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Comparing the contact patterns measured by sensors with the synthetic matrices, we found an (R_{0}) ratio significantly different from 1 for all the households (see Table 3) and systematically larger than 1, indicating that a random mixing assumption may not be adequate to describe contact patterns within households.
When examining translation in non-contractile vs. contractile collagen matrices, we found more than 3-fold unique, named genes differing at the level of ribosome recruitment in IPF myofibroblasts compared to control myofibroblasts (1753 vs. 575).
Within a particular cluster (e.g. genes related to extracellular matrices), we found that multiple genes were differentially regulated during diapause.
Concerning matrices, we found statistically significant inverse associations with BPD, HC, and BW when using maternal serum, and for AC and EFW with cord serum.
Using 125 TFBS position weight matrices, we found six transcriptional factors potentially involved in the regulation of the 69 out of 331 non-mitochondrial DAP3 coexpressed genes.
Concerning matrices, we found more robust associations with head-related outcomes when using maternal serum, while the associations with the rest of the outcomes were clearer with cord serum.
Similar(51)
If we compare the Match results (dot at the left upper corner) with those by our original matrix (blue line), new mono-nucleotide (red line) and di-nucleotide (magenta) matrices, we find that the randomized OFr for Match is much higher comparing to the other PWMs for the sensitivity around 60%.
When GNL terms were included in the total stiffness matrix, we found that load-path bifurcation preceded tissue failure regardless of the form of the damage model.
First, using transition probability matrix, we found evidence of (unconditional) state dependence in all types of innovation, with product innovators having the strongest persistent behavior.
For this matrix, we found inverses for one matrix, nine submatrices, and nine submatrices.
From the gene matrix, we found that some O-glycosylation required enzymes are detectable, such as OGT, POFUT1/2, XYLT1, POMT2, etc.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com