Settings in FastFinder are displayed with this symbol (cogwheel):
All settings are saved in your browser (not user login specific, but browser specific)
Table settings
You can define which columns you want to display. Greyed-out columns cannot be hidden.
Drag and drop the columns via to specify your desired order.
Table settings in Analyses - Details tab contain an additional 'sort wells' by column or row selection.
Graph settings
Amplification or Melt curves
- The curve color can be organized either by dye, by result or by target (only applicable for amplification graphs).
- The chart type can be set to baseline corrected or amplification (or melt curve or melt peaks, respectively for melt assays):
- Baseline corrected: visualization of the amplification data following processing by the algorithm.
- Amplification: visualization of the raw amplification data.
- Choose between logarithmic or linear scale for your amplification graphs.
- Enable or disable the option to show only your selected data (other data is removed from the background) or all data.
- Enable showing Cq/Tm values for the selected data.
- Permanently show control or reference curve data when selecting a sample.
- Fill in your preferred X- and Y- axis min/max values.
Press "Save" to save your changes or "Reset scales" to go back to the default settings.
Endpoint analyses
- Select the chart type of your preference: normalized or raw data.
- You can toggle the button to only show your selected data and/or to show control data when selecting a sample.
Plate settings
- Select under Target type how you want to visualize the result: by the overall assay result or by a single target result. For endpoint analyses, select by target fluorescence to display a heatmap.
- Enable the Highlight replicates for selected wells to highlight all wells that belong to the same replicate group as the selected well. The wells that don't belong to the same replicate group will be faded out.
Press "Save" to save your changes.