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Discussion groups allow partisans to swap analysis and opinion, not always typing in a native language.
Table 2 The results of our Size, Weight and Power (SWaP) analysis along with a complete list of subsystems and their control circuits.
In this analysis, we performed intriplicate analysis of global gene expression, including dye swap analysis, for 2 pairs of sibling Sirt1−/− and Sirt1+/− mice.
In the swap analysis, the MCC for validation set was dropped to 0.377.
Note that, in the swap analysis, the MCC for validation set was only 0.377.
Two independent experiments were performed to each array using two different biological samples and dye swap analysis.
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The concordant copy number changes detected in dye-swap analysis were considered to be true changes.
The four replicates (two intra-array and two deriving from the dye-swap analysis) were t-tested using the SAM software and considering the lowest False Discovery Rate.
However, the CNV region on chromosome 32 was validated in dye-swap analysis, which suggests that the 76 Kb-sized CNV region on chromosome 32 might be real.
In this study we compare the roles of protein structure and ubiquitylation in regulating Ngn2 and NeuroD stability and activity by undertaking a domain-swap analysis between the two proteins.
In addition to the dye-swap analysis, we also performed whole-genome SNP genotyping for the genomes of the donor and cloned dogs using an Illumina CanineHD 170 K SNP array to obtain a more reliable interpretation of the de novo CNVs.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com