Browse Dataset Files
Aligned reads from specific genomic locations derived from Illumina HiSeqX and HiSeq2000 whole genome sequence data
|EGAD00001003513||HiSeq X Ten,Illumina HiSeq 2000||3001|
This dataset includes bam files from 3,001 samples. These bam files include all read pairs where at least one of the reads aligns within 1kb of the C9orf72 repeat expansion. Additionally, these bam files also contain reads that are aligned to any of 29 pre-determined off target locations where the aligners are known to mis-align reads associated with this repeat expansion. These samples were sequenced using a combination of 2x100bp reads on an Illumina HiSeq2000 and 2x150bp reads on an Illumina HiSeqX sequencer and aligned using the Isaac aligner.