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SRX20625954: RNA-seq of B. subtilis: WT monoculture
1 ILLUMINA (Illumina NovaSeq 6000) run: 10.4M spots, 3.1G bases, 997.6Mb downloads

Design: First, the ribosomal RNAs from both eukaryotes and prokaryotes were depleted from total RNA samples. The remained RNAs were fragmented into around 250~300 bp and then reverse-transcribed into double-stranded cDNAs which subsequently went through end repair, A tailing and adapter ligation. After fragments size selection and PCR amplification, the metatranscriptome library was ready for library QC and sequencing. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Quantified libraries will be pooled and sequenced on Illumina platforms, according to effective library concentration and data amount required.
Submitted by: Technical university of Denmark
Study: Competition for iron shapes metabolic antagonism between Bacillus sub-tilis and Pseudomonas
show Abstracthide Abstract
Assessing the mechanism of antagonism between Bacillus subtilis NCIB 3610 and a Pseudomonas marginalis soil isolate
Sample: DK1042 monoculture
SAMN35564843 • SRS17925585 • All experiments • All runs
Library:
Name: B3
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Runs: 1 run, 10.4M spots, 3.1G bases, 997.6Mb
Run# of Spots# of BasesSizePublished
SRR2486186710,379,1613.1G997.6Mb2023-11-29

ID:
28054803

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