GSM2794936: CS12_B_1_1; Vitis vinifera; RNA-Seq

SRX3219235 GSM2794936 GSM2794936: CS12_B_1_1; Vitis vinifera; RNA-Seq SRP118973 SRS2543919 GSM2794936 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794936 GSM2794936 GEO Accession GSM2794936 SRX3219236 GSM2794937 GSM2794937: CS12_B_2_1; Vitis vinifera; RNA-Seq SRP118973 SRS2543920 GSM2794937 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794937 GSM2794937 GEO Accession GSM2794937 SRX3219237 GSM2794938 GSM2794938: CS12_B_3_1; Vitis vinifera; RNA-Seq SRP118973 SRS2543922 GSM2794938 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794938 GSM2794938 GEO Accession GSM2794938 SRX3219238 GSM2794939 GSM2794939: CS12_C_1_1; Vitis vinifera; RNA-Seq SRP118973 SRS2543921 GSM2794939 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794939 GSM2794939 GEO Accession GSM2794939 SRX3219239 GSM2794940 GSM2794940: CS12_C_2_1; Vitis vinifera; RNA-Seq SRP118973 SRS2543923 GSM2794940 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794940 GSM2794940 GEO Accession GSM2794940 SRX3219240 GSM2794941 GSM2794941: CS12_C_3_1; Vitis vinifera; RNA-Seq SRP118973 SRS2543924 GSM2794941 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794941 GSM2794941 GEO Accession GSM2794941 SRX3219241 GSM2794942 GSM2794942: CS12_B_1_2; Vitis vinifera; RNA-Seq SRP118973 SRS2543925 GSM2794942 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794942 GSM2794942 GEO Accession GSM2794942 SRX3219242 GSM2794943 GSM2794943: CS12_B_2_2; Vitis vinifera; RNA-Seq SRP118973 SRS2543926 GSM2794943 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794943 GSM2794943 GEO Accession GSM2794943 SRX3219243 GSM2794944 GSM2794944: CS12_B_3_2; Vitis vinifera; RNA-Seq SRP118973 SRS2543927 GSM2794944 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794944 GSM2794944 GEO Accession GSM2794944 SRX3219244 GSM2794945 GSM2794945: CS12_C_1_2; Vitis vinifera; RNA-Seq SRP118973 SRS2543928 GSM2794945 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794945 GSM2794945 GEO Accession GSM2794945 SRX3219245 GSM2794946 GSM2794946: CS12_C_2_2; Vitis vinifera; RNA-Seq SRP118973 SRS2543929 GSM2794946 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794946 GSM2794946 GEO Accession GSM2794946 SRX3219246 GSM2794947 GSM2794947: CS12_C_3_2; Vitis vinifera; RNA-Seq SRP118973 SRS2543931 GSM2794947 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794947 GSM2794947 GEO Accession GSM2794947 SRX3219247 GSM2794948 GSM2794948: CS12_B_1_3; Vitis vinifera; RNA-Seq SRP118973 SRS2543930 GSM2794948 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794948 GSM2794948 GEO Accession GSM2794948 SRX3219248 GSM2794949 GSM2794949: CS12_B_2_3; Vitis vinifera; RNA-Seq SRP118973 SRS2543934 GSM2794949 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794949 GSM2794949 GEO Accession GSM2794949 SRX3219249 GSM2794950 GSM2794950: CS12_B_3_3; Vitis vinifera; RNA-Seq SRP118973 SRS2543932 GSM2794950 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794950 GSM2794950 GEO Accession GSM2794950 SRX3219250 GSM2794951 GSM2794951: CS12_C_1_3; Vitis vinifera; RNA-Seq SRP118973 SRS2543933 GSM2794951 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794951 GSM2794951 GEO Accession GSM2794951 SRX3219251 GSM2794952 GSM2794952: CS12_C_2_3; Vitis vinifera; RNA-Seq SRP118973 SRS2543935 GSM2794952 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794952 GSM2794952 GEO Accession GSM2794952 SRX3219252 GSM2794953 GSM2794953: CS12_C_3_3; Vitis vinifera; RNA-Seq SRP118973 SRS2543936 GSM2794953 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794953 GSM2794953 GEO Accession GSM2794953 SRX3219253 GSM2794954 GSM2794954: CS12_B_1_4; Vitis vinifera; RNA-Seq SRP118973 SRS2543978 GSM2794954 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794954 GSM2794954 GEO Accession GSM2794954 SRX3219254 GSM2794955 GSM2794955: CS12_B_2_4; Vitis vinifera; RNA-Seq SRP118973 SRS2543937 GSM2794955 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794955 GSM2794955 GEO Accession GSM2794955 SRX3219255 GSM2794956 GSM2794956: CS12_B_3_4; Vitis vinifera; RNA-Seq SRP118973 SRS2543938 GSM2794956 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794956 GSM2794956 GEO Accession GSM2794956 SRX3219256 GSM2794957 GSM2794957: CS12_C_1_4; Vitis vinifera; RNA-Seq SRP118973 SRS2543939 GSM2794957 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794957 GSM2794957 GEO Accession GSM2794957 SRX3219257 GSM2794958 GSM2794958: CS12_C_2_4; Vitis vinifera; RNA-Seq SRP118973 SRS2543940 GSM2794958 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794958 GSM2794958 GEO Accession GSM2794958 SRX3219258 GSM2794959 GSM2794959: CS12_C_3_4; Vitis vinifera; RNA-Seq SRP118973 SRS2543941 GSM2794959 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794959 GSM2794959 GEO Accession GSM2794959 SRX3219259 GSM2794960 GSM2794960: CS12_B_1_5; Vitis vinifera; RNA-Seq SRP118973 SRS2543942 GSM2794960 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794960 GSM2794960 GEO Accession GSM2794960 SRX3219260 GSM2794961 GSM2794961: CS12_B_2_5; Vitis vinifera; RNA-Seq SRP118973 SRS2543943 GSM2794961 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794961 GSM2794961 GEO Accession GSM2794961 SRX3219261 GSM2794962 GSM2794962: CS12_B_3_5; Vitis vinifera; RNA-Seq SRP118973 SRS2543944 GSM2794962 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794962 GSM2794962 GEO Accession GSM2794962 SRX3219262 GSM2794963 GSM2794963: CS12_C_1_5; Vitis vinifera; RNA-Seq SRP118973 SRS2543945 GSM2794963 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794963 GSM2794963 GEO Accession GSM2794963 SRX3219263 GSM2794964 GSM2794964: CS12_C_2_5; Vitis vinifera; RNA-Seq SRP118973 SRS2543946 GSM2794964 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794964 GSM2794964 GEO Accession GSM2794964 SRX3219264 GSM2794965 GSM2794965: CS12_C_3_5; Vitis vinifera; RNA-Seq SRP118973 SRS2543947 GSM2794965 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794965 GSM2794965 GEO Accession GSM2794965 SRX3219265 GSM2794966 GSM2794966: CS12_B_1_6; Vitis vinifera; RNA-Seq SRP118973 SRS2543948 GSM2794966 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794966 GSM2794966 GEO Accession GSM2794966 SRX3219266 GSM2794967 GSM2794967: CS12_B_2_6; Vitis vinifera; RNA-Seq SRP118973 SRS2543998 GSM2794967 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794967 GSM2794967 GEO Accession GSM2794967 SRX3219267 GSM2794968 GSM2794968: CS12_B_3_6; Vitis vinifera; RNA-Seq SRP118973 SRS2543949 GSM2794968 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794968 GSM2794968 GEO Accession GSM2794968 SRX3219268 GSM2794969 GSM2794969: CS12_C_1_6; Vitis vinifera; RNA-Seq SRP118973 SRS2543950 GSM2794969 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794969 GSM2794969 GEO Accession GSM2794969 SRX3219269 GSM2794970 GSM2794970: CS12_C_2_6; Vitis vinifera; RNA-Seq SRP118973 SRS2543952 GSM2794970 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794970 GSM2794970 GEO Accession GSM2794970 SRX3219270 GSM2794971 GSM2794971: CS12_C_3_6; Vitis vinifera; RNA-Seq SRP118973 SRS2543951 GSM2794971 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794971 GSM2794971 GEO Accession GSM2794971 SRX3219271 GSM2794972 GSM2794972: CS12_B_1_7; Vitis vinifera; RNA-Seq SRP118973 SRS2543953 GSM2794972 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794972 GSM2794972 GEO Accession GSM2794972 SRX3219272 GSM2794973 GSM2794973: CS12_B_2_7; Vitis vinifera; RNA-Seq SRP118973 SRS2543955 GSM2794973 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794973 GSM2794973 GEO Accession GSM2794973 SRX3219273 GSM2794974 GSM2794974: CS12_B_3_7; Vitis vinifera; RNA-Seq SRP118973 SRS2543954 GSM2794974 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794974 GSM2794974 GEO Accession GSM2794974 SRX3219274 GSM2794975 GSM2794975: CS12_C_1_7; Vitis vinifera; RNA-Seq SRP118973 SRS2544013 GSM2794975 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794975 GSM2794975 GEO Accession GSM2794975 SRX3219275 GSM2794976 GSM2794976: CS12_C_2_7; Vitis vinifera; RNA-Seq SRP118973 SRS2543956 GSM2794976 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794976 GSM2794976 GEO Accession GSM2794976 SRX3219276 GSM2794977 GSM2794977: CS12_C_3_7; Vitis vinifera; RNA-Seq SRP118973 SRS2543957 GSM2794977 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794977 GSM2794977 GEO Accession GSM2794977 SRX3219277 GSM2794978 GSM2794978: CS12_B_1_8; Vitis vinifera; RNA-Seq SRP118973 SRS2543958 GSM2794978 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794978 GSM2794978 GEO Accession GSM2794978 SRX3219278 GSM2794979 GSM2794979: CS12_B_2_8; Vitis vinifera; RNA-Seq SRP118973 SRS2543959 GSM2794979 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794979 GSM2794979 GEO Accession GSM2794979 SRX3219279 GSM2794980 GSM2794980: CS12_B_3_8; Vitis vinifera; RNA-Seq SRP118973 SRS2543960 GSM2794980 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794980 GSM2794980 GEO Accession GSM2794980 SRX3219280 GSM2794981 GSM2794981: CS12_C_1_8; Vitis vinifera; RNA-Seq SRP118973 SRS2543961 GSM2794981 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794981 GSM2794981 GEO Accession GSM2794981 SRX3219281 GSM2794982 GSM2794982: CS12_C_2_8; Vitis vinifera; RNA-Seq SRP118973 SRS2543962 GSM2794982 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794982 GSM2794982 GEO Accession GSM2794982 SRX3219282 GSM2794983 GSM2794983: CS12_C_3_8; Vitis vinifera; RNA-Seq SRP118973 SRS2543963 GSM2794983 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794983 GSM2794983 GEO Accession GSM2794983 SRX3219283 GSM2794984 GSM2794984: CS12_B_1_9; Vitis vinifera; RNA-Seq SRP118973 SRS2544014 GSM2794984 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794984 GSM2794984 GEO Accession GSM2794984 SRX3219284 GSM2794985 GSM2794985: CS12_B_2_9; Vitis vinifera; RNA-Seq SRP118973 SRS2543964 GSM2794985 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794985 GSM2794985 GEO Accession GSM2794985 SRX3219285 GSM2794986 GSM2794986: CS12_B_3_9; Vitis vinifera; RNA-Seq SRP118973 SRS2543965 GSM2794986 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794986 GSM2794986 GEO Accession GSM2794986 SRX3219286 GSM2794987 GSM2794987: CS12_C_1_9; Vitis vinifera; RNA-Seq SRP118973 SRS2543966 GSM2794987 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794987 GSM2794987 GEO Accession GSM2794987 SRX3219287 GSM2794988 GSM2794988: CS12_C_2_9; Vitis vinifera; RNA-Seq SRP118973 SRS2543967 GSM2794988 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794988 GSM2794988 GEO Accession GSM2794988 SRX3219288 GSM2794989 GSM2794989: CS12_C_3_9; Vitis vinifera; RNA-Seq SRP118973 SRS2543968 GSM2794989 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794989 GSM2794989 GEO Accession GSM2794989 SRX3219289 GSM2794990 GSM2794990: CS12_B_1_10; Vitis vinifera; RNA-Seq SRP118973 SRS2543969 GSM2794990 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794990 GSM2794990 GEO Accession GSM2794990 SRX3219290 GSM2794991 GSM2794991: CS12_B_2_10; Vitis vinifera; RNA-Seq SRP118973 SRS2543970 GSM2794991 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794991 GSM2794991 GEO Accession GSM2794991 SRX3219291 GSM2794992 GSM2794992: CS12_B_3_10; Vitis vinifera; RNA-Seq SRP118973 SRS2543971 GSM2794992 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794992 GSM2794992 GEO Accession GSM2794992 SRX3219292 GSM2794993 GSM2794993: CS12_C_1_10; Vitis vinifera; RNA-Seq SRP118973 SRS2543972 GSM2794993 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794993 GSM2794993 GEO Accession GSM2794993 SRX3219293 GSM2794994 GSM2794994: CS12_C_2_10; Vitis vinifera; RNA-Seq SRP118973 SRS2543973 GSM2794994 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794994 GSM2794994 GEO Accession GSM2794994 SRX3219294 GSM2794995 GSM2794995: CS12_C_3_10; Vitis vinifera; RNA-Seq SRP118973 SRS2543974 GSM2794995 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794995 GSM2794995 GEO Accession GSM2794995 SRX3219295 GSM2794996 GSM2794996: CS12_B_1_11; Vitis vinifera; RNA-Seq SRP118973 SRS2543975 GSM2794996 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794996 GSM2794996 GEO Accession GSM2794996 SRX3219296 GSM2794997 GSM2794997: CS12_B_2_11; Vitis vinifera; RNA-Seq SRP118973 SRS2543976 GSM2794997 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794997 GSM2794997 GEO Accession GSM2794997 SRX3219297 GSM2794998 GSM2794998: CS12_B_3_11; Vitis vinifera; RNA-Seq SRP118973 SRS2543977 GSM2794998 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794998 GSM2794998 GEO Accession GSM2794998 SRX3219298 GSM2794999 GSM2794999: CS12_C_1_11; Vitis vinifera; RNA-Seq SRP118973 SRS2543979 GSM2794999 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302794999 GSM2794999 GEO Accession GSM2794999 SRX3219299 GSM2795000 GSM2795000: CS12_C_2_11; Vitis vinifera; RNA-Seq SRP118973 SRS2543980 GSM2795000 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795000 GSM2795000 GEO Accession GSM2795000 SRX3219300 GSM2795001 GSM2795001: CS12_C_3_11; Vitis vinifera; RNA-Seq SRP118973 SRS2543981 GSM2795001 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795001 GSM2795001 GEO Accession GSM2795001 SRX3219301 GSM2795002 GSM2795002: CS12_B_1_12; Vitis vinifera; RNA-Seq SRP118973 SRS2543982 GSM2795002 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795002 GSM2795002 GEO Accession GSM2795002 SRX3219302 GSM2795003 GSM2795003: CS12_B_2_12; Vitis vinifera; RNA-Seq SRP118973 SRS2543983 GSM2795003 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795003 GSM2795003 GEO Accession GSM2795003 SRX3219303 GSM2795004 GSM2795004: CS12_B_3_12; Vitis vinifera; RNA-Seq SRP118973 SRS2543984 GSM2795004 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795004 GSM2795004 GEO Accession GSM2795004 SRX3219304 GSM2795005 GSM2795005: CS12_C_1_12; Vitis vinifera; RNA-Seq SRP118973 SRS2543985 GSM2795005 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795005 GSM2795005 GEO Accession GSM2795005 SRX3219305 GSM2795006 GSM2795006: CS12_C_2_12; Vitis vinifera; RNA-Seq SRP118973 SRS2543986 GSM2795006 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795006 GSM2795006 GEO Accession GSM2795006 SRX3219306 GSM2795007 GSM2795007: CS12_C_3_12; Vitis vinifera; RNA-Seq SRP118973 SRS2543987 GSM2795007 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795007 GSM2795007 GEO Accession GSM2795007 SRX3219307 GSM2795008 GSM2795008: CS13_B_1_1; Vitis vinifera; RNA-Seq SRP118973 SRS2543988 GSM2795008 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795008 GSM2795008 GEO Accession GSM2795008 SRX3219308 GSM2795009 GSM2795009: CS13_B_2_1; Vitis vinifera; RNA-Seq SRP118973 SRS2543989 GSM2795009 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795009 GSM2795009 GEO Accession GSM2795009 SRX3219309 GSM2795010 GSM2795010: CS13_B_3_1; Vitis vinifera; RNA-Seq SRP118973 SRS2543990 GSM2795010 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795010 GSM2795010 GEO Accession GSM2795010 SRX3219310 GSM2795011 GSM2795011: CS13_C_1_1; Vitis vinifera; RNA-Seq SRP118973 SRS2543991 GSM2795011 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795011 GSM2795011 GEO Accession GSM2795011 SRX3219311 GSM2795012 GSM2795012: CS13_C_2_1; Vitis vinifera; RNA-Seq SRP118973 SRS2543992 GSM2795012 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795012 GSM2795012 GEO Accession GSM2795012 SRX3219312 GSM2795013 GSM2795013: CS13_C_3_1; Vitis vinifera; RNA-Seq SRP118973 SRS2543993 GSM2795013 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795013 GSM2795013 GEO Accession GSM2795013 SRX3219313 GSM2795014 GSM2795014: CS13_B_1_2; Vitis vinifera; RNA-Seq SRP118973 SRS2543994 GSM2795014 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795014 GSM2795014 GEO Accession GSM2795014 SRX3219314 GSM2795015 GSM2795015: CS13_B_2_2; Vitis vinifera; RNA-Seq SRP118973 SRS2543995 GSM2795015 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795015 GSM2795015 GEO Accession GSM2795015 SRX3219315 GSM2795016 GSM2795016: CS13_B_3_2; Vitis vinifera; RNA-Seq SRP118973 SRS2543996 GSM2795016 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795016 GSM2795016 GEO Accession GSM2795016 SRX3219316 GSM2795017 GSM2795017: CS13_C_1_2; Vitis vinifera; RNA-Seq SRP118973 SRS2543997 GSM2795017 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795017 GSM2795017 GEO Accession GSM2795017 SRX3219317 GSM2795018 GSM2795018: CS13_C_2_2; Vitis vinifera; RNA-Seq SRP118973 SRS2543999 GSM2795018 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795018 GSM2795018 GEO Accession GSM2795018 SRX3219318 GSM2795019 GSM2795019: CS13_C_3_2; Vitis vinifera; RNA-Seq SRP118973 SRS2544000 GSM2795019 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795019 GSM2795019 GEO Accession GSM2795019 SRX3219319 GSM2795020 GSM2795020: CS13_B_1_3; Vitis vinifera; RNA-Seq SRP118973 SRS2544001 GSM2795020 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795020 GSM2795020 GEO Accession GSM2795020 SRX3219320 GSM2795021 GSM2795021: CS13_B_2_3; Vitis vinifera; RNA-Seq SRP118973 SRS2544002 GSM2795021 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795021 GSM2795021 GEO Accession GSM2795021 SRX3219321 GSM2795022 GSM2795022: CS13_B_3_3; Vitis vinifera; RNA-Seq SRP118973 SRS2544003 GSM2795022 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795022 GSM2795022 GEO Accession GSM2795022 SRX3219322 GSM2795023 GSM2795023: CS13_C_1_3; Vitis vinifera; RNA-Seq SRP118973 SRS2544004 GSM2795023 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795023 GSM2795023 GEO Accession GSM2795023 SRX3219323 GSM2795024 GSM2795024: CS13_C_2_3; Vitis vinifera; RNA-Seq SRP118973 SRS2544005 GSM2795024 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795024 GSM2795024 GEO Accession GSM2795024 SRX3219324 GSM2795025 GSM2795025: CS13_C_3_3; Vitis vinifera; RNA-Seq SRP118973 SRS2544006 GSM2795025 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795025 GSM2795025 GEO Accession GSM2795025 SRX3219325 GSM2795026 GSM2795026: CS13_B_1_4; Vitis vinifera; RNA-Seq SRP118973 SRS2544007 GSM2795026 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795026 GSM2795026 GEO Accession GSM2795026 SRX3219326 GSM2795027 GSM2795027: CS13_B_2_4; Vitis vinifera; RNA-Seq SRP118973 SRS2544008 GSM2795027 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795027 GSM2795027 GEO Accession GSM2795027 SRX3219327 GSM2795028 GSM2795028: CS13_B_3_4; Vitis vinifera; RNA-Seq SRP118973 SRS2544009 GSM2795028 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795028 GSM2795028 GEO Accession GSM2795028 SRX3219328 GSM2795029 GSM2795029: CS13_C_1_4; Vitis vinifera; RNA-Seq SRP118973 SRS2544121 GSM2795029 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795029 GSM2795029 GEO Accession GSM2795029 SRX3219329 GSM2795030 GSM2795030: CS13_C_2_4; Vitis vinifera; RNA-Seq SRP118973 SRS2544010 GSM2795030 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795030 GSM2795030 GEO Accession GSM2795030 SRX3219330 GSM2795031 GSM2795031: CS13_C_3_4; Vitis vinifera; RNA-Seq SRP118973 SRS2544011 GSM2795031 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795031 GSM2795031 GEO Accession GSM2795031 SRX3219331 GSM2795032 GSM2795032: CS13_B_1_5; Vitis vinifera; RNA-Seq SRP118973 SRS2544012 GSM2795032 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795032 GSM2795032 GEO Accession GSM2795032 SRX3219332 GSM2795033 GSM2795033: CS13_B_2_5; Vitis vinifera; RNA-Seq SRP118973 SRS2544015 GSM2795033 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795033 GSM2795033 GEO Accession GSM2795033 SRX3219333 GSM2795034 GSM2795034: CS13_B_3_5; Vitis vinifera; RNA-Seq SRP118973 SRS2544016 GSM2795034 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795034 GSM2795034 GEO Accession GSM2795034 SRX3219334 GSM2795035 GSM2795035: CS13_C_1_5; Vitis vinifera; RNA-Seq SRP118973 SRS2544017 GSM2795035 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795035 GSM2795035 GEO Accession GSM2795035 SRX3219335 GSM2795036 GSM2795036: CS13_C_2_5; Vitis vinifera; RNA-Seq SRP118973 SRS2544018 GSM2795036 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795036 GSM2795036 GEO Accession GSM2795036 SRX3219336 GSM2795037 GSM2795037: CS13_C_3_5; Vitis vinifera; RNA-Seq SRP118973 SRS2544019 GSM2795037 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795037 GSM2795037 GEO Accession GSM2795037 SRX3219337 GSM2795038 GSM2795038: CS13_B_1_6; Vitis vinifera; RNA-Seq SRP118973 SRS2544020 GSM2795038 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795038 GSM2795038 GEO Accession GSM2795038 SRX3219338 GSM2795039 GSM2795039: CS13_B_2_6; Vitis vinifera; RNA-Seq SRP118973 SRS2544021 GSM2795039 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795039 GSM2795039 GEO Accession GSM2795039 SRX3219339 GSM2795040 GSM2795040: CS13_B_3_6; Vitis vinifera; RNA-Seq SRP118973 SRS2544023 GSM2795040 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795040 GSM2795040 GEO Accession GSM2795040 SRX3219340 GSM2795041 GSM2795041: CS13_C_1_6; Vitis vinifera; RNA-Seq SRP118973 SRS2544024 GSM2795041 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795041 GSM2795041 GEO Accession GSM2795041 SRX3219341 GSM2795042 GSM2795042: CS13_C_2_6; Vitis vinifera; RNA-Seq SRP118973 SRS2544022 GSM2795042 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795042 GSM2795042 GEO Accession GSM2795042 SRX3219342 GSM2795043 GSM2795043: CS13_C_3_6; Vitis vinifera; RNA-Seq SRP118973 SRS2544025 GSM2795043 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795043 GSM2795043 GEO Accession GSM2795043 SRX3219343 GSM2795044 GSM2795044: CS13_B_1_7; Vitis vinifera; RNA-Seq SRP118973 SRS2544026 GSM2795044 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795044 GSM2795044 GEO Accession GSM2795044 SRX3219344 GSM2795045 GSM2795045: CS13_B_2_7; Vitis vinifera; RNA-Seq SRP118973 SRS2544028 GSM2795045 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795045 GSM2795045 GEO Accession GSM2795045 SRX3219345 GSM2795046 GSM2795046: CS13_B_3_7; Vitis vinifera; RNA-Seq SRP118973 SRS2544027 GSM2795046 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795046 GSM2795046 GEO Accession GSM2795046 SRX3219346 GSM2795047 GSM2795047: CS13_C_1_7; Vitis vinifera; RNA-Seq SRP118973 SRS2544029 GSM2795047 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795047 GSM2795047 GEO Accession GSM2795047 SRX3219347 GSM2795048 GSM2795048: CS13_C_2_7; Vitis vinifera; RNA-Seq SRP118973 SRS2544031 GSM2795048 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795048 GSM2795048 GEO Accession GSM2795048 SRX3219348 GSM2795049 GSM2795049: CS13_C_3_7; Vitis vinifera; RNA-Seq SRP118973 SRS2544033 GSM2795049 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795049 GSM2795049 GEO Accession GSM2795049 SRX3219349 GSM2795050 GSM2795050: CS13_B_1_8; Vitis vinifera; RNA-Seq SRP118973 SRS2544032 GSM2795050 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795050 GSM2795050 GEO Accession GSM2795050 SRX3219350 GSM2795051 GSM2795051: CS13_B_2_8; Vitis vinifera; RNA-Seq SRP118973 SRS2544030 GSM2795051 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795051 GSM2795051 GEO Accession GSM2795051 SRX3219351 GSM2795052 GSM2795052: CS13_B_3_8; Vitis vinifera; RNA-Seq SRP118973 SRS2544034 GSM2795052 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795052 GSM2795052 GEO Accession GSM2795052 SRX3219352 GSM2795053 GSM2795053: CS13_C_1_8; Vitis vinifera; RNA-Seq SRP118973 SRS2544036 GSM2795053 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795053 GSM2795053 GEO Accession GSM2795053 SRX3219353 GSM2795054 GSM2795054: CS13_C_2_8; Vitis vinifera; RNA-Seq SRP118973 SRS2544035 GSM2795054 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795054 GSM2795054 GEO Accession GSM2795054 SRX3219354 GSM2795055 GSM2795055: CS13_C_3_8; Vitis vinifera; RNA-Seq SRP118973 SRS2544037 GSM2795055 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795055 GSM2795055 GEO Accession GSM2795055 SRX3219355 GSM2795056 GSM2795056: CS13_B_1_9; Vitis vinifera; RNA-Seq SRP118973 SRS2544038 GSM2795056 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795056 GSM2795056 GEO Accession GSM2795056 SRX3219356 GSM2795057 GSM2795057: CS13_B_2_9; Vitis vinifera; RNA-Seq SRP118973 SRS2544039 GSM2795057 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795057 GSM2795057 GEO Accession GSM2795057 SRX3219357 GSM2795058 GSM2795058: CS13_B_3_9; Vitis vinifera; RNA-Seq SRP118973 SRS2544041 GSM2795058 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795058 GSM2795058 GEO Accession GSM2795058 SRX3219358 GSM2795059 GSM2795059: CS13_C_1_9; Vitis vinifera; RNA-Seq SRP118973 SRS2544040 GSM2795059 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795059 GSM2795059 GEO Accession GSM2795059 SRX3219359 GSM2795060 GSM2795060: CS13_C_2_9; Vitis vinifera; RNA-Seq SRP118973 SRS2544042 GSM2795060 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795060 GSM2795060 GEO Accession GSM2795060 SRX3219360 GSM2795061 GSM2795061: CS13_C_3_9; Vitis vinifera; RNA-Seq SRP118973 SRS2544043 GSM2795061 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795061 GSM2795061 GEO Accession GSM2795061 SRX3219361 GSM2795062 GSM2795062: CS13_B_1_10; Vitis vinifera; RNA-Seq SRP118973 SRS2544045 GSM2795062 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795062 GSM2795062 GEO Accession GSM2795062 SRX3219362 GSM2795063 GSM2795063: CS13_B_2_10; Vitis vinifera; RNA-Seq SRP118973 SRS2544044 GSM2795063 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795063 GSM2795063 GEO Accession GSM2795063 SRX3219363 GSM2795064 GSM2795064: CS13_B_3_10; Vitis vinifera; RNA-Seq SRP118973 SRS2544047 GSM2795064 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795064 GSM2795064 GEO Accession GSM2795064 SRX3219364 GSM2795065 GSM2795065: CS13_C_1_10; Vitis vinifera; RNA-Seq SRP118973 SRS2544046 GSM2795065 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795065 GSM2795065 GEO Accession GSM2795065 SRX3219365 GSM2795066 GSM2795066: CS13_C_2_10; Vitis vinifera; RNA-Seq SRP118973 SRS2544048 GSM2795066 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795066 GSM2795066 GEO Accession GSM2795066 SRX3219366 GSM2795067 GSM2795067: CS13_C_3_10; Vitis vinifera; RNA-Seq SRP118973 SRS2544049 GSM2795067 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795067 GSM2795067 GEO Accession GSM2795067 SRX3219367 GSM2795068 GSM2795068: CS14_B_1_1; Vitis vinifera; RNA-Seq SRP118973 SRS2544051 GSM2795068 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795068 GSM2795068 GEO Accession GSM2795068 SRX3219368 GSM2795069 GSM2795069: CS14_B_2_1; Vitis vinifera; RNA-Seq SRP118973 SRS2544052 GSM2795069 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795069 GSM2795069 GEO Accession GSM2795069 SRX3219369 GSM2795070 GSM2795070: CS14_B_3_1; Vitis vinifera; RNA-Seq SRP118973 SRS2544053 GSM2795070 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795070 GSM2795070 GEO Accession GSM2795070 SRX3219370 GSM2795071 GSM2795071: CS14_C_1_1; Vitis vinifera; RNA-Seq SRP118973 SRS2544050 GSM2795071 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795071 GSM2795071 GEO Accession GSM2795071 SRX3219371 GSM2795072 GSM2795072: CS14_C_2_1; Vitis vinifera; RNA-Seq SRP118973 SRS2544054 GSM2795072 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795072 GSM2795072 GEO Accession GSM2795072 SRX3219372 GSM2795073 GSM2795073: CS14_C_3_1; Vitis vinifera; RNA-Seq SRP118973 SRS2544055 GSM2795073 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795073 GSM2795073 GEO Accession GSM2795073 SRX3219373 GSM2795074 GSM2795074: CS14_B_1_2; Vitis vinifera; RNA-Seq SRP118973 SRS2544056 GSM2795074 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795074 GSM2795074 GEO Accession GSM2795074 SRX3219374 GSM2795075 GSM2795075: CS14_B_2_2; Vitis vinifera; RNA-Seq SRP118973 SRS2544057 GSM2795075 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795075 GSM2795075 GEO Accession GSM2795075 SRX3219375 GSM2795076 GSM2795076: CS14_B_3_2; Vitis vinifera; RNA-Seq SRP118973 SRS2544058 GSM2795076 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795076 GSM2795076 GEO Accession GSM2795076 SRX3219376 GSM2795077 GSM2795077: CS14_C_1_2; Vitis vinifera; RNA-Seq SRP118973 SRS2544059 GSM2795077 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795077 GSM2795077 GEO Accession GSM2795077 SRX3219377 GSM2795078 GSM2795078: CS14_C_2_2; Vitis vinifera; RNA-Seq SRP118973 SRS2544060 GSM2795078 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795078 GSM2795078 GEO Accession GSM2795078 SRX3219378 GSM2795079 GSM2795079: CS14_C_3_2; Vitis vinifera; RNA-Seq SRP118973 SRS2544062 GSM2795079 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795079 GSM2795079 GEO Accession GSM2795079 SRX3219379 GSM2795080 GSM2795080: CS14_B_1_3; Vitis vinifera; RNA-Seq SRP118973 SRS2544063 GSM2795080 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795080 GSM2795080 GEO Accession GSM2795080 SRX3219380 GSM2795081 GSM2795081: CS14_B_2_3; Vitis vinifera; RNA-Seq SRP118973 SRS2544061 GSM2795081 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795081 GSM2795081 GEO Accession GSM2795081 SRX3219381 GSM2795082 GSM2795082: CS14_B_3_3; Vitis vinifera; RNA-Seq SRP118973 SRS2544064 GSM2795082 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795082 GSM2795082 GEO Accession GSM2795082 SRX3219382 GSM2795083 GSM2795083: CS14_C_1_3; Vitis vinifera; RNA-Seq SRP118973 SRS2544122 GSM2795083 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795083 GSM2795083 GEO Accession GSM2795083 SRX3219383 GSM2795084 GSM2795084: CS14_C_2_3; Vitis vinifera; RNA-Seq SRP118973 SRS2544065 GSM2795084 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795084 GSM2795084 GEO Accession GSM2795084 SRX3219384 GSM2795085 GSM2795085: CS14_C_3_3; Vitis vinifera; RNA-Seq SRP118973 SRS2544066 GSM2795085 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795085 GSM2795085 GEO Accession GSM2795085 SRX3219385 GSM2795086 GSM2795086: CS14_B_1_4; Vitis vinifera; RNA-Seq SRP118973 SRS2544067 GSM2795086 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795086 GSM2795086 GEO Accession GSM2795086 SRX3219386 GSM2795087 GSM2795087: CS14_B_2_4; Vitis vinifera; RNA-Seq SRP118973 SRS2544068 GSM2795087 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795087 GSM2795087 GEO Accession GSM2795087 SRX3219387 GSM2795088 GSM2795088: CS14_B_3_4; Vitis vinifera; RNA-Seq SRP118973 SRS2544069 GSM2795088 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795088 GSM2795088 GEO Accession GSM2795088 SRX3219388 GSM2795089 GSM2795089: CS14_C_1_4; Vitis vinifera; RNA-Seq SRP118973 SRS2544070 GSM2795089 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795089 GSM2795089 GEO Accession GSM2795089 SRX3219389 GSM2795090 GSM2795090: CS14_C_2_4; Vitis vinifera; RNA-Seq SRP118973 SRS2544071 GSM2795090 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795090 GSM2795090 GEO Accession GSM2795090 SRX3219390 GSM2795091 GSM2795091: CS14_C_3_4; Vitis vinifera; RNA-Seq SRP118973 SRS2544072 GSM2795091 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795091 GSM2795091 GEO Accession GSM2795091 SRX3219391 GSM2795092 GSM2795092: CS14_B_1_5; Vitis vinifera; RNA-Seq SRP118973 SRS2544073 GSM2795092 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795092 GSM2795092 GEO Accession GSM2795092 SRX3219392 GSM2795093 GSM2795093: CS14_B_2_5; Vitis vinifera; RNA-Seq SRP118973 SRS2544074 GSM2795093 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795093 GSM2795093 GEO Accession GSM2795093 SRX3219393 GSM2795094 GSM2795094: CS14_B_3_5; Vitis vinifera; RNA-Seq SRP118973 SRS2544075 GSM2795094 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795094 GSM2795094 GEO Accession GSM2795094 SRX3219394 GSM2795095 GSM2795095: CS14_C_1_5; Vitis vinifera; RNA-Seq SRP118973 SRS2544076 GSM2795095 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795095 GSM2795095 GEO Accession GSM2795095 SRX3219395 GSM2795096 GSM2795096: CS14_C_2_5; Vitis vinifera; RNA-Seq SRP118973 SRS2544077 GSM2795096 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795096 GSM2795096 GEO Accession GSM2795096 SRX3219396 GSM2795097 GSM2795097: CS14_C_3_5; Vitis vinifera; RNA-Seq SRP118973 SRS2544078 GSM2795097 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795097 GSM2795097 GEO Accession GSM2795097 SRX3219397 GSM2795098 GSM2795098: CS14_B_1_6; Vitis vinifera; RNA-Seq SRP118973 SRS2544079 GSM2795098 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795098 GSM2795098 GEO Accession GSM2795098 SRX3219398 GSM2795099 GSM2795099: CS14_B_2_6; Vitis vinifera; RNA-Seq SRP118973 SRS2544080 GSM2795099 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795099 GSM2795099 GEO Accession GSM2795099 SRX3219399 GSM2795100 GSM2795100: CS14_B_3_6; Vitis vinifera; RNA-Seq SRP118973 SRS2544081 GSM2795100 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795100 GSM2795100 GEO Accession GSM2795100 SRX3219400 GSM2795101 GSM2795101: CS14_C_1_6; Vitis vinifera; RNA-Seq SRP118973 SRS2544082 GSM2795101 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795101 GSM2795101 GEO Accession GSM2795101 SRX3219401 GSM2795102 GSM2795102: CS14_C_2_6; Vitis vinifera; RNA-Seq SRP118973 SRS2544083 GSM2795102 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795102 GSM2795102 GEO Accession GSM2795102 SRX3219402 GSM2795103 GSM2795103: CS14_C_3_6; Vitis vinifera; RNA-Seq SRP118973 SRS2544084 GSM2795103 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795103 GSM2795103 GEO Accession GSM2795103 SRX3219403 GSM2795104 GSM2795104: CS14_B_1_7; Vitis vinifera; RNA-Seq SRP118973 SRS2544085 GSM2795104 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795104 GSM2795104 GEO Accession GSM2795104 SRX3219404 GSM2795105 GSM2795105: CS14_B_2_7; Vitis vinifera; RNA-Seq SRP118973 SRS2544086 GSM2795105 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795105 GSM2795105 GEO Accession GSM2795105 SRX3219405 GSM2795106 GSM2795106: CS14_B_3_7; Vitis vinifera; RNA-Seq SRP118973 SRS2544087 GSM2795106 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795106 GSM2795106 GEO Accession GSM2795106 SRX3219406 GSM2795107 GSM2795107: CS14_C_1_7; Vitis vinifera; RNA-Seq SRP118973 SRS2544088 GSM2795107 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795107 GSM2795107 GEO Accession GSM2795107 SRX3219407 GSM2795108 GSM2795108: CS14_C_2_7; Vitis vinifera; RNA-Seq SRP118973 SRS2544089 GSM2795108 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795108 GSM2795108 GEO Accession GSM2795108 SRX3219408 GSM2795109 GSM2795109: CS14_C_3_7; Vitis vinifera; RNA-Seq SRP118973 SRS2544090 GSM2795109 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795109 GSM2795109 GEO Accession GSM2795109 SRX3219409 GSM2795110 GSM2795110: CS14_B_1_8; Vitis vinifera; RNA-Seq SRP118973 SRS2544092 GSM2795110 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795110 GSM2795110 GEO Accession GSM2795110 SRX3219410 GSM2795111 GSM2795111: CS14_B_2_8; Vitis vinifera; RNA-Seq SRP118973 SRS2544093 GSM2795111 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795111 GSM2795111 GEO Accession GSM2795111 SRX3219411 GSM2795112 GSM2795112: CS14_B_3_8; Vitis vinifera; RNA-Seq SRP118973 SRS2544091 GSM2795112 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795112 GSM2795112 GEO Accession GSM2795112 SRX3219412 GSM2795113 GSM2795113: CS14_C_1_8; Vitis vinifera; RNA-Seq SRP118973 SRS2544094 GSM2795113 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795113 GSM2795113 GEO Accession GSM2795113 SRX3219413 GSM2795114 GSM2795114: CS14_C_2_8; Vitis vinifera; RNA-Seq SRP118973 SRS2544095 GSM2795114 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795114 GSM2795114 GEO Accession GSM2795114 SRX3219414 GSM2795115 GSM2795115: CS14_C_3_8; Vitis vinifera; RNA-Seq SRP118973 SRS2544096 GSM2795115 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795115 GSM2795115 GEO Accession GSM2795115 SRX3219415 GSM2795116 GSM2795116: CS14_B_1_9; Vitis vinifera; RNA-Seq SRP118973 SRS2544097 GSM2795116 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795116 GSM2795116 GEO Accession GSM2795116 SRX3219416 GSM2795117 GSM2795117: CS14_B_2_9; Vitis vinifera; RNA-Seq SRP118973 SRS2544098 GSM2795117 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795117 GSM2795117 GEO Accession GSM2795117 SRX3219417 GSM2795118 GSM2795118: CS14_B_3_9; Vitis vinifera; RNA-Seq SRP118973 SRS2544099 GSM2795118 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795118 GSM2795118 GEO Accession GSM2795118 SRX3219418 GSM2795119 GSM2795119: CS14_C_1_9; Vitis vinifera; RNA-Seq SRP118973 SRS2544101 GSM2795119 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795119 GSM2795119 GEO Accession GSM2795119 SRX3219419 GSM2795120 GSM2795120: CS14_C_2_9; Vitis vinifera; RNA-Seq SRP118973 SRS2544100 GSM2795120 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795120 GSM2795120 GEO Accession GSM2795120 SRX3219420 GSM2795121 GSM2795121: CS14_C_3_9; Vitis vinifera; RNA-Seq SRP118973 SRS2544103 GSM2795121 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795121 GSM2795121 GEO Accession GSM2795121 SRX3219421 GSM2795122 GSM2795122: CS14_B_1_10; Vitis vinifera; RNA-Seq SRP118973 SRS2544102 GSM2795122 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795122 GSM2795122 GEO Accession GSM2795122 SRX3219422 GSM2795123 GSM2795123: CS14_B_2_10; Vitis vinifera; RNA-Seq SRP118973 SRS2544104 GSM2795123 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795123 GSM2795123 GEO Accession GSM2795123 SRX3219423 GSM2795124 GSM2795124: CS14_B_3_10; Vitis vinifera; RNA-Seq SRP118973 SRS2544105 GSM2795124 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795124 GSM2795124 GEO Accession GSM2795124 SRX3219424 GSM2795125 GSM2795125: CS14_C_1_10; Vitis vinifera; RNA-Seq SRP118973 SRS2544106 GSM2795125 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795125 GSM2795125 GEO Accession GSM2795125 SRX3219425 GSM2795126 GSM2795126: CS14_C_2_10; Vitis vinifera; RNA-Seq SRP118973 SRS2544107 GSM2795126 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795126 GSM2795126 GEO Accession GSM2795126 SRX3219426 GSM2795127 GSM2795127: CS14_C_3_10; Vitis vinifera; RNA-Seq SRP118973 SRS2544109 GSM2795127 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795127 GSM2795127 GEO Accession GSM2795127 SRX3219427 GSM2795128 GSM2795128: CS14_B_1_11; Vitis vinifera; RNA-Seq SRP118973 SRS2544108 GSM2795128 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795128 GSM2795128 GEO Accession GSM2795128 SRX3219428 GSM2795129 GSM2795129: CS14_B_2_11; Vitis vinifera; RNA-Seq SRP118973 SRS2544110 GSM2795129 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795129 GSM2795129 GEO Accession GSM2795129 SRX3219429 GSM2795130 GSM2795130: CS14_B_3_11; Vitis vinifera; RNA-Seq SRP118973 SRS2544111 GSM2795130 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795130 GSM2795130 GEO Accession GSM2795130 SRX3219430 GSM2795131 GSM2795131: CS14_C_1_11; Vitis vinifera; RNA-Seq SRP118973 SRS2544113 GSM2795131 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795131 GSM2795131 GEO Accession GSM2795131 SRX3219431 GSM2795132 GSM2795132: CS14_C_2_11; Vitis vinifera; RNA-Seq SRP118973 SRS2544115 GSM2795132 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795132 GSM2795132 GEO Accession GSM2795132 SRX3219432 GSM2795133 GSM2795133: CS14_C_3_11; Vitis vinifera; RNA-Seq SRP118973 SRS2544112 GSM2795133 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795133 GSM2795133 GEO Accession GSM2795133 SRX3219433 GSM2795134 GSM2795134: CS14_B_1_12; Vitis vinifera; RNA-Seq SRP118973 SRS2544114 GSM2795134 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795134 GSM2795134 GEO Accession GSM2795134 SRX3219434 GSM2795135 GSM2795135: CS14_B_2_12; Vitis vinifera; RNA-Seq SRP118973 SRS2544116 GSM2795135 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795135 GSM2795135 GEO Accession GSM2795135 SRX3219435 GSM2795136 GSM2795136: CS14_B_3_12; Vitis vinifera; RNA-Seq SRP118973 SRS2544117 GSM2795136 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795136 GSM2795136 GEO Accession GSM2795136 SRX3219436 GSM2795137 GSM2795137: CS14_C_1_12; Vitis vinifera; RNA-Seq SRP118973 SRS2544118 GSM2795137 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795137 GSM2795137 GEO Accession GSM2795137 SRX3219437 GSM2795138 GSM2795138: CS14_C_2_12; Vitis vinifera; RNA-Seq SRP118973 SRS2544119 GSM2795138 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795138 GSM2795138 GEO Accession GSM2795138 SRX3219438 GSM2795139 GSM2795139: CS14_C_3_12; Vitis vinifera; RNA-Seq SRP118973 SRS2544120 GSM2795139 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using the Spectrum Plant Total RNA kit (Sigma-Aldrich) following the manufacturer’s instructions with some modifications (Fasoli et al., 2012). RNA quality and quantity were determined using a Nanodrop 2000 spectrophotometer (Thermo Scientific) and a Bioanalyzer Chip RNA 7500 series II (Agilent). 206 non-directional cDNA libraries were prepared from 2.5 μg of total RNA using the Illumina TruSeq RNA Sample preparation protocol (Illumina Inc., San Diego, CA, USA). Library quality was determined using the Agilent High Sensitivity DNA kit on the Agilent 2100 bioanalyzer, and the quantity was determined by quantitative PCR using the KAPA Library Quantification kit (KapaBiosystems). Illumina HiSeq 1000 gds 302795139 GSM2795139 GEO Accession GSM2795139