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A probe set of 885 genes with standard deviations greater than 0.5 across 66 arrays was selected for further analyses.
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Based on these criteria 341 arrays were selected corresponding to 22 experimental batches encompassing 85 different treatments (Table 2).
Three differently shaped 300 μm long microneedle arrays were selected and fluorescein was applied either before or after piercing.
Optimum AGZO NSs enclosing highest density of nanorod (NR) arrays were selected to fabricate a hydrogen gas (H2) sensor.
Comparison between different designs, the layout of electrodes was optimized and an interdigital, pectinate, rectangular microelectrode arrays were selected as the main components of the cell-electrofusion chip.
The arrays were selected to include probe sets for several previously published prostate aggressiveness models [12] [16].
Genes that showed at least a 1.7 fold change from the time zero point in at least two arrays were selected for further analysis.
The samples for the tissue arrays were selected based on detailed evaluation of the autopsy reports followed by clinical and histological confirmation.
In the time course data, genes that showed at least a 1.7 fold change from the time zero point, in at least two arrays were selected for further analysis.
Zinc finger arrays were selected using the OPEN method essentially as previously described [26] but with a small number of alterations that improve the speed and throughput of the protocol.
Some of the genes on the TaqMan arrays were selected to validate our previous microarray studies and have been published earlier [12], while others were selected based on published clinical associations (e.g. colon cancer associated genes) or as normalization controls.
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CEO of Professional Science Editing for Scientists @ prosciediting.com