Table 2.

The data for the sequencing reads that mapped to the reference genome.

Mapping statistics	C1	C2	C3	M1	M2	M3
Total reads	25,927,296 (100%)	21,924,166 (100%)	20,808,688 (100%)	20,280,672 (100%)	24,686,554 (100%)	26,115,966 (100%)
Total mapped	22,227,826 (85.73%)	18,834,354 (85.91%)	17,754,405 (85.32%)	17,355,918 (85.58%)	20,950,545 (84.87%)	22,561,967 (86.39%)
Multiple mapped	1,194,742 (4.61%)	1,158,291 (5.28%)	787,789 (3.79%)	803,162 (3.96%)	798,262 (3.23%)	887,175 (3.4%)
Uniquely mapped	21,033,084 (81.12%)	17,676,063 (80.62%)	16,966,616 (81.54%)	16,552,756 (81.62%)	20,152,283 (81.63%)	21,674,792 (82.99%)
Reads mapped to “+”	10,510,392 (40.54%)	8,824,248 (40.25%)	8,466,976 (40.69%)	8,262,795 (40.74%)	10,073,579 (40.81%)	10,830,805 (41.47%)
Reads mapped to “−”	10,522,692 (40.59%)	8,851,815 (40.37%)	8,499,640 (40.85%)	8,289,961 (40.88%)	10,078,704 (40.83%)	10,843,987 (41.52%)
Nonsplice reads	11,296,626 (43.57%)	10,018,343 (45.7%)	10,020,095 (48.15%)	9,453,740 (46.61%)	11,610,290 (47.03%)	12,553,211 (48.07%)
Splice reads	9,736,458 (37.55%)	7,657,720 (34.93%)	6,946,521 (33.38%)	7,099,016 (35%)	8,541,993 (34.6%)	9,121,581 (34.93%)

C1, C2, and C3: control group; M1, M2, and M3: moxibustion group. “+” refers to the sense strand, and “−” refers to the antisense strand.