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This difference between likelihoods was manifested in almost all cases with young clades, that is, with an RCA of 0.5 and 1.
The V/m ratio starts out around 0.4 for RCA = 0.5 but quickly approaches the equilibrium value of 1 at an RCA of 3. Hence, clades which are three times as old or older than the binding site half-life are expected to approach an equilibrium value of V/m = 1.
This clade has an estimated age of 43 Mio years and thus the BOE estimate of half-life time is likely to be less than 10 Mio years, that is, this clade would have an RCA of 4 or higher, based on the simulation results with four taxa.
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No. 9 is an RCA 77DX ribbon microphone, one of those iconic capsule-shaped mikes similar to the ones that Larry King and David Letterman keep on their desks.
This technique is comprised of two steps: rolling-circle amplification (RCA) of a short DNA multimer (e.g., a dimer for alphoid DNA) into 2-15 kb DNA branched molecules (that are poorly clonable in bacterial vectors) and subsequent assembly of the amplified molecules into long arrays by transformation- associated recombination (TAR) in yeast [ 24].
Microsoft is doing a root cause analysis (RCA) of the disruption, including steps to help prevent any future reoccurrence.
Polyaptamer DNA and graphene oxide (PA-GO) hybrid hydrogels were constructed by single-step rolling-circle amplification (RCA) of a DNA template in the presence of GO nanosheets.
Microscopy glass slides (Fisher Scientific, Premium microscope slides 12-544-4) were cleaned by using an RCA-1 solution of NH4OH/H2O2/H2O in the ratio 1 1 5 at 80 °C for 20 min. The cleaned glass slide was placed on the spin-coater (model P6700, Specialty Coating Systems Inc).
A limited literature describes RF for H but a detailed root cause analysis (RCA) of individual HE has not been published.
Rolling Circle Amplification (RCA) of DNA is a sensitive and cost effective method for the rapid identification of pathogenic fungi without the need for sequencing.
Rolling circle amplification (RCA) of DNA is a sensitive and cost effective method for the rapid identification of pathogens without the need for sequencing.
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