Fig. 6
From: Interrogating the “unsequenceable” genomic trinucleotide repeat disorders by long-read sequencing
The analysis of ATXN3 in HX1 using three different sequencing techniques. a Whole-genome long-read sequencing with ~100X coverage. b PCR-based long-read sequencing with three randomly down-sampled datasets, each with ~100X coverage. c Sanger sequencing. All methods concordantly predicted that there were 14 CAG repeats in ATXN3