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"Appropriate data sets (including microarray data, protein or DNA sequences, atomic coordinates or electron microscopy maps for macromolecular structures, and climate data) must be deposited in an approved database, and an accession number or a specific access address must be included in the published paper.
Therefore, before publication, large data sets (including microarray data, protein or DNA sequences, atomic coordinates or electron microscopy maps for macromolecular structures, and climate data) must be deposited in an approved database and an accession number or a specific access address must be included in the published paper.
Therefore, before publication, large data sets (including microarray data, protein or DNA sequences, and atomic coordinates or electron microscopy maps for macromolecular structures) must be deposited in an approved database and an accession number provided for inclusion in the published paper.
Neumann's ideal experiment involves collecting gene microarray data, protein levels, metabolite levels, clinical phenotypes, and serum biomarkers in one experiment.
In this study, we are interested in identifying statements declaring the deposition of biological data (such as microarray data, protein structure, gene sequences) in public repositories.
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The transcriptional networks based on microarray data, protein-protein interaction networks based on high-throughput yeast two-hybrid type of experiments and metabolic networks based on reaction annotation of the individual proteins coded by the genome are some examples.
Several studies have proposed integrated analyses of microarray data and protein-protein interaction (PPI) networks to find diagnostic subnetwork markers.
The combination of microarray data, proteomics data, protein-protein interaction data, and other -omics data, in another word, studying the interrelationship of all the components that comprise a system is a trend in identifying genes involved in the aging process.
This section reports the results of an extensive simulation study, which were conducted on both synthetic and publicly available microarray data and protein abundance mass spectrometry data.
We first analyzed the human microarray data for protein trafficking-related genes that were up-regulated in colon carcinoma Caco2 cells upon differentiation.
Consistent with the microarray data, Cdk2 protein levels were significantly elevated in mutant primary cultures (normalized fold change 2.2 ± 0.06).
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