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First-degree relationships discrepant with registry (13 samples) identified using PLINK were not initially excluded.
While test expansion and chamber aspect ratio were a key trait in both samples (identified using the loadings onto the robust principal components), filled (a shape variable, see Methods for full details) was a much stronger predictor in the upper Eocene than earlier in the sequence (Table 2).
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The location and identity of all samples is stored using a sample inventory software package, Pro-Curo (Brady Laboratories), and samples are identified using a bar coded label.
For NV GII, 134 samples were identified using GII-F1/R1/F2, SRII-1/2/3, and NKII-F/R/R2 to detect 31, 19, and 53 samples, respectively.
Functional groups of DOM samples were identified using FT-IR spectrophotometer (IRPrestige-21, Shimadzu, Japan).
Both samples were identified using operationalised computer algorithm criteria of DSM-IV major depressive disorder episode (MDD) irrespective of the current clinical diagnosis of the patients.
The platelet population in these whole blood samples was identified using flow cytometry.
Gene clusters representing similar expression profiles between uninjured epicardial and muscle control samples were identified using unsupervised, SOM clustering (Radius 7.0) with a maximum of 4500000 iterations.
Transcripts exhibiting differential expression between samples were identified using the NOIseq program in R [ 106].
Differentially expressed probes between shRNA and control samples were identified using the limma package (Smyth, 2005).
Differentially transcribed genes across samples were identified using the program SAM (Significance Analysis of Microarrays) version 4.0 [ 63].
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