Input files of two tumor samples from a brain tumor patient. For each sample, there are two bed files for the highly amplified genomic regions: CNA_region_raw_*.bed and CNA_region_refined_*.bed.
CNA_region_raw_D.bed
: the highly amplified segments extracted from CONSERTING somatic copy number alteration (SCNA) output of the diagnosis sample.CNA_region_raw_R.bed
: the highly amplified segments extracted from CONSERTING somatic copy number alteration (SCNA) output of the relapse sample.CNA_region_refined_D.bed
: refined segment boundaries based on manual inspection of each segment’s coverage on IGV and the Blat output of the diagnosis sample.CNA_region_refined_R.bed
: refined segment boundaries based on manual inspection of each segment’s coverage on IGV and the Blat output of the relapse sample.mini_SJHGG019_E.bam
: mini bam for the diagnosis sample.mini_SJHGG019_E.bam.bai
: index file for the mini bam of the diagnosis sample.mini_SJHGG019_S.bam
: mini bam for the relapse sample.mini_SJHGG019_S.bam.bai
: index file for the mini bam of the relapse sample.