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In our primary search for platforms we identified numerous examples that sought to collect and share personal health data and information of different types.
To find comparable sets of measurements made on both platforms, we identified RT-PCR probes and microarray probe sets that queried not only the same gene, but also the same set of transcript isoforms as determined by Refseq accession numbers.
By combining the results from the two microarray platforms, we identified 150 differentially expressed genes that were bound by SMAD4 in their promoter regions upon activation by TGF-β (See Additional File 4 – Table S1).
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Based on our observations of industry practices and the roles of crowds in crowdfunding platforms, we identify several of the shortcomings of pure crowds, including their ineffectiveness in providing heavy-duty due diligence, distortion in the wisdom of the crowds due to herding, social influence, and home bias, and high management costs associated with a lack of a single voice.
Using a genome-wide and piggyBac transposon-based genetic screening platform, we identified the PVT1 gene as a regulator of Gemcitabine sensitivity and showed that functional inactivation of the PVT1 gene led to enhanced Gemcitabine sensitivity in human pancreatic cancer ASPC-1 cells.
Using iTRAQ MALDI-TOF MS/MS platform, we identified 904 proteins with high confidence scores as determined with SEQUEST [18], PeptideProphet [19] and ProteinProphet [20] computational tools.
Using the Ion Torrent platform, we identified 29 microsatellite loci, of which seven were polymorphic.
Using this platform, we identified a protein (SAA) known to be elevated in active SJIA.
RESULTS: While we were able to previously identify only 456 genes affected by ST with the Affymetrix platform, we identified 1927 individual genes with the AB platform.
30 33 From this consensus-driven platform, we identified the target disease, population and explored standardised measures that inform the observation for the required time period.
By sequencing transcripts using the SOLiDTM 3 Plus platform, we identified new targets expected to potentiate the survival and replication of the pathogen in adverse environments.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com