Flow Cell Chart

The Flow Cell Chart displays color-coded quality metrics per tile for the entire flow cell, and has the following features:

You can select the displayed metric, cycle, and base through the dropdown lists.
The color bar to the right of the chart indicates the values that the colors represent.

The chart is displayed with tailored scaling by default, or can be fixed by checking the Fix Scale checkbox.

Tiles that have not been measured or are not monitored are gray.
By right-clicking an image you can copy it to the clipboard.

You can monitor the following quality metrics with this chart:

Intensity—This chart displays the intensity by color and cycle of the 90% percentile of the data for each tile.
FWHM—The average full width of clusters at half maximum (in pixels). For a more detailed description, see http://en.wikipedia.org/wiki/Full_width_at_half_maximum.
% Base—The percentage of clusters for which the selected base has been called.
%Q>20, %Q>30—The percentage of bases with a quality score of 20 or 30 or higher, respectively. These charts are generated after the 25th cycle, and the values represent the current cycle. A check box appears that lets you toggle between cumulative (include previous cycles) or not (just display current cycle).
Median Q-Score—The median Q-Score over all basesfor the current cycle. These charts are generated after the 25th cycle.
Density—The density of clusters for each tile (in thousands per mm2).
Density PF—The density of clusters passing filter for each tile (in thousands per mm2).
Clusters—The number of clusters for each tile (in millions).
Clusters PF—The number of clusters passing filter for each tile (in millions).
Error Rate—The calculated error rate, as determined by a spiked in PhiX control sample. If no PhiX control sample is run in the lane, this chart is not available.
% Phasing, % Prephasing—The percentage of molecules in a cluster for which sequencing falls behind (phasing) or jumps ahead (prephasing) the current cycle within a read.
% Aligned—The percentage of the sample that aligned to the PhiX genome.
% Perfect Reads—The percentage of reads that align perfectly, as determined by a spiked in PhiX control sample. If no PhiX control sample is run in the lane, this chart is not available.
Corrected Intensity—The intensity corrected for cross-talk between the color channels and phasing and prephasing.
Called Intensity—The intensity for the called base.
Signal to Noise—The signal to noise ratio is calculated as mean called intensity divided by standard deviation of non called intensities.

 

© 2011-2012 Illumina, Inc. All rights reserved.

Rev. August 20, 2012