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An application example for the identification of environmentally assisted cracking mechanisms in petroleum refineries is presented.
A large-scale case study example for the identification of an industrial low-density polyethylene (LDPE) reactor model is presented.
In another example, for the identification of host regulators for HIV replication mentioned as above, overlaps were very limited among the three studies described (Table 1).
Another example for the identification of chemical sources is monitoring triphenyltin (TPT) in Lower Saxony (Germany): After finding high tributyltin (TBT and TPTT concentrations in sediments and biota from a marina, concentrations of both chemicals were measured in fish at around 100 stations in Lower Saxony (Germany) in 1996.
What this paper concludes is that there is too much variation within human genomes, and too much gene flow in modern populations, to make the simplistic classification of people into races useful for biomedicine, for example for the identification of differential risk to disease or pharmaco-sensitivity.
Besides the use of distinct measures, it could also be attractive to have one general measure of functioning that incorporates several distinct measures, but provides one summary score to quantify overall level of functioning, for example for the identification of older adults at risk of poor functional outcome.
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Within the MCDA model for example, the "identification of the risk-benefit criteria; assessment of the performance of each option against the criteria; the assignment of weight to each criterion; and the calculation of the weighted scores at each level and the calculation of the overall weighted scores"[ 13] would constitute risk evaluation.
We then explicate the dual relationship between sparse functional identification and decoding and provide examples for the identification of low-rank temporal DSP kernels of complex cells.
An example workflow for the identification of cis-regulatory TFBSs linked to a disease is outlined in the following section, and is illustrated in Figure 2. Given a set of high-throughput sequencing data from an individual, the short sequences are individually aligned to a reference human genome sequence.
The approaches we describe are robust for some conclusions; for example, the identification of genomic regions that are missing or highly diverged from the query sequence, and regions, such as the proteorhodopsin gene locus, where genes and gene order vary in conserved patterns.
By integrating genome-wide copy number profiling data and gene expression data, lists of genes associated with response to specific therapies can be enriched for biologically relevant targets (for example, the identification of FGFR1 amplification as a modulator of tamoxifen response [ 13]).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com