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Participants were instructed to respond only to the colored events, and to use the mouse to indicate if the number was odd (press the left button) or even (press the right button); no responses were made to the non-probes in either task.
Baseline levels were normalized using the 500 ms interval prior to the non-probe stimulus.
Baseline levels of PD were normalized using the 500 ms interval prior to the non-probe stimulus.
Non-probe stimuli were presented for 1000 ms followed by a fixation cross which varied in duration from 900 2300 milliseconds (mean duration 1500 ms).
Probes were then floored to a value of 20 to avoid superficially high ratios in respect to non expressed probes.
F = number of non significant probes in the array.
For completeness, the complete datasets (including also the non overlapping probes) were also analyzed in parallel.
After high – stringency washing of non – hybridized probes, the macroarrays were digitally evaluated.
Non-specific binding was determined from fluorescence values of all non-specific probes.
While the number of cross-hybridization loci per probe ranged from 2 to 1615, the majority of non-specific probes cross-hybridized to between two and five locations (52.4% of type I non-specific probes and 65.2% of type II non-specific probes).
We studied how to select a minimum set of non-unique probes to identify the presence of at most d targets in a sample where each non-unique probe can hybridize to a set of targets.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com