Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Loredana M. Genovese"'
Autor:
Loredana M. Genovese, Filippo Geraci, Lucia Corrado, Eleonora Mangano, Romina D'Aurizio, Roberta Bordoni, Marco Severgnini, Giovanni Manzini, Gianluca De Bellis, Sandra D'Alfonso, Marco Pellegrini
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
Polymorphic Tandem Repeat (PTR) is a common form of polymorphism in the human genome. A PTR consists in a variation found in an individual (or in a population) of the number of repeating units of a Tandem Repeat (TR) locus of the genome with respect
Externí odkaz:
https://doaj.org/article/92c24b9e36fc4c92bb40664c827e91b9
Publikováno v:
Bioinformatics (Oxf., Print) 35 (2018): 914–922. doi:10.1093/bioinformatics/bty747
info:cnr-pdr/source/autori:L. M. Genovese(1); M. M. Mosca (2); M. Pellegrini; F. Geraci (1)/titolo:Dot2dot: accurate whole-genome tandem repeats discovery/doi:10.1093%2Fbioinformatics%2Fbty747/rivista:Bioinformatics (Oxf., Print)/anno:2018/pagina_da:914/pagina_a:922/intervallo_pagine:914–922/volume:35
Bioinformatics
info:cnr-pdr/source/autori:L. M. Genovese(1); M. M. Mosca (2); M. Pellegrini; F. Geraci (1)/titolo:Dot2dot: accurate whole-genome tandem repeats discovery/doi:10.1093%2Fbioinformatics%2Fbty747/rivista:Bioinformatics (Oxf., Print)/anno:2018/pagina_da:914/pagina_a:922/intervallo_pagine:914–922/volume:35
Bioinformatics
Motivation Large-scale sequencing projects have confirmed the hypothesis that eukaryotic DNA is rich in repetitions whose functional role needs to be elucidated. In particular, tandem repeats (TRs) (i.e. short, almost identical sequences that lie adj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da73fb98db87978770981437b3f80f37
https://doi.org/10.1093/bioinformatics/bty747
https://doi.org/10.1093/bioinformatics/bty747
Autor:
Filippo Geraci, Loredana M. Genovese
Publikováno v:
Journal of Software. 13:300-316
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::610f6bb0852602a9987021eb8ff88acb
https://doi.org/10.17706/jsw.13.5.300-316
https://doi.org/10.17706/jsw.13.5.300-316
Publikováno v:
Bioinformatics Italian Society (BITS) Annual Meeting 2014, Roma, 2014
info:cnr-pdr/source/autori:Loredana M. Genovese, Filippo Geraci, Marco Pellegrini/congresso_nome:Bioinformatics Italian Society (BITS) Annual Meeting 2014/congresso_luogo:Roma/congresso_data:2014/anno:2014/pagina_da:/pagina_a:/intervallo_pagine
info:cnr-pdr/source/autori:Loredana M. Genovese, Filippo Geraci, Marco Pellegrini/congresso_nome:Bioinformatics Italian Society (BITS) Annual Meeting 2014/congresso_luogo:Roma/congresso_data:2014/anno:2014/pagina_da:/pagina_a:/intervallo_pagine
Motivation: Protein architectures form a complex multilayered hierarchy.The primary linear sequence of amino acids residues arranges itself in 3-dimensional space so to form localstructures (secondary and super-secondary structures, and extends up to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::a2fed61c829b5eb0b9439d5ee203b3ac
http://www.cnr.it/prodotto/i/295161
http://www.cnr.it/prodotto/i/295161
Publikováno v:
IEEE/ACM transactions on computational biology and bioinformatics
4 (2008): 492–502. doi:10.1109/TCBB.2008.67
info:cnr-pdr/source/autori:[1] Genovese L. M., [1] Geraci F., [1] Pellegrini M./titolo:SpeedHap: An Accurate Heuristic for the Single Individual SNP Haplotyping Problem with Many Gaps, High Reading Error Rate and Low Coverage/doi:10.1109%2FTCBB.2008.67/rivista:IEEE%2FACM transactions on computational biology and bioinformatics (Print)/anno:2008/pagina_da:492/pagina_a:502/intervallo_pagine:492–502/volume:4
4 (2008): 492–502. doi:10.1109/TCBB.2008.67
info:cnr-pdr/source/autori:[1] Genovese L. M., [1] Geraci F., [1] Pellegrini M./titolo:SpeedHap: An Accurate Heuristic for the Single Individual SNP Haplotyping Problem with Many Gaps, High Reading Error Rate and Low Coverage/doi:10.1109%2FTCBB.2008.67/rivista:IEEE%2FACM transactions on computational biology and bioinformatics (Print)/anno:2008/pagina_da:492/pagina_a:502/intervallo_pagine:492–502/volume:4
Single nucleotide polymorphism (SNP) is the most frequent form of DNA variation. The set of SNP's present in a chromosome (called the em haplotype) is of interest in a wide area of applications in molecular biology and biomedicine, including diagnost
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3a9422c621eeecb6a60fc7ab58f618f
https://pubmed.ncbi.nlm.nih.gov/18989037
https://pubmed.ncbi.nlm.nih.gov/18989037
Autor:
Shib Sankar Bhowmick, Indrajit Saha, Debotosh Bhattacharjee, Loredana M Genovese, Filippo Geraci
Publikováno v:
PLoS ONE, Vol 13, Iss 7, p e0200353 (2018)
MicroRNAs are small non-coding RNAs that influence gene expression by binding to the 3' UTR of target mRNAs in order to repress protein synthesis. Soon after discovery, microRNA dysregulation has been associated to several pathologies. In particular,
Externí odkaz:
https://doaj.org/article/b003ef4674044eb69d8213df636851a9