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Microarray results identified a number of genes that were differentially expressed between NP or IVD cells and AC cells.
The microarray results identified various miRNAs that were differentially regulated in the exosome of MHFMD and ESHFMD samples relative to healthy controls, and a scatter plot was generated.
Microarray results identified 26 miRNAs, of which 14 miRNAs, which were not previously reported in HCC, showed >20-fold difference in expression between patients with HCC and healthy volunteers.
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Our microarray analysis results identified one of the genes upregulated by Tax as CDKN1A, which codes p21CIP1/WAF1, known as Cdk inhibitor 1.
After validating the microarray results, we identified miR-183 as a potential PC oncogenic miR.
Similar to microarray results, we identified an increase in SNORA12 methylation in response to infection exclusively within the Healthy group.
After qRT-PCR validation of microarray results, we identified 154 differentially expressed genes of which 104 changes their expression in response to UV treatment, suggesting differential regulation in these two cell lines.
A final example demonstrates the ability of the system to translate results identified by microarray technologies, or other related high throughput technologies, to identify likely Xenopus homologues.
In total, three replicate microarray hybridizations were performed and analysis of the results identified 271 differentially expressed ESTs (> 1.5 fold).
Gene network analysis of complex datasets, such as DNA microarray results, aims to identify relevant structures that help the understanding of a certain phenotype or condition.
Microarray results of three replicates identified a total of 553 probes corresponding to 495 genes that were significantly differentially expressed ≥2-fold between untreated and caffeine-treated HT29 cells.
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