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Exact(25)
The single cube trials were similar except that the other cubes in the array were not visible.
Non-unique probesets (i.e. interrogating different transcript variants from same genes) that represent <4% of the entire array were not masked out.
Only 1227 base pairs had read depths less than 3, and only 425 bases included on the array were not sequenced at least once.
As a result, the mean proportion of looking time for the virtually novel array were not significantly different from that expected from chance probability (t(23) = −0.624, p>.1).
Even for this group of regulated genes, transcriptional regulation seems doubtful because expression peaked at different times in the cell cycle for the different genes, and many flanking genes in the same polycistronic gene array were not regulated.
While coverage was not complete because repeat sequences were masked out of the array capture, only 425 bases included on the capture array were not sequenced, all of these were adjacent to masked repeat sequence and none were in exons.
Similar(35)
This array is not entirely random.
The first phase of improvements, replacing all the electronics and communications at the array, is not expected to cause any interruption in observations.
The array is not uniformly accessed during the code execution.
But traditional physical characteristic dots array is not fitted in high temperature forging measurement conditions.
A customized PD array was not available, so we used a single PD instead.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com