Table 1 Statistical tables of mapped reads of paired-end.

From: Transcriptome profiling of cells exposed to particular and intense electromagnetic radiation emitted by the "SG-III" prototype laser facility

Sample_ID

total_reads

total_map

unique_map

multi_map

read1_map

read2_map

positive_map

negative_map

Control

45,139,792

42,281,404

(93.67%)

41,312,692

(91.52%)

968,712

(2.15%)

20,714,062

(45.89%)

20,598,630

(45.63%)

20,648,794

(45.74%)

20,663,898

(45.78%)

Low

45,879,270

42,769,425

(93.22%)

41,704,658

(90.9%)

1,064,767

(2.32%)

20,905,769

(45.57%)

20,798,889

(45.33%)

20,843,571

(45.43%)

20,861,087

(45.47%)

High

45,898,106

42,915,108 (93.5%)

41,790,531 (91.05%)

1,124,577 (2.45%)

20,935,227 (45.61%)

20,855,304 (45.44%)

20,887,532 (45.51%)

20,902,999 (45.54%)

  1. total_reads: The number of clean reads sequencing data after quality control.
  2. total_map: The number and percentage of clean reads compared to the reference genome unique_map: The number and percentage of reads at unique locations compared to the reference genome.
  3. multi_map: The number and percentage of reads at multiple locations compared to the reference genome.
  4. read1_map: The number and percentage of read1 compared to the reference genome.
  5. read2_map: The number and percentage of read1 compared to the reference genome.
  6. positive_map: The number and percentage of reads on the positive chain compared to the reference genome.
  7. negative_map: The number and percentage of reads on the negative chain compared to the reference genome.
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