: a novel algorithm for gene products annotation from weighted functional networks.

Magi A, Tattini L, Benelli M, Giusti B, Abbate R, Ruffo S. Magi A, et al. Among authors: benelli m. PLoS One. 2012;7(6):e38767. doi: 10.1371/journal.pone.0038767. Epub 2012 Jun 28. PLoS One. 2012. PMID: 22761703 Free PMC article.

10

Validation of a method for noninvasive prenatal testing for fetal aneuploidies risk and considerations for its introduction in the Public Health System.

Gerundino F, Giachini C, Contini E, Benelli M, Marseglia G, Giuliani C, Marin F, Nannetti G, Lisi E, Sbernini F, Periti E, Cordisco A, Colosi E, D'ambrosio V, Mazzi M, Rossi M, Staderini L, Minuti B, Pelo E, Cicatiello R, Maruotti GM, Sglavo G, Conti A, Frusconi S, Pescucci C, Torricelli F. Gerundino F, et al. Among authors: benelli m. J Matern Fetal Neonatal Med. 2017 Mar;30(6):710-716. doi: 10.1080/14767058.2016.1183633. Epub 2016 May 26. J Matern Fetal Neonatal Med. 2017. PMID: 27226231

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

100 results

Search Page