Exact(3)
However, we were not interested in analyzing size variations, as size variations can be compensated for by using a different size implant.
We present an automated microscopy-based, fast, high-throughput method for analyzing size and number of intracellular bacterial colonies in infected tissue culture cells.
We grouped the putative ceRNA pairs based on the #miRPBS with identical criteria as used in analyzing size of miRNA programs, resulting in 4 groups of 10,829,459, 12,443,877, 12,296,702, and 11,881,385 putative ceRNA pairs.
Similar(57)
We also examined the demographic consequences of variation in larval SAH by analyzing size-dependent mortality of larvae and juveniles in two separate ways.
In a first step, we analyze size effects.
For the plant we analyzed size at first reproduction and number of foliar nectaries.
In order to control some sources of variation related to sex, we analyzed size standardized adult individuals of both sexes.
The InDel polymorphisms were genotyped using a simple procedure that analyzed size polymorphisms of PCR products.
The Fl-FFF analyzed size-fractionated chemical compositions in colloidal materials trapped on the 1 kDa membrane.
We analyzed size-class distributions (SCDs) of species and plant functional types, and compared the performance of juvenile and adult age-classes.
We thus analyzed size-matched, rather than stage- or age-matched larvae that might be slower due to delayed development and smaller size.
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