IT202200006119A1 - Method for implementing the design of synthetic nucleic acid molecules for gene therapies in rare diseases. - Google Patents

Method for implementing the design of synthetic nucleic acid molecules for gene therapies in rare diseases. Download PDF

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Publication number
IT202200006119A1
IT202200006119A1 IT102022000006119A IT202200006119A IT202200006119A1 IT 202200006119 A1 IT202200006119 A1 IT 202200006119A1 IT 102022000006119 A IT102022000006119 A IT 102022000006119A IT 202200006119 A IT202200006119 A IT 202200006119A IT 202200006119 A1 IT202200006119 A1 IT 202200006119A1
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IT
Italy
Prior art keywords
implementing
design
nucleic acid
acid molecules
synthetic nucleic
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IT102022000006119A
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English (en)
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Alessandra Ferlini
Rachele Rossi
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Univ Degli Studi Di Ferrara
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Priority to IT102022000006119A priority Critical patent/IT202200006119A1/it
Publication of IT202200006119A1 publication Critical patent/IT202200006119A1/it

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    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B30/00ICT specially adapted for sequence analysis involving nucleotides or amino acids
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B20/00ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
    • G16B20/20Allele or variant detection, e.g. single nucleotide polymorphism [SNP] detection
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B40/00ICT specially adapted for biostatistics; ICT specially adapted for bioinformatics-related machine learning or data mining, e.g. knowledge discovery or pattern finding
    • G16B40/30Unsupervised data analysis

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  • Life Sciences & Earth Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Medical Informatics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Biophysics (AREA)
  • Bioinformatics & Computational Biology (AREA)
  • Biotechnology (AREA)
  • Evolutionary Biology (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Theoretical Computer Science (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Analytical Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Data Mining & Analysis (AREA)
  • Artificial Intelligence (AREA)
  • Bioethics (AREA)
  • Computer Vision & Pattern Recognition (AREA)
  • Databases & Information Systems (AREA)
  • Epidemiology (AREA)
  • Evolutionary Computation (AREA)
  • Public Health (AREA)
  • Software Systems (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
IT102022000006119A 2022-03-29 2022-03-29 Method for implementing the design of synthetic nucleic acid molecules for gene therapies in rare diseases. IT202200006119A1 (it)

Priority Applications (1)

Application Number Priority Date Filing Date Title
IT102022000006119A IT202200006119A1 (it) 2022-03-29 2022-03-29 Method for implementing the design of synthetic nucleic acid molecules for gene therapies in rare diseases.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT102022000006119A IT202200006119A1 (it) 2022-03-29 2022-03-29 Method for implementing the design of synthetic nucleic acid molecules for gene therapies in rare diseases.

Publications (1)

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IT202200006119A1 true IT202200006119A1 (it) 2023-09-29

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Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20170368198A1 (en) * 2016-06-21 2017-12-28 The University Of North Carolina At Chapel Hill Optimized mini-dystrophin genes and expression cassettes and their use
WO2021226461A1 (en) * 2020-05-07 2021-11-11 Translate Bio, Inc. Generation of optimized nucleotide sequences

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20170368198A1 (en) * 2016-06-21 2017-12-28 The University Of North Carolina At Chapel Hill Optimized mini-dystrophin genes and expression cassettes and their use
WO2021226461A1 (en) * 2020-05-07 2021-11-11 Translate Bio, Inc. Generation of optimized nucleotide sequences

Non-Patent Citations (7)

* Cited by examiner, † Cited by third party
Title
BIRKHOLTZ ET AL., MALARIA J, vol. 7, 2008, pages 197 - 217
FANG M ET AL: "O.11Dystrophin gene codon usage lacks extreme codon bias and shows non-random codon distribution of disease-causing mutations", NEUROMUSCULAR DISORDERS, ELSEVIER LTD, GB, vol. 29, 29 September 2019 (2019-09-29), XP085844575, ISSN: 0960-8966, [retrieved on 20190929], DOI: 10.1016/J.NMD.2019.06.029 *
GOULD N ET AL: "Computational tools and algorithms for designing customized synthetic genes", FRONTIERS IN BIOENGINEERING AND BIOTECHNOLOGY, FRONTIERS RESEARCH FOUNDATION, CH, vol. 2, 6 October 2014 (2014-10-06), pages 41 - 1, XP002755946, ISSN: 2296-4185, [retrieved on 20140101], DOI: 10.3389/FBIOE.2014.00041 *
NAKAMURA ET AL., NUCLEIC ACIDS RES., vol. 28, 2000, pages 292
ROSSI RACHELE ET AL: "Calculating and comparing codon usage values in rare disease genes highlights codon clustering with disease-and tissue- specific hierarchy", PLOS ONE, vol. 17, no. 3, 31 March 2022 (2022-03-31), pages e0265469, XP055982992, DOI: 10.1371/journal.pone.0265469 *
SHARPLI, NUCLEIC ACIDS RES., vol. 15, 1987, pages 1281 - 95
WEISSBACH H: "Years of Molecular Biology", vol. 736, 2012, ELSEVIER, article "Syntax of referencing in Molecular Mechanisms of Protein Biosynthesis", pages: 3 - 5

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IT202200006119A1 (it) Method for implementing the design of synthetic nucleic acid molecules for gene therapies in rare diseases.