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Walls interspersed among these modules pivot out to create flexible exhibition spaces.
Figure 1 shows the architecture and interactions among these modules.
In this figure, the rectangular boxes specify the tool's modules and the dotted arrows indicate the dependencies among these modules.
The dynamic interplay among these modules controls the switch between the pluripotent/self-renewal state and the differentiated state by regulating gene expression at the level of chromatin state, transcription, post-transcription, and post-translation.
We then ask whether there are a few "conserved" modules among these modules.
Among these modules, two cohesins seem to be truncated.
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Among these module 3 genes was a NAC transcription factor encoded by Pavir.J16651.
Twenty-two genes are shared among all 4 of these modules and they are enriched for KEGG pathway oxidative phosphorylation and the GO category mitochondrial inner membrane.
Among these top modules, we found highly differentially expressed candidate genes and relevant cancer interactions in modules 143, 79 and 82.
Among these predicted modules, Teg152 and Teg154 are predicted to encode for type I antitoxins in S. aureus N315 strain (Table S1).
Among these ten modules, nine are statistically enriched (P < 0.05, Fisher's exact test, except for other processes).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com