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R2 value is shown for each cell.
The R2 value is shown in for each cell.
For each cell line the 1% threshold is determined independently.
Repli-Seq was performed in duplicate for each cell line.
The R2 value is shown for each cell.
Water fluxes were measured every 5 min for each cell.
First, they created a reference value for each cell.
A region of interest was defined for each cell and the average fluorescent intensity was calculated.
For each cell, the DAPI channel was used to outline the nucleus area.
Transfection efficiency and conditions were optimized for each cell line used.
Each distance matrix was calculated using the union of DEGs for each cell type.
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CEO of Professional Science Editing for Scientists @ prosciediting.com