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One way to overcome the limitation of the LPCD model, and to obtain better results from a perceptual point of view, is to require that the sample order, in the 1D case, is preserved (thus introducing memory in the system).
In addition, we randomly permuted the sample order in the miRNA (or mRNA) profiles and repeated the analysis.
The average lead-time required for a sample order in the last year, out of average lead-time during the past three years decreased about 80%.
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In the Co Pt system, a cooling experiment can drive a sample ordered in the cubic L12 structure inside the two-phase region involving L12 and the tetragonal L10 structure.
Technicians were unaware of the origin of each sample, and the order in which samples were tested was randomized.
Females were added to the Stage 2 sample in order to increase power in the analysis.
Scaled quantities of carrier RNA added to the samples were capped at 5 μg per sample in order to minimize interference in downstream steps.
First, we used a rather small convenient sample in order to perform more in depth interviews that allow for multi-level analysis.
The photocurrent measurements are carried out in a metallic sample holder in order to avoid noises.
PCR — polymerase chain technology — allows analysis of DNA in a blood or urine sample in order to identify a disease.
Limit activity in the room where you taking the sample, in order to avoid stirring up asbestos fibers.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com