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This enabled us to construct consolidated lists of platform-independent tissue-specific genes using a set of complementary measures.
This enabled us to construct a comprehensive functional association network of differentially expressed genes using a natural language processing algorithm.
The results were consistent in all these centrality measures; hub genes using a combined network were more representative than hub genes using a single data source network.
We classified the identified genes using a similar method previously described (Kang et al. 2016).
(A) Initial screening of miR-139-5p miR-139-5p miR-139-5pmicroarray assay, bioinformatargetredictions and the luciferase reporter assay.
Jennifer Doudna, co-inventor of CRISPR Cas9 technology, or the ability to program genes using a special enzyme, spoke about the promises of this technology onstage at SXSW this afternoon.
In this study, we demonstrate the important process of validating potential reference genes using a non-model species.
Fine-mapping of these loci along with sequence and expression analysis, is underway to clone the genes using a map-based cloning strategy.
We identified 3,750 miRNA candidate genes using a computational pipeline combining RNAfold and TripletSVM algorithms.
Then molecular signatures are developed based on these genes using a nearest-centroid prediction method [47].
In compiling the gene signature, t-tests returned a list of 33 genes using a ENFP <3.
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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