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Application of a variant of identity (2.1).
application of a variant of the proposed approach, where a SVM-based classifier is used instead of the developed BN.
Our approach is based on an application of a variant generalized weak linking strongly indefinite problem developed by Schechter and Zou [21]; also see Chen and Ma [22].
(10) Our approach is based on an application of a variant and generalized weak linking theorem for strongly indefinite problem developed by Schechter and Zou [16], also see Chen and Ma [11].
(i) Construction of a family of bounded Cauchy Fantappié-type integrals C ϵ (ii) Estimates for C ϵ − C ϵ ∗ (iii) Application of a variant of identity (2.1) Step (i).
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Application of a GSEA variant [51], the Levene test for homogeneity of variance as modified by Brown and Forsythe (LBF), [52] identified several pathways that included both positive and negative regulators of cholesterol homeostasis.
This paper proposes the application of a modified variant, called MQEPS, of the quantum-inspired evolutionary algorithm based on P systems (QEPS) to the time frequency atom decomposition for analyzing radar emitter signals.
Here we describe the application of a rare variant collapsing method to a large genome-wide SNP dataset, the Wellcome Trust Case Control Consortium rheumatoid arthritis (RA) GWAS.
The application of a rare variant analysis method (Li and Leal 2008; Morris and Zeggini 2010), which accumulates information from multiple rare SNP alleles within a genic region, identified an association between RA and the TNFAIP3 gene.
In a previous study we have shown that the expression of Ang-1, Ang-2, Tie-1 and Tie-2 mRNA is significantly higher in arthritic tissue of CIA mice, and that the application of a splice variant of TIE-1 ameliorates disease severity, reduces synovial vascularisation and bone destruction [ 33].
These observations were based on the application of a 10% minor variant (or "minor allele frequency", MAF) threshold for detection – the same threshold used in four other studies to establish the presence of heteroplasmy in only 25% of individuals tested.
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