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To assess the role of mRGCs in negative masking, we measured the wheel running activity of mice subjected to a short photocycle of 4 h light and 4 h dark over several days (Figure 6).
Before masking, we provide results only for selected matrix families that we discuss in the text.
For repeat masking, we used a combination of the Repbase Dipteran library [ 29] and the B. tryoni-specific repeats identified above.
After masking, we provide results for any matrix family that appeared statistically significant in all three tests before applying the Bonferroni correction for multiple testing.
To identify probes for removal (masking) we used BLAST to compare the Affymetrix target sequences from this array to identify homologous regions in release 2.0 of the D. yakuba genome.
After masking, we obtained transcript abundances for 7024 that were dispersed relatively evenly across the entire genome and generally tracked gene density: X: 1118, 2L: 1236, 2R: 1421, 3L: 1408, 3R: 1811, 4: 30.
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The masks we wear, right?
We risk replacing the face with the mask we have created.
We clear flooded masks; we take off our BCDs (buoyancy control devices, where the air lives).
You think we are not so different, in our different cities, behind the masks we wear underneath our masks.
When he takes off his mask, we see that it is General Yen.
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