Identification and Characterization of Splicing Defects by Single-Molecule Real-Time Sequencing Technology (PacBio)
Author(s) -
Marco Savarese,
Talha Qureshi,
Annalaura Torella,
Pia Laine,
Teresa Giugliano,
Per Harald Jonson,
Mridul Johari,
Lars Paulín,
Giulio Piluso,
Petri Auvinen,
Vincenzo Nigro,
Bjarne Udd,
Peter Hackman
Publication year - 2020
Publication title -
journal of neuromuscular diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.366
H-Index - 23
eISSN - 2214-3602
pISSN - 2214-3599
DOI - 10.3233/jnd-200523
Subject(s) - rna splicing , computational biology , gene , genetics , dna sequencing , alternative splicing , biology , complementary dna , polymerase chain reaction , dna , rna , exon
Although DNA-sequencing is the most effective procedure to achieve a molecular diagnosis in genetic diseases, complementary RNA analyses are often required.Reverse-Transcription polymerase chain reaction (RT-PCR) is still a valuable option when the clinical phenotype and/or available DNA-test results address the diagnosis toward a gene of interest or when the splicing effect of a single variant needs to be assessed.We use Single-Molecule Real-Time sequencing to detect and characterize splicing defects and single nucleotide variants in well-known disease genes (DMD, NF1, TTN). After proper optimization, the procedure could be used in the diagnostic setting, simplifying the workflow of cDNA analysis.
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