Accession | CRX503403 |
Organism | Eospalax fontanierii baileyi |
Title | BSA_1 |
BioProject | PRJCA010603 |
BioSample | SAMC874547 |
Platform | Illumina NovaSeq 6000 |
Library |
Library name |
Construction protocol |
Strategy |
Source |
Selection |
Layout |
|
Total RNA was used as input material for the RNA sample preparations. Briefly, mRNA was purified from total RNA by using poly-T oligo-attached magnetic beads. Fragmentation was carried out using divalent cations under elevated temperature in First Strand Synthesis Reaction Buffer(5X). First strand cDNA was synthesized using random hexamer primer and M-MuLV Reverse Transcriptase, then use RNaseH to degrade the RNA.Second strand cDNA synthesis was subsequently performed using DNA Polymerase I and dNTP. |
RNA-Seq |
TRANSCRIPTOMIC |
PCR |
PAIRED
|
|
Processing |
Planned read length (bp) for mate 1: 150
Planned read length (bp) for mate 2: 150
|
Release date | 2022-09-08 |
Run |
Run accession |
Run data file information |
File name | File size (MB) |
CRR567497 |
CRR567497_f1.fq.gz
CRR567497_r2.fq.gz
|
1,500.01
1,552.85
|
|
Submitter | Baohui Yao (735310030@qq.com) |
Organization | Gansu Agricultural University |
Date submitted | 2022-09-08 |