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
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
MHC_I_BRD2_alignments.zip - alignments of all potentially functional MHC-I exon2, exon 3 and BRD2 allelesTAP_alignments.zip - alignments of coding sequences extracted from reference sequences of TAP1
Input data and bash scripts to create coordinates of segments on reference sequences. Usage:1. decompres and untar .gz files2. run get_ind_cov.sh - produces coverage files for each species2. run se
