For example, the intronic repeat in NOP56, which causes spinocerebellar ataxia 36, had an average of 20× coverage, depending on the capture kit; repeats in UTRs, such as JPH3, DMPK, NOTCH2NLC and PPP2R2B (which cause Huntington disease-like 2, myotonic dystrophy type 1, neuronal intranuclear inclusion disease and spinocerebellar ataxia 12), were also captured and their genotypes predicted (Figure 5, Supplementary Table S2). The gene discussed is JPH3; the disease is neuronal intranuclear inclusion disease.