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SRX5060466: RNA-Seq of Hermertia illucens L: late pupa stage
1 ILLUMINA (Illumina HiSeq 2000) run: 31.8M spots, 9.5G bases, 3.4Gb downloads

Design: After the total RNA extraction and DNase I treatment, magnetic beads with Oligo (dT) are used to isolate mRNA(for eukaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then cDNA is synthesized using the mRNA fragments as templates. Short fragments are purified and resolved with EB buffer for end reparation and single nucleotide A (adenine) addition. After that, the short fragments are connected with adapters. The suitable fragments are selected for the PCR amplification as templates. During the QC steps, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used in quantification and qualification of the sample library. At last, the library could be sequenced using Illumina HiSeqXTen.
Submitted by: Huazhong Agricultural University
Study: Transcriptome sequencing of black soldier fly
show Abstracthide Abstract
investigate the fat accumulation mechanism by transcriptome sequencing.
Sample: collected in late pupa stage
SAMN10465380 • SRS4076407 • All experiments • All runs
Library:
Name: L-pupa_2
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Runs: 1 run, 31.8M spots, 9.5G bases, 3.4Gb
Run# of Spots# of BasesSizePublished
SRR824228531,753,3489.5G3.4Gb2020-11-01

ID:
6829874

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