We then removed at random one of the two paralogs and its rat (orangutan) ortholog and found the pair with the lowest d s among the remaining paralogs and the same set of six homologs was created.
We removed lenses at different stages starting at prim 22 (35 hpf), high pec (42 hpf) or long pec (48 hpf) and protruding mouth (72 hpf).
To trim PPM matrices, we removed columns at each flank until two consecutive columns with information content greater than 0.25 were encountered.
We removed edges at random, by which k was stepwise decreased, and recalculated L and C at each step, i.e. for each sampled network.
We removed links at a rate that keeps the average connectivity constant.
There was no difference in our overall effect estimates when we removed studies at increased risk of bias (appendix 8).
We evaluated cross type performance under field conditions using a seed burial study where we removed packets at three time periods to assess (i) fall germination, (ii) early spring germination and overwinter mortality, and (iii) peak germination and dormancy.
In an attempt to clarify this rather complex in vivo effect of HIF2α on neuroblastoma growth, we removed tumours at days 19 (just before the growth acceleration of HIF2α nodules) and 28 for controls and HIF2α(1 485) cells and at days 19, 28 and 35 for HIF2α nodules.
The time-course gene expression data was measured at 0, 0.55, 0.75 0.75, 1, 2, 4, 5, 5.5, 7, 8, 12, 18, 30, 48, and 72 [h] (16 time points) after stimulation of corticosteroid, but we removed data at 48 and 72 [h] (steady state profiles) for computational efficiency.
Motivated by the technique used in [16], where the authors considered the minimizers of nonquadratic functional, we removed the hinder at last.
Once we had placed all crickets in position, we removed the lids at the same end as the crickets' heads and left the room.
