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Experiment information
Accession CRX534724
Organism Olea europaea subsp. europaea
Title Leccino_12h_2
BioProject PRJCA012898
BioSample SAMC974921
Platform Illumina NovaSeq 5000
Library
Library name Construction protocol Strategy Source Selection Layout
The mRNA was enriched by binding to the ployA tail of the mRNA by A-T complementary pairing using magnetic beads with Oligo (dT). Then fragmentation buffer was added to break the mRNA into short fragments. The mRNA was used as a template to synthesize the first strand cDNA with random hexamers, and then buffer, dNTPs and DNA polymerase I were added to synthesize the second strand cDNA. Double-stranded cDNA was subsequently purified using AMPure XP beads. The purified double-stranded cDNA was then subjected to end repair, A-tail addition and sequencing adapter ligation, followed by fragment size selection with AMPure XP beads, and finally PCR enrichment to obtain the final cDNA library. RNA-Seq TRANSCRIPTOMIC PolyA PAIRED
Processing Planned read length (bp) for mate 1: 150
Planned read length (bp) for mate 2: 150
Release date2024-11-01
Run
Run accession Run data file information
File nameFile size (MB)
CRR599853 CRR599853_f1.fq.gz
CRR599853_r2.fq.gz
1,206.42
1,272.33
SubmitterTianyi Wang (wangty02@163.com)
OrganizationChinese Academy of Forestry
Date submitted2022-11-04