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The encapsulated array was filled with argon gas, serving as an ionization medium in the small cavities of the MPFDs.
The inclusion of the photonic crystal array provided a 33% enhancement of the PL intensity (i.e., enhancement of sample 4 over sample 3), and an additional improvement of 38% was observed when the photonic crystal array was filled with silver.
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The array is filled up with values (deltas) in the following manner: 1.
If k s is greater than one, then the array is filled, ignoring each k s −1 row and column, starting at the centre point y, x (see Fig. 1b).
If k s equals 1, then the centre of the block is shifted to the point y, x and all the values that fit into a frame with dimensions h × w are assigned (see Fig. 1a); If k s is greater than one, then the array is filled, ignoring each k s −1 row and column, starting at the centre point y, x (see Fig. 1b).
Empty features on the array were filled with randomly generated probes that had G+C content and length comparable to the C. albicans probes and that acted as controls for non-specific binding.
The remaining spots on each 44 K array were filled with probes from the X chromosome (11745) and all of the autosomes (12053).
This process is repeated until all the phototube arrays are filled for normal operation.
The remaining ~ 1 M positions on the screening arrays were filled with non-coding variants based on their distribution across the genome.
The array of 16 channels was filled with a replaceable sieving polymer, and a size-dependent, electrophoretic separation of the DNA fragments was performed in all channels in less than 10 min, representing a 30-fold increase in throughput compared to that on a single-capillary instrument.
The Department of Zoology had laid out a fine array of displays and the room was filled with groups of visitors chattering noisily to members of staff and research students.
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