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Recruitment and baseline data will be used to develop statistical models that relate the independent variables to the dependents: Multimorbidity patterns of similar severity will be identified by methods of supervised learning (methods of recursive partitioning like CART [Classification and Regression Trees], logistic regression).
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Moreover, more than 10% of the candidate genes could be identified by both methods, most of which were clustered on chromosome 1 (bin1.07).
With species going extinct faster than they can be identified by traditional methods, a group of taxonomists has been developing DNA barcoding to speed up their work.
Heterozygous individuals can be identified by different methods such as examination of progeny e.g. by clinical examination or necropsy, analysis of enzyme activity in blood, and genotyping of animals by genomic analysis.
This may necessitate that outliers be identified by statistical methods [ 57– 58], rather than preconceptions of the likely range of values.
Besides the above contiguously conserved regions that can be identified by available methods, there are a large number of conserved regions with Interspersed Conserved Segments (ICS) that cannot be identified by the above methods.
Such authorities can be identified by computational methods alone through examining the patterns of connections among the nodes; this is how many internet search engines identify authoritative web pages.
The use of different normalization methods or measures of variance is expected to influence the outcome of a search by RefGenes, but overall it is unlikely that genes that exhibit a high stability within a RT-qPCR experiment would not be identified by either of these methods at the microarray level.
Any PSG cDNA sequences that could still not be identified by this method were determined by BLAST analysis of the mouse genome database using known fragments of the sequence to be determined.
Nutritional epidemiological studies will be identified by a range of methods including computer-aided literature searches of medical databases [MEDLINE, EMBASE, BIOSIS, CINAHL, CAB Abstracts (for Human Nutrition), Scopus, Dietary Assessment Calibration/Validation Register, and LILACS].
In summary, necrotic cell death in vitro or in vivo cannot be determined using a single method and preferably should be identified by a combination of different methods.
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