SRX3644444 FLOR1 SRP132090 PRJNA431782 Leaf or flower samples, were grounded to fine powder. According to the manufacturers protocols, total RNAs were isolated using the Trizol reagent followed by treatment with RNase-free DNase I. The quality of RNAs was checked using Agilent 2100 Bioanalyzer. RNA-Seq libraries were prepared and sequenced on the HiSeq 2000 system, following the manufacturer s instructions. SRS2909244 SAMN08405648 FLOR1 RNA-Seq TRANSCRIPTOMIC RANDOM Illumina HiSeq 2000 SRX3644445 LF3 SRP132090 PRJNA431782 Leaf or flower samples, were grounded to fine powder. According to the manufacturers protocols, total RNAs were isolated using the Trizol reagent followed by treatment with RNase-free DNase I. The quality of RNAs was checked using Agilent 2100 Bioanalyzer. RNA-Seq libraries were prepared and sequenced on the HiSeq 2000 system, following the manufacturer s instructions. SRS2909243 SAMN08405647 LF3 RNA-Seq TRANSCRIPTOMIC RANDOM Illumina HiSeq 2000 SRX3644446 LF2 SRP132090 PRJNA431782 Leaf or flower samples, were grounded to fine powder. According to the manufacturers protocols, total RNAs were isolated using the Trizol reagent followed by treatment with RNase-free DNase I. The quality of RNAs was checked using Agilent 2100 Bioanalyzer. RNA-Seq libraries were prepared and sequenced on the HiSeq 2000 system, following the manufacturer s instructions. SRS2909243 SAMN08405647 LF2 RNA-Seq TRANSCRIPTOMIC RANDOM Illumina HiSeq 2000 SRX3644447 LF1 SRP132090 PRJNA431782 Leaf or flower samples, were grounded to fine powder. According to the manufacturers protocols, total RNAs were isolated using the Trizol reagent followed by treatment with RNase-free DNase I. The quality of RNAs was checked using Agilent 2100 Bioanalyzer. RNA-Seq libraries were prepared and sequenced on the HiSeq 2000 system, following the manufacturer s instructions. SRS2909243 SAMN08405647 LF1 RNA-Seq TRANSCRIPTOMIC RANDOM Illumina HiSeq 2000 SRX3644448 FLOR5 SRP132090 PRJNA431782 Leaf or flower samples, were grounded to fine powder. According to the manufacturers protocols, total RNAs were isolated using the Trizol reagent followed by treatment with RNase-free DNase I. The quality of RNAs was checked using Agilent 2100 Bioanalyzer. RNA-Seq libraries were prepared and sequenced on the HiSeq 2000 system, following the manufacturer s instructions. SRS2909244 SAMN08405648 FLOR5 RNA-Seq TRANSCRIPTOMIC RANDOM Illumina HiSeq 2000 SRX3644449 FLOR4 SRP132090 PRJNA431782 Leaf or flower samples, were grounded to fine powder. According to the manufacturers protocols, total RNAs were isolated using the Trizol reagent followed by treatment with RNase-free DNase I. The quality of RNAs was checked using Agilent 2100 Bioanalyzer. RNA-Seq libraries were prepared and sequenced on the HiSeq 2000 system, following the manufacturer s instructions. SRS2909244 SAMN08405648 FLOR4 RNA-Seq TRANSCRIPTOMIC RANDOM Illumina HiSeq 2000 SRX3644450 FLOR3 SRP132090 PRJNA431782 Leaf or flower samples, were grounded to fine powder. According to the manufacturers protocols, total RNAs were isolated using the Trizol reagent followed by treatment with RNase-free DNase I. The quality of RNAs was checked using Agilent 2100 Bioanalyzer. RNA-Seq libraries were prepared and sequenced on the HiSeq 2000 system, following the manufacturer s instructions. SRS2909244 SAMN08405648 FLOR3 RNA-Seq TRANSCRIPTOMIC RANDOM Illumina HiSeq 2000 SRX3644451 FLOR2 SRP132090 PRJNA431782 Leaf or flower samples, were grounded to fine powder. According to the manufacturers protocols, total RNAs were isolated using the Trizol reagent followed by treatment with RNase-free DNase I. The quality of RNAs was checked using Agilent 2100 Bioanalyzer. RNA-Seq libraries were prepared and sequenced on the HiSeq 2000 system, following the manufacturer s instructions. SRS2909244 SAMN08405648 FLOR2 RNA-Seq TRANSCRIPTOMIC RANDOM Illumina HiSeq 2000 SRX3644452 FLOR11 SRP132090 PRJNA431782 Leaf or flower samples, were grounded to fine powder. According to the manufacturers protocols, total RNAs were isolated using the Trizol reagent followed by treatment with RNase-free DNase I. The quality of RNAs was checked using Agilent 2100 Bioanalyzer. RNA-Seq libraries were prepared and sequenced on the HiSeq 2000 system, following the manufacturer s instructions. SRS2909244 SAMN08405648 FLOR11 RNA-Seq TRANSCRIPTOMIC RANDOM Illumina HiSeq 2000