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. 2020 Dec 9;21:879. doi: 10.1186/s12864-020-07275-6

Table 1.

Genomic categories that are mapped by sRNA reads by size-fractionated total RNA libraries (TAP cloning method)

Size-fractionated total RNA libraries, 5′ P-independent cloning, WT
Categories 15-30nt (27nt sRNAs) 30-45nt # (27nt and 31nt sRNAs) 3'-end trimmed * (31nt sRNAs trimmed off oligo-As)
Total reads 624,954 411,419
Unique (unique/total reads) 242,277 (38.8%) 171,309 (41.6%) 86,031
tRNAa,S 2,343 (1.0%) 2,848 (1.7%) 1,035 (1.2%)
rRNAa,S 12,957 (5.3%) 18,235 (10.6%) 450 (0.5%)
LINEsa,AS 16,424 (6.8%) 8,492 (5.0%) 23,999 (27.9%)
Map to rest of genomea 172,261 (71.1%) 55,703 (32.5%) 36,651 (42.6%)
Map to predicted ORFsa,AS 124,770 (51.5%) 37,145 (21.7%) 27,508 (32%)
Not mapped to genome (%) 38,292 (15.8%) 86,031 (50.2%) 23,896 (27.8%)

a Number of unique reads divided by total unique reads

S Most reads are in sense orientation

AS Most reads are in antisense orientation

# Only 27nt sRNAs can be mapped to the genome, not 31nt sRNAs

* The 31nt sRNAs (non-mapped reads in 30-45nt library) were trimmed from 3' end into 27nt size, then they can be mapped to the genome.