SRX2029848 small RNA-seq of Panax notoginseng root sample r2 SRP082250 PRJNA339204 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624153 SAMN05582977 small RNA-seq of Panax notoginseng root sample r2 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030588 small RNA-seq of Panax notoginseng root sample r4 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624756 SAMN05582980 small RNA-seq of Panax notoginseng root sample r2 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030589 small RNA-seq of Panax notoginseng root sample r7 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624757 SAMN05582981 small RNA-seq of Panax notoginseng root sample r7 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030590 small RNA-seq of Panax notoginseng root sample r8 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624758 SAMN05582982 small RNA-seq of Panax notoginseng root sample r8 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030591 small RNA-seq of Panax notoginseng root sample r9 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624759 SAMN05582983 small RNA-seq of Panax notoginseng root sample r9 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030592 small RNA-seq of Panax notoginseng root sample r16 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624760 SAMN05582984 small RNA-seq of Panax notoginseng root sample r16 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030593 small RNA-seq of Panax notoginseng root sample r21 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624761 SAMN05582985 small RNA-seq of Panax notoginseng root sample r21 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030595 small RNA-seq of Panax notoginseng root sample r25 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624763 SAMN05582986 small RNA-seq of Panax notoginseng root sample r25 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030596 small RNA-seq of Panax notoginseng root sample r28 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624764 SAMN05582987 small RNA-seq of Panax notoginseng root sample r28 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030608 small RNA-seq of Panax notoginseng root sample r32 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624776 SAMN05582988 small RNA-seq of Panax notoginseng root sample r32 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030610 small RNA-seq of Panax notoginseng root sample r43 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624778 SAMN05582989 small RNA-seq of Panax notoginseng root sample r43 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030611 small RNA-seq of Panax notoginseng root sample r44 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624779 SAMN05582990 small RNA-seq of Panax notoginseng root sample r44 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030612 small RNA-seq of Panax notoginseng root sample r46 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624780 SAMN05582991 small RNA-seq of Panax notoginseng root sample r46 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030613 small RNA-seq of Panax notoginseng root sample r47 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624781 SAMN05582992 small RNA-seq of Panax notoginseng root sample r47 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030614 small RNA-seq of Panax notoginseng root sample r48 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624782 SAMN05582993 small RNA-seq of Panax notoginseng root sample r48 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030615 small RNA-seq of Panax notoginseng root sample r53 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624783 SAMN05582994 small RNA-seq of Panax notoginseng root sample r53 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000 SRX2030616 small RNA-seq of Panax notoginseng root sample r54 SRP082250 The roots of the collected P. notoginseng were frozen in liquid nitrogen immediately. The samples were stored at -80 degrees Celsius until RNA extraction. Total RNAs were extracted from each tissue using the Trizol reagent according to the manufacturer's protocol. The integrity of the RNAs were checked with an ultraviolet spectrophotometry and 2100 BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The small RNAs of the root samples were isolated from total RNAs and were sequenced using Illumina HiSeq 2000 equipment. The small RNAs of Panax notoginseng (Burk.) F.H. Chen roots were sequenced to get the abundance of small regulatory RNAs, such as miRNAs and tasiRNAs. SRS1624784 SAMN05582995 small RNA-seq of Panax notoginseng root sample r54 miRNA-Seq TRANSCRIPTOMIC size fractionation 50 0 Application Read Forward 1 Illumina HiSeq 2000