From: AluScan: a method for genome-wide scanning of sequence and structure variations in the human genome
 | Control | Glioma |
---|---|---|
Total initial reads (bp) | 896,661,780 | 1,065,234,324 |
Initial reads (bp) mapped to GRCh37.p2 | 836,745,196 | 983,798,813 |
Genomic regions mapped (bp) with coverage ≥ 1 | 58,876,070 | 64,297,421 |
Reads mapped (bp) with coverage ≥ 10 | 717,228,580 | 853,715,563 |
Genomic regions mapped with coverage ≥ 10: | ||
   Total regions (bp) | 10,638,683 | 11,846,868 |
   Average depth (x) | 67.4 | 72.1 |
   Inter-Alu sequences mapped (bp) | 10,149,445 | 11,275,690 |
   Genic sequences mapped (bp) | 5,644,023 | 6,274,433 |
   Genic sequences mapped as % of total mapped regions | 53.1% | 53.0% |
   Excess in genic sequencesa | 13.1% | 13.0% |
   Number of genes with mapped region | 8,502 | 9,205 |
   Number of cancer candidate genesb with mapped region | 2,921 | 3,096 |
Cancer candidate genesb with mapped region as % of genes with mapped region | 34.4% | 33.6% |
   Excess in cancer candidate genesc | 8.4% | 7.6% |