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For each B cell sample, we quantified the frequency of IgH sequences expressing a given isotype and examined the relationship between the isotype profiles to the mutation status.
Using a large cross sectional English sample, we quantified the association between weight status in children aged 4 5 and 10 11 year, characteristics of the food environment, and area deprivation.
For each tumor sample, we quantified expression levels of both tenascins and classified them into the following 4 categories with respect to their tenascin expression: absent, low, moderate and high, as described in Materials and Methods.
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In order to allow a comparison of parasite loads between the different BMA samples, we quantified the number of nucleated human cells using housekeeping gene (Albumin).
In the same set of breast cancer samples, we quantified the level of MYC mRNA.
In urine samples, we quantified creatinine, phosphate, and calcium by colorimetric assay (Cobas Amplicor; Roche Diagnostics, Indianapolis, IN, USA).
By comparing relative protein abundances in GA149-GFP and GFP samples we quantified 450 proteins, 20 of which were strongly enriched in poly-GA aggregates (Fig. 4a, Table 1).
Using a novel grid-based landscape-wide sampling approach, we quantified pollinator communities within ten 1 km × 1 km landscapes representing independent gradients in OSR and SNH availability.
To ensure that the relative abundance of EBV miRNAs was not sample-dependent, we quantified the expression levels of these 25 BART miRNAs in 12 additional NPC tissues and c666-1 cells and analyzed the correlation of EBV miRNA expression pattern among these samples.
For HBoV-positive samples, we then quantified viral loads by real-time PCR (Technical Appendix).
To validate these data derived from pooled samples, we also quantified Cyp1a1 expression in SootH-instilled mice on the single-animal level (n = 4).
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