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Remarkably, many of these same categories were enriched in the mouse dataset, showing conservation of function between the two species among trans ceQTLs, particularly ion related categories.
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Consistent with previous studies [ 9– 12], the updated mouse KO dataset shows no statistical difference of P E between singletons and duplicates (44.8% versus 46.3%; P = 0.56).
The same general trend for the true positives is observed for the mouse-rat dataset shown in Figure 5 (maximum of 12996 when α is 0.52).
Dataset showing percentages of pairwise shared phamilies.
Although H3K4me2 is informative in human datasets, it was not informative in mouse dataset (result not shown).
Of all datasets examined, the laptop dataset showed the best classification accuracy (98.86%).
Therefore, the dataset shows no singularity issue.
This graph, using the PIOMAS daily ice volume dataset shows the rapid, and accelerating loss of ice.
We further show in the mouse dataset that dCaP captures genomic regions showing significant signal variations for TAL1 occupancy between two mouse erythroid cell lines.
Similarly, correlations of non-muscle human tissue in dataset H3 to mouse dataset M are lower and do not show a significantly higher correlation to any mouse muscle group – with one exception in the ST3 sample profile characterization where among non-muscle human tissue, brain and spinal cord had significantly higher correlation with mouse soleus than with non-soleus muscle profiles.
More broadly, 823 putative BRA targets exclusively found in the human ChIP-seq datasets show misregulation in mouse mutant embryos (Fig. 7C), underscoring the value of our new data.
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CEO of Professional Science Editing for Scientists @ prosciediting.com