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RFM mutagenesis will provide a useful complementary approach for scanning proteins to quickly identify those regions carrying fundamentally important information for protein folding, stability or activity.
Array comparative genomic hybridization (aCGH) is an efficient approach for scanning entire genomes to seek variations in genomic copy number variations, genotyping and medical genetics.
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The QCL approach offers higher speeds for scanning large tissue arrays, but the nature of the DF-IR system is such that much smaller times become accessible for certain types of measurements.
In order to reduce the limitations of the previous LD-based approaches, we developed a method for scanning genome-wide SNP genotype data for population-specific selective sweeps that have reached fixation, in which homozygosity for haplotypes in two populations are compared.
We present an approach for fabricating customized, replaceable tips for scanning probe microscopy of critical dimension and high aspect ratio structures.
Here, we devise and apply a regularisation approach specifically tailored for scanned images.
DNA sequence polymorphism allows a more precise analysis of selective effects but the approach of scanning genomes for regions of low nucleotide diversity [ 17, 31] is rarely simultaneously conducted with FST scans.
The approach of scanning genomes for FST outliers is becoming a standard in molecular ecology [ 42] and the number of studies that inferred candidate loci for adaptation through this approach is increasing rapidly [ 43- 45].
The results of this research imply how the accurate contact point detection aided by the new sensor yields a reliable approach for surface scanning and stability measure calculation.
There have been two principal approaches to scanning the genome for disease genes, which are culminating in photo-finish results by the proponents of each method.
Another approach involves scanning the genome for sequences that show signs of having been under selection (see Wright and Gaut 2005; Nielsen et al. 2005).
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