PRJDB6135 SAMD00089594 hm1_RNAseq RNA-Seq TRANSCRIPTOMIC PolyA R. irregularis DAOM181602 was axenically cultured on modified M medium at 28????????????????C for 42 days. 20 germ tubes were dissected from spores and sampled. RNA was extracted by using NucleoSpin RNA XS kit (MACGEREY-NAGEL) with RNase-Free DNase Set (Qiagen). RNA was reverse-transcribed and amplified by using SMART-Seq v4 kit. cDNA quality and quantity were checked by using Agilent 2100 Bioanalyzer. cDNA was sheared by using Coveris S2 system and transformed to illumina libraries by using Low imput library prep kit (Chlontec). After the quality and quantity were confirmed by using Agilent 2100 Bioanalyzer and KAPA Library quantification kit, the libraries were sequenced by HiSeq 1500. 126 0 Application Read Forward 1 Illumina HiSeq 1500 PRJDB6135 SAMD00089595 hm2_RNAseq RNA-Seq TRANSCRIPTOMIC PolyA R. irregularis DAOM181602 was axenically cultured on modified M medium at 28????????????????C for 42 days. 20 germ tubes were dissected from spores and sampled. RNA was extracted by using NucleoSpin RNA XS kit (MACGEREY-NAGEL) with RNase-Free DNase Set (Qiagen). RNA was reverse-transcribed and amplified by using SMART-Seq v4 kit. cDNA quality and quantity were checked by using Agilent 2100 Bioanalyzer. cDNA was sheared by using Coveris S2 system and transformed to illumina libraries by using Low imput library prep kit (Chlontec). After the quality and quantity were confirmed by using Agilent 2100 Bioanalyzer and KAPA Library quantification kit, the libraries were sequenced by HiSeq 1500. 126 0 Application Read Forward 1 Illumina HiSeq 1500 PRJDB6135 SAMD00089596 hm3_RNAseq RNA-Seq TRANSCRIPTOMIC PolyA R. irregularis DAOM181602 was axenically cultured on modified M medium at 28????????????????C for 42 days. 20 germ tubes were dissected from spores and sampled. RNA was extracted by using NucleoSpin RNA XS kit (MACGEREY-NAGEL) with RNase-Free DNase Set (Qiagen). RNA was reverse-transcribed and amplified by using SMART-Seq v4 kit. cDNA quality and quantity were checked by using Agilent 2100 Bioanalyzer. cDNA was sheared by using Coveris S2 system and transformed to illumina libraries by using Low imput library prep kit (Chlontec). After the quality and quantity were confirmed by using Agilent 2100 Bioanalyzer and KAPA Library quantification kit, the libraries were sequenced by HiSeq 1500. 126 0 Application Read Forward 1 Illumina HiSeq 1500 PRJDB6135 SAMD00089597 hp1_RNAseq RNA-Seq TRANSCRIPTOMIC PolyA R. irregularis DAOM181602 was axenically cultured on modified M medium with 100 ????????????????????????M palmitoleic acid at 28????????????????C for 42 days. 20 germ tubes were dissected from spores and sampled. RNA was extracted by using NucleoSpin RNA XS kit (MACGEREY-NAGEL) with RNase-Free DNase Set (Qiagen). RNA was reverse-transcribed and amplified by using SMART-Seq v4 kit. cDNA quality and quantity were checked by using Agilent 2100 Bioanalyzer. cDNA was sheared by using Coveris S2 system and transformed to illumina libraries by using Low imput library prep kit (Chlontec). After the quality and quantity were confirmed by using Agilent 2100 Bioanalyzer and KAPA Library quantification kit, the libraries were sequenced by HiSeq 1500. 126 0 Application Read Forward 1 Illumina HiSeq 1500 PRJDB6135 SAMD00089598 hp2_RNAseq RNA-Seq TRANSCRIPTOMIC PolyA R. irregularis DAOM181602 was axenically cultured on modified M medium with 100 ????????????????????????M palmitoleic acid at 28????????????????C for 42 days. 20 germ tubes were dissected from spores and sampled. RNA was extracted by using NucleoSpin RNA XS kit (MACGEREY-NAGEL) with RNase-Free DNase Set (Qiagen). RNA was reverse-transcribed and amplified by using SMART-Seq v4 kit. cDNA quality and quantity were checked by using Agilent 2100 Bioanalyzer. cDNA was sheared by using Coveris S2 system and transformed to illumina libraries by using Low imput library prep kit (Chlontec). After the quality and quantity were confirmed by using Agilent 2100 Bioanalyzer and KAPA Library quantification kit, the libraries were sequenced by HiSeq 1500. 126 0 Application Read Forward 1 Illumina HiSeq 1500 PRJDB6135 SAMD00089599 hp3_RNAseq RNA-Seq TRANSCRIPTOMIC PolyA R. irregularis DAOM181602 was axenically cultured on modified M medium with 100 ????????????????????????M palmitoleic acid at 28????????????????C for 42 days. 20 germ tubes were dissected from spores and sampled. RNA was extracted by using NucleoSpin RNA XS kit (MACGEREY-NAGEL) with RNase-Free DNase Set (Qiagen). RNA was reverse-transcribed and amplified by using SMART-Seq v4 kit. cDNA quality and quantity were checked by using Agilent 2100 Bioanalyzer. cDNA was sheared by using Coveris S2 system and transformed to illumina libraries by using Low imput library prep kit (Chlontec). After the quality and quantity were confirmed by using Agilent 2100 Bioanalyzer and KAPA Library quantification kit, the libraries were sequenced by HiSeq 1500. 126 0 Application Read Forward 1 Illumina HiSeq 1500 PRJDB6135 SAMD00089600 sm1_RNAseq RNA-Seq TRANSCRIPTOMIC PolyA R. irregularis DAOM181602 was axenically cultured on modified M medium at 28????????????????C for 42 days. 20 spores were dissected from germ tubes and sampled. RNA was extracted by using NucleoSpin RNA XS kit (MACGEREY-NAGEL) with RNase-Free DNase Set (Qiagen). RNA was reverse-transcribed and amplified by using SMART-Seq v4 kit. cDNA quality and quantity were checked by using Agilent 2100 Bioanalyzer. cDNA was sheared by using Coveris S2 system and transformed to illumina libraries by using Low imput library prep kit (Chlontec). After the quality and quantity were confirmed by using Agilent 2100 Bioanalyzer and KAPA Library quantification kit, the libraries were sequenced by HiSeq 1500. 126 0 Application Read Forward 1 Illumina HiSeq 1500 PRJDB6135 SAMD00089601 sm2_RNAseq RNA-Seq TRANSCRIPTOMIC PolyA R. irregularis DAOM181602 was axenically cultured on modified M medium at 28????????????????C for 42 days. 20 spores were dissected from germ tubes and sampled. RNA was extracted by using NucleoSpin RNA XS kit (MACGEREY-NAGEL) with RNase-Free DNase Set (Qiagen). RNA was reverse-transcribed and amplified by using SMART-Seq v4 kit. cDNA quality and quantity were checked by using Agilent 2100 Bioanalyzer. cDNA was sheared by using Coveris S2 system and transformed to illumina libraries by using Low imput library prep kit (Chlontec). After the quality and quantity were confirmed by using Agilent 2100 Bioanalyzer and KAPA Library quantification kit, the libraries were sequenced by HiSeq 1500. 126 0 Application Read Forward 1 Illumina HiSeq 1500 PRJDB6135 SAMD00089602 sm3_RNAseq RNA-Seq TRANSCRIPTOMIC PolyA R. irregularis DAOM181602 was axenically cultured on modified M medium at 28????????????????C for 42 days. 20 spores were dissected from germ tubes and sampled. RNA was extracted by using NucleoSpin RNA XS kit (MACGEREY-NAGEL) with RNase-Free DNase Set (Qiagen). RNA was reverse-transcribed and amplified by using SMART-Seq v4 kit. cDNA quality and quantity were checked by using Agilent 2100 Bioanalyzer. cDNA was sheared by using Coveris S2 system and transformed to illumina libraries by using Low imput library prep kit (Chlontec). After the quality and quantity were confirmed by using Agilent 2100 Bioanalyzer and KAPA Library quantification kit, the libraries were sequenced by HiSeq 1500. 126 0 Application Read Forward 1 Illumina HiSeq 1500 PRJDB6135 SAMD00089603 sp1_RNAseq RNA-Seq TRANSCRIPTOMIC PolyA R. irregularis DAOM181602 was axenically cultured on modified M medium with 100 ????????????????????????M palmitoleic acid at 28????????????????C for 42 days. 20 spores were dissected from germ tubes and sampled. RNA was extracted by using NucleoSpin RNA XS kit (MACGEREY-NAGEL) with RNase-Free DNase Set (Qiagen). RNA was reverse-transcribed and amplified by using SMART-Seq v4 kit. cDNA quality and quantity were checked by using Agilent 2100 Bioanalyzer. cDNA was sheared by using Coveris S2 system and transformed to illumina libraries by using Low imput library prep kit (Chlontec). After the quality and quantity were confirmed by using Agilent 2100 Bioanalyzer and KAPA Library quantification kit, the libraries were sequenced by HiSeq 1500. 126 0 Application Read Forward 1 Illumina HiSeq 1500 PRJDB6135 SAMD00089604 sp2_RNAseq RNA-Seq TRANSCRIPTOMIC PolyA R. irregularis DAOM181602 was axenically cultured on modified M medium with 100 ????????????????????????M palmitoleic acid at 28????????????????C for 42 days. 20 spores were dissected from germ tubes and sampled. RNA was extracted by using NucleoSpin RNA XS kit (MACGEREY-NAGEL) with RNase-Free DNase Set (Qiagen). RNA was reverse-transcribed and amplified by using SMART-Seq v4 kit. cDNA quality and quantity were checked by using Agilent 2100 Bioanalyzer. cDNA was sheared by using Coveris S2 system and transformed to illumina libraries by using Low imput library prep kit (Chlontec). After the quality and quantity were confirmed by using Agilent 2100 Bioanalyzer and KAPA Library quantification kit, the libraries were sequenced by HiSeq 1500. 126 0 Application Read Forward 1 Illumina HiSeq 1500 PRJDB6135 SAMD00089605 sp3_RNAseq RNA-Seq TRANSCRIPTOMIC PolyA R. irregularis DAOM181602 was axenically cultured on modified M medium with 100 ????????????????????????M palmitoleic acid at 28????????????????C for 42 days. 20 spores were dissected from germ tubes and sampled. RNA was extracted by using NucleoSpin RNA XS kit (MACGEREY-NAGEL) with RNase-Free DNase Set (Qiagen). RNA was reverse-transcribed and amplified by using SMART-Seq v4 kit. cDNA quality and quantity were checked by using Agilent 2100 Bioanalyzer. cDNA was sheared by using Coveris S2 system and transformed to illumina libraries by using Low imput library prep kit (Chlontec). After the quality and quantity were confirmed by using Agilent 2100 Bioanalyzer and KAPA Library quantification kit, the libraries were sequenced by HiSeq 1500. 126 0 Application Read Forward 1 Illumina HiSeq 1500