Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing.

Pål Marius BjørnstadRagnhild AaløkkenJune ÅsheimArvind Y M SundaramCaroline N FeldeG Henriette ØstbyMarianne DallandWenche SjursenChristian CarrizosaMagnus D VigelandHanne S SorteYing ShengSarah L AriansenEli Marie GrindedalGregor D Gilfillan

Published in: European journal of human genetics : EJHG (2024)

Keyphrases

high resolution
single molecule
single cell
case report
high speed
genome wide
high density
solid state
high throughput sequencing