Martin Wendlandt

Transcript capture and ultradeep long-read RNA sequencing (CAPLRseq) to diagnose HNPCC/Lynch syndrome

A. Laner, M. Morak, Verena Steinke-Lange, 2023, Journal of Medical Genetics.

Parallel in-depth analysis of repeat expansions in ataxia patients by long-read sequencing.

W. Heide, T. Neuhann, B. Schoser, 2022, Brain : a journal of neurology.