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Application of Deviation metric for threshold height analysis allows the correct localization of peaks and valleys in the map and determining "defective" areas on a wafer.
Quantitation of cyclin D1 intensity was performed by using ImagePro by generating a DAPI-based nuclear map and determining the relative cyclin D1 intensity per nucleus, which was subsequently separated into four bins based on relative intensity.
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For instance, suppose that Jones has looked at a map and determined how to drive from New York City to Chicago though he has not done so: just get on Interstate 80 and go west.
2) Coverage of Maps/Gap Analysis We can look at the results from individual cells to better assess the timely coverage of the map and determine where gaps in coverage exist.
Establishing a suitable mapping population is the first step in constructing a map and determines its quality.
We present Bismark, a software package to map and determine the methylation state of BS-Seq reads.
Mean values from three independent cell preparations were used to establish the map and determine relationships between the luminal subsets by unsupervised hierarchical clustering.
We vertically arranged walnut cdBES based on their order within BAC contigs and the order of BAC contigs along the genetic map and determined homology of each cdBES with the grape, v.145, poplar, v.210, apple, v.196, Medicago truncatula, v.198, cucumber, v.122, and strawberry, v.226 non-redundant protein databases (http://phytozome.jgi.doe.gov/) using BLASTX and P < 1 E-5.
In this study, applying a recently developed method for estimating tissue deformation dynamics from spatially and temporally limited dye-marking data to chick limb development, we generated a precise tissue deformation map and determined the spatio-temporal patterns of deformation characteristics; the accuracy of estimated quantities was statistically guaranteed through cross-validation.
Then if differences in gene expression are the major contributor of phenotypic variation, one can identify, map, and determine the contributions of thousands of genes, many of which have small effects, in two steps (ASE SNP identification followed by association analyses) that explain the majority of genetic variation effects for a trait.
Say you are by the museum, go on the map and determine your exact location.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com