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The CD133 and CD10 expressions were split into high- and low-level groups using recursive descent partition analysis, as described by Hoffmann et al. [39].
When GalNAc-T3 and β-catenin expressions were split into groups of either positive or negative, their immunoprofiles were 10.2 –/–, 33.1, +/−, 35.4 −/+, and 21.3% +/+.
When ZNF143/MIB-1 ZNF143/MIB-1wexpressionsnto groups of either strong/were or high/low, their immunoprofilesplite 53.6% weak/low (98 cases); 14.2% strong/low (26 cases); 18.0% weak/hinto(33 cases); and 14.2% strongroups (26 cases).
Similar(57)
MUC4-negative cells or cells with low MUC4 expression were split 24 h before treatment.
Gene expression is split into quartiles based on RPKM.
Variance of the difference in gene expression was split between subgroups of genes with homogeneous variance [ 72].
When GalNAc-Ts expression was split into groups of either positive (weak to strong staining) or negative, the GalNAc-T3/6 immunoprofile was 39.4 −/−, 36.2 +/− 6.3 −/+, and 18.1% +/+.
To inject the tautology, the initial expression is splitted into several pieces.
293T cell lysates or RRL expression reactions were split and purified in parallel using the F and O purification approaches.
In order to optimize the predictor power and avoid over-fitting expression values were split into a training set (2/3 of the data) and a test set (1/3 of data).
For gene expression analysis islets were split into groups of 60, cultured for 24 hours in a 5% CO2 atmosphere in RPMI 1640 supplemented with 100 U/ml penicillin, and 100 µg/ml streptomycin.
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