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Table 1 Summary of sequencing output and quality for each sample

From: Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients

Sample

Reads

Bases

Total

Mapped

On target

Mean depth

Aligned

ā‰„Q20

On target

Uniformitya

1

1,348,756

1,322,761

91.29Ā %

203.4

98.59Ā %

87.61Ā %

55.36Ā %

92.47Ā %

2

1,389,395

1,361,138

91.29Ā %

209.9

98.58Ā %

87.80Ā %

54.95Ā %

92.55Ā %

3

1,552,042

1,522,728

91.16Ā %

234.3

98.63Ā %

87.82Ā %

55.29Ā %

92.37Ā %

4

1,494,165

1,470,215

91.90Ā %

226.8

98.71Ā %

87.87Ā %

55.06Ā %

92.76Ā %

5

1,369,435

1,346,412

91.91Ā %

210.2

98.78Ā %

88.89Ā %

54.65Ā %

92.90Ā %

6

1,663,702

1,633,814

91.20Ā %

252.4

98.72Ā %

88.33Ā %

55.03Ā %

92.43Ā %

7

1,602,753

1,569,980

91.01Ā %

242.7

98.67Ā %

88.75Ā %

55.14Ā %

92.36Ā %

8

1,694,348

1,662,379

91.25Ā %

256.8

98.69Ā %

88.80Ā %

54.90Ā %

92.36Ā %

9

1,431,017

1,398,943

90.08Ā %

211.7

98.30Ā %

88.04Ā %

54.83Ā %

92.52Ā %

10

1,717,174

1,677,112

90.16Ā %

253.2

98.24Ā %

87.83Ā %

55.57Ā %

92.12Ā %

11

1,408,352

1,373,789

89.67Ā %

205.5

98.12Ā %

87.42Ā %

55.28Ā %

92.56Ā %

12

1,511,078

1,484,377

90.97Ā %

227.3

98.42Ā %

88.06Ā %

54.93Ā %

92.51Ā %

13

1,554,866

1,521,948

90.96Ā %

235.1

98.44Ā %

89.17Ā %

55.07Ā %

92.11Ā %

14

1,578,886

1,547,559

91.48Ā %

239.6

98.54Ā %

89.31Ā %

55.09Ā %

92.54Ā %

15

1,558,185

1,525,061

90.91Ā %

234.0

98.50Ā %

88.91Ā %

55.03Ā %

92.40Ā %

  1. aPercentage of target bases covered by at least 0.2Ɨ the average base read length