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A prototypic ARC that implements all specification standards accordingly
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Genome sequencing of blackcurrant (Ribes nigrum)
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HHU Plant Biochemistry / CEPLAS RNASeq Workshop 2022
Creative Commons Attribution Non Commercial Share Alike 4.0 InternationalUpdated -
This ARC presents diverse data from MibiNet members to illustrate the application of MibiNet-specific SWATE templates and showcase examples of metadata annotation.
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Dominik Brilhaus / Facultative CAM in Talinum
Creative Commons Attribution 4.0 InternationalReversible Burst of Transcriptional Changes during Induction of Crassulacean Acid Metabolism in Talinum triangulare.
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Felix Jung / deepSTABp
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Algae cultures were grown mixotrophically (TAP). After 24h of 35°C/40°C the cells were shifted back to room temperature for 48h. 'omics samples were taken.
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Usadellab / Quinoa_Chileanfieldtrial
Creative Commons Attribution 4.0 International"QUINOA DIVERSITY- Quinoa Phenotypic and Genotypic Diversity for Yield and Composition"
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Quantification of cell growth is central to any study of photoautotrophic microorganisms. However, cellular self-shading and limited CO2 control in conventional photobioreactors lead to heterogeneous conditions that obscure distinct correlations between the environment and cellular physiology. Here we present a microfluidic cultivation platform that enables precise analysis of cyanobacterial growth with spatio-temporal resolution. Since cyanobacteria are cultivated in monolayers, cellular self-shading does not occur, allowing homogeneous illumination and precise knowledge of the photon-flux density at single-cell resolution. A single chip contains multiple channels, each connected to several hundred growth chambers. In combination with an externally applied light gradient, this setup enables high-throughput multi-parameter analysis in short time. In addition, the multilayered microfluidic design allows continuous perfusion of defined gas mixtures. Transversal CO2 diffusion across the intermediate polydimethylsiloxane membrane results in homogeneous CO2 supply, with a unique exchange-surface to cultivation-volume ratio. Three cyanobacterial model strains were examined under various, static and dynamic environmental conditions. Phase-contrast and chlorophyll fluorescence images were recorded by automated time-lapse microscopy. Deep-learning trained cell segmentation was used to efficiently analyse large image stacks, thereby generating statistically reliable data. Cell division was highly synchronized, and growth was robust under continuous illumination but stopped rapidly upon initiating dark phases. CO2-Limitation, often a limiting factor in photobioreactors, was only observed when the device was operated under reduced CO2 between 50 and 0 ppm. Here we provide comprehensive and precise data on cyanobacterial growth at single-cell resolution, accessible for further growth studies and modeling.
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CEPLAS / Germann-2023
Creative Commons Attribution 4.0 InternationalA systematic overexpression approach reveals native targets to increase squalene production in Synechocystis sp. PCC 6803
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HHU Institute of Plant Genetics / Lan_2025_Ppd-H1
Creative Commons Attribution Non Commercial No Derivatives 4.0 InternationalPPD-H1 Improves Stress Resistance and Energy Metabolism to Boost Spike Fertility under High Ambient Temperatures
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Natural-Variation-and-Evolution / Microscopy_Collection / map-by-seq_CLSM-stacks
Creative Commons Attribution 4.0 InternationalUpdated -
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Oxa was applied to human cells and checked for antifibrotic effects
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HHU Plant Biochemistry / Wrobel-2023-CastorBeanEndospermProteome
Creative Commons Attribution 4.0 InternationalMapping the castor bean endosperm proteome revealed a metabolic interaction between plastid, mitochondria, and peroxisomes to optimize seedling growth
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HHU Plant Biochemistry / Talinum fruticosum genome
Creative Commons Attribution 4.0 InternationalUpdated