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Data-reuse provides tremendous opportunity to extract new knowledge from existing experiments, and offers a unique opportunity for robust, multi-'omics analyses by merging metadata (information about experimental design, biological samples, protocols) and data from multiple experiments.
Data from multiple experiments are summarized in Table 1.
When data from multiple experiments were combined, statistical analysis was performed using the two-tailed unpaired t-test.
The quantitative data from multiple experiments demonstrate that the Myo Va motor domain (41-505) significantlyicantly more binding activity compared to the 800-881 construct (Fig. 2D, p<0.015).
Data from multiple experiments are summarized in Fig. 3. Splenocytes and bone marrow cells from mice infected 3 days prior with DENV-2 had the highest frequencies of hCD45+ antigen-positive cells using the 3H5 mAb with lower frequencies of hCD45+ antigen-positive cells detected in mice studied 5 or 7 days post infection (Fig. 3A and B).
Data from multiple experiments were pooled for final analysis.
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Images used for all figures were highly representative of data collected from multiple experiments.
The retrieved data are from multiple experiments and are displayed in a bar chart and tables for download.
oaCGH data obtained from separate strains using the same chip design performs consistently enough to allow for the integration and direct comparison of the data generated from multiple experiments.
Reviewer #1: This manuscript by Hunt et al. is based on the analyses of several different types of data collected from multiple experiments that have been described in previous papers.
Our previous 3D structure was derived using data obtained from multiple experiments, including photoaffinity cross-linking, chemical modification interference, complementary modification, cryo-AFM, mutagenesis, ribonuclease probing, primer extension, 41) and oligo targeting.
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