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As an important component of PolSAR image interpretation, target decomposition[2] expresses the average mechanism as the sum of independent elements in order to associate a physical mechanism with each pixel, which allows the identification and separation of scattering mechanisms for purposes of classification[3, 4].
Our characterization of established pancreatic tumour cell lines with the respect to the genetic alterations in this potential cancer target family finally provides suitable cell systems for data interpretation, target validation, as well as preclinical models for the development of novel targeted cancer drugs.
Thus, although WES has some limitations in terms of data analysis, management, and interpretation, target capture enables the study of a more restricted and personalized target genomic region, thereby simplifying data analysis and reducing experimental time and costs.
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Proposed topographic analysis enables ((GC times GC)) forensic interpretation across target petroleum biomarkers, while including the nuances of lesser-known non-target biomarkers clustered around the target peaks.
The primary aim of this work is to provide quantitative peak-level interpretation beyond target biomarkers, with the end goal of robust differentiation between petroleum sources that share regional commonalities, and therefore, have highly correlated (GCtimes GC) fingerprints.
The fifth link, named "extrapolation," connects the theoretical score interpretation and target score interpretation.
We harness the rich compound diversity across the (GCtimes GC) biomarker (hopanes and steranes) topography to provide potentially transformative compound-cognizant interpretation beyond target compound analysis.
We exploit this compound diversity across the ((GC times GC)) topography to provide quantitative compound-cognizant interpretation beyond target compound analysis with petroleum forensics as a practical application.
As a result, the use of GAPDH as a single, unverified reference gene would invariably lead to erroneous interpretation of target gene regulation.
Next, the possibility that using scaling factors of NFRPL19/29, NFACTB or NFGAPDH may substantially alter the interpretation of target gene expression regulation in NGF induced neuronal differentiation was investigated.
AFM results are, therefore, consistent with the interpretation that target hybridization leads to the formation of distinct motifs at pH 6 and 8, which are, respectively, a triplex and a duplex.
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