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Table 1 Mapping statistics

From: Influence of RNA extraction methods and library selection schemes on RNA-seq data

Group

Sample

All reads

Mapped reads

Pairs

Mapped, MAPQ > 1

Mapped on exons (%)

Mapped on introns (%)

Mapped on introns (%) mapped to non annotated regions (%)

Mapped on rRNA (%)

Mapped on mitochondrial DNA (%)

Unique starting position (%)

PolyA Trizol

Tot_RNA1

101028616

93699257

78996022

83038355

86,7

10,7

2,6

0,31

4,80

32,4

Tot_RNA2

103480788

96072826

81214720

84983881

PolyA Qiagen

Tot_RNA3

100766522

100766522

76780490

82231228

91,3

6,6

2,1

0,30

4,58

28,5

Tot_RNA4

109645220

109645220

83720316

89300384

RiboZ Trizol

Tot_RNA1

109221096

103587793

92825224

85242138

60,6

35,1

4,3

0,04

0,39

51,5

Tot_RNA2

113936740

107997806

96763362

90980604

RiboZ Qiagen

Tot_RNA3

118950948

118950948

110394536

91193892

81,6

15,6

2,8

0,02

0,28

35,1

Tot_RNA4

112056778

112056778

88450950

86755352

RiboZ cytoplasmic

Cyt_RNA5

111517838

102989353

86770814

87248867

87,1

10,3

2,6

0,03

0,56

31,3

Cyt_RNA6

102998772

94630661

79109400

87248867

RiboZ nuclear

Nuc_RNA7

126297526

122854406

116663678

115579529

31,1

60,8

8,2

0,01

0,05

65,2

Nuc_RNA8

127905406

124011269

117109650

116428981

  1. The numbers of mapped sequence reads are given as absolute numbers. Percentages are calculated according to the total number of reliable reads (MAPQ > 1). The number of unique starting positions is a measure of the library complexity.