This dataset includes bam files from 58 samples. These bam files include all read pairs where at least one of the reads aligns within 1kb of the HTT repeat expansion. These samples were sequenced usin
We have developed a technique based on selective restriction digestion and size fractionation to enrich for centromeric DNA from human cells. Combining enzymes capable of cutting at high frequency thr
Background: 22q11.2 deletion syndrome (22q11.2DS) is a disorder caused when a small part of chromosome 22 is missing. Diagnosis is currently established by the identification of a heterozygous deletio
Summary of targeted sequencing data in multiple replicates for dCATCH-Seq and CATCH-Seq. Table S2. Comparison of Indel calls between dCATCH-Seq and CATCH-Seq. Table S3. HLA gene typing for dCATCH-Seq.