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SRX9694812: GSM4978003: StAgo1-GFP H2O 1; Solanum tuberosum; miRNA-Seq
1 ION_TORRENT (Ion Torrent Proton) run: 12M spots, 229.6M bases, 183.4Mb downloads

Submitted by: NCBI (GEO)
Study: Convolutional neural network modelling: advancing identification of true mRNA cleavage sites
show Abstracthide Abstract
Degradome sequencing is commonly used to generate high-throughput information on mRNA cleavages by small RNAs. Here we developed an extension module based on a deep learning convolutional neural network (CNN) in a machine learning environment to discriminate false from true cleavage sites applied on datasets from potato (Solanum tuberosum, St) and the oomycete pathogen Phytophthora infestans (Pi). The core of the CNN module is a stochastic gradient descent optimizer with cyclical learning rate (CLR) which together with Bayesian optimization scored a validation accuracy of 100%. To verify the recognition of cleavage sites we applied the module on Arabidopsis thaliana microRNA cleavages. Our module managed to recognize all cleavages, confirming the reliability of the module. When applying this new model to evaluate our data, 7.3% of all cleavage windows represented true cleavages distributed as 214 sites in P. infestans and 444 sites in potato. The sRNA landscape of the potato-P. infestans interaction is complex with uneven sRNA production and cleavage regions. In total, 222 endogenous Pi-sRNAs, 565 endogenous St-sRNAs, 91 trans-acting Pi-sRNAs and 14 trans-acting St-sRNAs were discovered from our datasets. Groups of self-regulatory sRNAs, and sRNAs generated from effector sequences like RXLR and Crinklers suggest dual effector functions. In the potato genome, resistance genes were most targeted mainly as self-regulation but also as results of a trans-action event. Our new analytic model is freely accessible for anyone working on complex biological systems. Overall design: 9 small RNA samples sequenced from Co-IP. 3 replicates for each of the following: StAgo1-GFP H2O, StAgo1-GFP 11388, StAgo1-GFP 88069. 4 small RNA libraries were sequenced. 2 replicates from each of the following: Potato leaves (cv. Sarpo Mira) inoculated with H20 or 88069. 10 degradome libraries were sequenced. 2 replicates from each of the following: Mycelia of P. infestans strains 88069 or PiAgo1-GFP. Leaf samples of Potato (cv. Bintje) inoculated with H2O. Infected leaf samples with P. infestans strains 88069 or PiAgo1-GFP.
Sample: StAgo1-GFP H2O 1
SAMN17098845 • SRS7891421 • All experiments • All runs
Library:
Instrument: Ion Torrent Proton
Strategy: miRNA-Seq
Source: TRANSCRIPTOMIC
Selection: size fractionation
Layout: SINGLE
Construction protocol: Inoculated leaves were harvested and flash frozen in liquid nitrogen. StAGO1a-GFP and control Pi-GFP immunoprecipitations were performed with anti-GFP antibody (Chromotek, gtm-100). Barcoded sequencing libraries were constructed using the Ion Total RNA-Seq Kit v2 and Ion Xpress barcode primers. Sequencing was performed on the Ion Proton platform using the Ion PI™ Hi-Q™ Sequencing 200 Kit (Thermo Fisher Scientific).
Experiment attributes:
GEO Accession: GSM4978003
Links:
Runs: 1 run, 12M spots, 229.6M bases, 183.4Mb
Run# of Spots# of BasesSizePublished
SRR1326443411,993,869229.6M183.4Mb2021-05-05

ID:
12680618

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