SRX2225778 Vlaspik 8dpp-1 SRP090949 PRJNA345040 Reads are from cucumber cv. 'Vlaspik' fruit peel at 8 days post pollination (dpp). The reads are from one biological replicate, comprised of equal amounts of pooled RNA from two cucumbers. RNA was extracted with the Trizol method, cleaned using RNeasy cleanup kit (Qiagen), DNase treated for 15 min. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library preparation kit. After QC and quantitation all 12 libraries were combined into one pool. This pool was loaded on two lanes of an Illumina HiSeq 2500 Rapid Run flow cell (v1) and sequenced in a 50bp single end format (SE50) using Illumina Rapid SBS reagents. Base calling was performed by Illumina Real Time Analysis (RTA) v1.18.61 and output of RTA was demultiplexed using Illumina Bcl2fastq v1.8.4. Two lane files were merged. SRS1732453 SAMN05856085 Vlaspik 8dpp-1 RNA-Seq TRANSCRIPTOMIC unspecified Illumina HiSeq 2500 SRX2225801 Vlaspik 8dpp-2 SRP090949 PRJNA345040 Reads are from cucumber cv. 'Vlaspik' fruit peel at 8 days post pollination (dpp). The reads are from one biological replicate, comprised of equal amounts of pooled RNA from two cucumbers. RNA was extracted with the Trizol method, cleaned using RNeasy cleanup kit (Qiagen), DNase treated for 15 min. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library preparation kit. After QC and quantitation all 12 libraries were combined into one pool. This pool was loaded on two lanes of an Illumina HiSeq 2500 Rapid Run flow cell (v1) and sequenced in a 50bp single end format (SE50) using Illumina Rapid SBS reagents. Base calling was performed by Illumina Real Time Analysis (RTA) v1.18.61 and output of RTA was demultiplexed using Illumina Bcl2fastq v1.8.4. Two lane files were merged. SRS1732454 SAMN05856086 Vlaspik 8dpp-2 RNA-Seq TRANSCRIPTOMIC unspecified Illumina HiSeq 2500 SRX2225834 Gy14 16dpp-2 SRP090949 PRJNA345040 Reads are from cucumber cv. 'Gy14' fruit peel at 16 days post pollination (dpp). The reads are from one biological replicate, comprised of equal amounts of pooled RNA from two cucumbers. RNA was extracted with the Trizol method, cleaned using RNeasy cleanup kit (Qiagen), DNase treated for 15 min. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library preparation kit. After QC and quantitation all 12 libraries were combined into one pool. This pool was loaded on two lanes of an Illumina HiSeq 2500 Rapid Run flow cell (v1) and sequenced in a 50bp single end format (SE50) using Illumina Rapid SBS reagents. Base calling was performed by Illumina Real Time Analysis (RTA) v1.18.61 and output of RTA was demultiplexed using Illumina Bcl2fastq v1.8.4. Two lane files were merged. SRS1732455 SAMN05856095 Gy14 16dpp-2 RNA-Seq TRANSCRIPTOMIC unspecified Illumina HiSeq 2500 SRX2225835 Gy14 16dpp-3 SRP090949 PRJNA345040 Reads are from cucumber cv. 'Gy14' fruit peel at 16 days post pollination (dpp). The reads are from one biological replicate, comprised of equal amounts of pooled RNA from two cucumbers. RNA was extracted with the Trizol method, cleaned using RNeasy cleanup kit (Qiagen), DNase treated for 15 min. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library preparation kit. After QC and quantitation all 12 libraries were combined into one pool. This pool was loaded on two lanes of an Illumina HiSeq 2500 Rapid Run flow cell (v1) and sequenced in a 50bp single end format (SE50) using Illumina Rapid SBS reagents. Base calling was performed by Illumina Real Time Analysis (RTA) v1.18.61 and output of RTA was demultiplexed using Illumina Bcl2fastq v1.8.4. Two lane files were merged. SRS1732456 SAMN05856096 Gy14 16dpp-3 RNA-Seq TRANSCRIPTOMIC unspecified Illumina HiSeq 2500 SRX2225836 Vlaspik 8dpp-3 SRP090949 PRJNA345040 Reads are from cucumber cv. 'Vlaspik' fruit peel at 8 days post pollination (dpp). The reads are from one biological replicate, comprised of equal amounts of pooled RNA from two cucumbers. RNA was extracted with the Trizol method, cleaned using RNeasy cleanup kit (Qiagen), DNase treated for 15 min. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library preparation kit. After QC and quantitation all 12 libraries were combined into one pool. This pool was loaded on two lanes of an Illumina HiSeq 2500 Rapid Run flow cell (v1) and sequenced in a 50bp single end format (SE50) using Illumina Rapid SBS reagents. Base calling was performed by Illumina Real Time Analysis (RTA) v1.18.61 and output of RTA was demultiplexed using Illumina Bcl2fastq v1.8.4. Two lane files were merged. SRS1732457 SAMN05856087 Vlaspik 8dpp-3 RNA-Seq TRANSCRIPTOMIC unspecified Illumina HiSeq 2500 SRX2225840 Vlaspik 16dpp-1 SRP090949 PRJNA345040 Reads are from cucumber cv. 'Vlaspik' fruit peel at 16 days post pollination (dpp). The reads are from one biological replicate, comprised of equal amounts of pooled RNA from two cucumbers. RNA was extracted with the Trizol method, cleaned using RNeasy cleanup kit (Qiagen), DNase treated for 15 min. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library preparation kit. After QC and quantitation all 12 libraries were combined into one pool. This pool was loaded on two lanes of an Illumina HiSeq 2500 Rapid Run flow cell (v1) and sequenced in a 50bp single end format (SE50) using Illumina Rapid SBS reagents. Base calling was performed by Illumina Real Time Analysis (RTA) v1.18.61 and output of RTA was demultiplexed using Illumina Bcl2fastq v1.8.4. Two lane files were merged. SRS1732458 SAMN05856088 Vlaspik 16dpp-1 RNA-Seq TRANSCRIPTOMIC unspecified Illumina HiSeq 2500 SRX2225856 Vlaspik 16dpp-2 SRP090949 PRJNA345040 Reads are from cucumber cv. 'Vlaspik' fruit peel at 16 days post pollination (dpp). The reads are from one biological replicate, comprised of equal amounts of pooled RNA from two cucumbers. RNA was extracted with the Trizol method, cleaned using RNeasy cleanup kit (Qiagen), DNase treated for 15 min. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library preparation kit. After QC and quantitation all 12 libraries were combined into one pool. This pool was loaded on two lanes of an Illumina HiSeq 2500 Rapid Run flow cell (v1) and sequenced in a 50bp single end format (SE50) using Illumina Rapid SBS reagents. Base calling was performed by Illumina Real Time Analysis (RTA) v1.18.61 and output of RTA was demultiplexed using Illumina Bcl2fastq v1.8.4. Two lane files were merged. SRS1732459 SAMN05856089 Vlaspik 16dpp-2 RNA-Seq TRANSCRIPTOMIC unspecified Illumina HiSeq 2500 SRX2225879 Vlaspik 16dpp-3 SRP090949 PRJNA345040 Reads are from cucumber cv. 'Vlaspik' fruit peel at 16 days post pollination (dpp). The reads are from one biological replicate, comprised of equal amounts of pooled RNA from two cucumbers. RNA was extracted with the Trizol method, cleaned using RNeasy cleanup kit (Qiagen), DNase treated for 15 min. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library preparation kit. After QC and quantitation all 12 libraries were combined into one pool. This pool was loaded on two lanes of an Illumina HiSeq 2500 Rapid Run flow cell (v1) and sequenced in a 50bp single end format (SE50) using Illumina Rapid SBS reagents. Base calling was performed by Illumina Real Time Analysis (RTA) v1.18.61 and output of RTA was demultiplexed using Illumina Bcl2fastq v1.8.4. Two lane files were merged. SRS1732460 SAMN05856090 Vlaspik 16dpp-3 RNA-Seq TRANSCRIPTOMIC unspecified Illumina HiSeq 2500 SRX2225899 Gy14 8dpp-1 SRP090949 PRJNA345040 Reads are from cucumber cv. 'Gy14' fruit peel at 8 days post pollination (dpp). The reads are from one biological replicate, comprised of equal amounts of pooled RNA from two cucumbers. RNA was extracted with the Trizol method, cleaned using RNeasy cleanup kit (Qiagen), DNase treated for 15 min. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library preparation kit. After QC and quantitation all 12 libraries were combined into one pool. This pool was loaded on two lanes of an Illumina HiSeq 2500 Rapid Run flow cell (v1) and sequenced in a 50bp single end format (SE50) using Illumina Rapid SBS reagents. Base calling was performed by Illumina Real Time Analysis (RTA) v1.18.61 and output of RTA was demultiplexed using Illumina Bcl2fastq v1.8.4. Two lane files were merged. SRS1732461 SAMN05856091 Gy14 8dpp-1 RNA-Seq TRANSCRIPTOMIC unspecified Illumina HiSeq 2500 SRX2225913 Gy14 8dpp-2 SRP090949 PRJNA345040 Reads are from cucumber cv. 'Gy14' fruit peel at 8 days post pollination (dpp). The reads are from one biological replicate, comprised of equal amounts of pooled RNA from two cucumbers. RNA was extracted with the Trizol method, cleaned using RNeasy cleanup kit (Qiagen), DNase treated for 15 min. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library preparation kit. After QC and quantitation all 12 libraries were combined into one pool. This pool was loaded on two lanes of an Illumina HiSeq 2500 Rapid Run flow cell (v1) and sequenced in a 50bp single end format (SE50) using Illumina Rapid SBS reagents. Base calling was performed by Illumina Real Time Analysis (RTA) v1.18.61 and output of RTA was demultiplexed using Illumina Bcl2fastq v1.8.4. Two lane files were merged. SRS1732462 SAMN05856092 Gy14 8dpp-2 RNA-Seq TRANSCRIPTOMIC unspecified Illumina HiSeq 2500 SRX2225934 Gy14 8dpp-3 SRP090949 PRJNA345040 Reads are from cucumber cv. 'Gy14' fruit peel at 8 days post pollination (dpp). The reads are from one biological replicate, comprised of equal amounts of pooled RNA from two cucumbers. RNA was extracted with the Trizol method, cleaned using RNeasy cleanup kit (Qiagen), DNase treated for 15 min. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library preparation kit. After QC and quantitation all 12 libraries were combined into one pool. This pool was loaded on two lanes of an Illumina HiSeq 2500 Rapid Run flow cell (v1) and sequenced in a 50bp single end format (SE50) using Illumina Rapid SBS reagents. Base calling was performed by Illumina Real Time Analysis (RTA) v1.18.61 and output of RTA was demultiplexed using Illumina Bcl2fastq v1.8.4. Two lane files were merged. SRS1732463 SAMN05856093 Gy14 8dpp-3 RNA-Seq TRANSCRIPTOMIC unspecified Illumina HiSeq 2500 SRX2225952 Gy14 16dpp-1 SRP090949 PRJNA345040 Reads are from cucumber cv. 'Gy14' fruit peel at 16 days post pollination (dpp). The reads are from one biological replicate, comprised of equal amounts of pooled RNA from two cucumbers. RNA was extracted with the Trizol method, cleaned using RNeasy cleanup kit (Qiagen), DNase treated for 15 min. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library preparation kit. After QC and quantitation all 12 libraries were combined into one pool. This pool was loaded on two lanes of an Illumina HiSeq 2500 Rapid Run flow cell (v1) and sequenced in a 50bp single end format (SE50) using Illumina Rapid SBS reagents. Base calling was performed by Illumina Real Time Analysis (RTA) v1.18.61 and output of RTA was demultiplexed using Illumina Bcl2fastq v1.8.4. Two lane files were merged. SRS1732464 SAMN05856094 Gy14 16dpp-1 RNA-Seq TRANSCRIPTOMIC unspecified Illumina HiSeq 2500