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SRX15694082: GSM6239632: sample.ginkgo.11588701; Escherichia coli str. K-12 substr. MG1655; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 5M spots, 1.5G bases, 576.3Mb downloads

Submitted by: NCBI (GEO)
Study: Transcriptional Response to Inducers for E. coli and B. subtilis
show Abstracthide Abstract
Sequencing technologies, in particular RNASeq, have become critical tools in the design, build, test, learn cycle for synthetic biology. They provide a better understanding of synthetic designs and they help identify ways to improve and select designs. While this data is beneficial to design, its collection and analysis is a complex, multi-step process that has implications both on discovery and reproducibility of experiments. Additionally, tool parameters, experimental metadata, and normalization of data and standardization of file formats present challenges that are computationally intensive. This calls for high-throughput pipelines expressly designed to handle the combinatorial and longitudinal nature of synthetic biology. In this paper, we present a pipeline to maximize analytical reproducibility of RNASeq for synthetic biologists. We also explore the impact of reproducibility on the validation of machine learning models. Overall design: 1,344 samples were collected in quadruplicate, and there are non-induced controls for each organism.
Sample: sample.ginkgo.11588701
SAMN29018093 • SRS13390484 • All experiments • All runs
Library:
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA was extracted using Magjet RNA extraction kit (Thermo) according to manufacturer's instructions. RNA quality was assessed using Tapestation (Agilent). KAPA RNA Hyperprep kit (Roche) was used for ribosomal RNA depletion and Illumina compatible library preparation.
Experiment attributes:
GEO Accession: GSM6239632
Links:
Runs: 1 run, 5M spots, 1.5G bases, 576.3Mb
Run# of Spots# of BasesSizePublished
SRR196434445,012,1591.5G576.3Mb2022-06-28

ID:
22321873

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