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Targeted nanopore sequencing enables complete characterisation of structural deletions initially identified using exon-based short-read sequencing strategies.

Benjamin McClintonLaura A CrinnionMartin McKibbinRajarshi MukherjeeJames A PoulterClaire E L SmithManir AliChristopher Mark WatsonChris F InglehearnCarmel Toomes
Published in: Molecular genetics & genomic medicine (2023)
In this study, a quick, accurate and cost - effective method is described to characterise deletions identified from exome, and similar data, using nanopore sequencing.
Keyphrases
  • single molecule
  • single cell
  • electronic health record
  • high resolution
  • solid state
  • copy number
  • dna methylation
  • mass spectrometry