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Table 1 Control and glioma sequence outputs from AluScan

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%

  1. aExcess in % genic sequences with mapped region relative to the 40% genic sequences in the reference human genome.
  2. bCancer candidate genes refer to genes listed in Gene Ranker: TCGA GBM 6000.
  3. cExcess in % cancer candidate genes with mapped region relative to the 26% of total human genes included in Gene Ranker: TCGA GBM 6000.