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Using standard gating approaches (i.e., doublet exclusion, live cell gating, cell-specific marker gate, see Supplementary Fig. 7), the population of live, single cells (72 77% of total) was identified and analyzed across experimental conditions (PDL, MaxGel and bECM) and time points (15 DIV and 30 DIV) (Fig. 6a).
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Twenty-three sines in total were identified to be tissue-specific.
However, seven outlier AONs (6% of the total) were identified.
Similarly, four outlier AONs (6% of the total) were identified, i.e., H30A, H58A, H64A and H34A2.
Notably, most SNPs (141 in total) were identified within CDSs involved in drug resistance (MDR/DR).
Twenty-five serins in total were identified that evaluated focal therapy in the primary setting (Table 1) [15–39].
A total of 28 weakly expressed chromosomal regions, spanning 408 Mb in total, were identified in CD34+ cells.
Approximately 5,000 20,000 transfrags per tissue, or 11 45% of the total, were identified as potentially novel splice forms.
alpina genes (7.78% of the total) were identified as essential for growth using the FBA method (Additional file 3).
The importance of both ionic and electronic contributions to the total conductivity was identified.
A total of 37 RCTs was identified.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com