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However the limit of detection (LOD) of using pre-amplified vs. non-amplified cDNA samples, and its impact on the technical performance of the PCR array have not been fully characterized.
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This behavior can be explained by Raman scattering of InAs QD array having not only different size but also different QD aspect ratio (QD height/base size).
Although the aforementioned work considers the near-field processing of the spherical microphone array, near-field or mixed field source localization via a spherical microphone array has not yet been studied.
Chromosomal and plasmid genes present on the array had not been distinguished from each other in the original construction phase.
To our knowledge, this GC array has not been previously reported, even among reports of other gram-negative isolates.
To date, the extent of cross hybridisation using the Affymetrix whole transcript Human Gene 1.0 ST array has not been assessed.
Study on the transcriptional response to the Gram-positive bacterium SS2 by using the Affymetrix GeneChip Porcine Genome Array has not been reported until now.
Despite its availability and support, the Tag4 array has not been widely adopted (examples that have used it include Ericson et al. 2010; North and Vulpe 2010; Zakrzewska et al. 2011), and it will likely be subsumed by next generation DNA sequencing (NGS) methods (Smith et al. 2012).
In the literature, photoconductivity, pH sensitivity, noise, and channel length effects in the same set of NW FET arrays have not been studied in detail.
These arrays have not previously been used for this type of study.
While first attempts to describe the performance of HuEx in comparison to conventional arrays have been made [2], systematic studies of signal behavior on HuEx arrays have not been described, and comparative analysis of this behavior with 3' targeted arrays like the U133Plus2 series is unknown.
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