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Table 3 Mapping statistics for the NA12878 dataset (million reads)

From: Towards accurate detection and genotyping of expressed variants from whole transcriptome sequencing data

Run ID

Raw reads

Transcripts mapping

Genome mapping

Hard merge

Soft merge

SRR002052

12.6

2.9

4.3

4.5

4.7

SRR002054

12.9

3.9

5.7

5.9

6.2

SRR002060

25.7

4.4

6.7

7.0

7.3

SRR002055

11.4

3.7

5.5

5.6

5.9

SRR002063

23.0

3.5

5.6

5.8

6.0

SRR005091

13.9

3.3

4.9

5.0

5.2

SRR005096

14.4

0.6

1.0

1.1

1.1

Total

113.9

22.4

33.8

34.9

36.4