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A three-dimensional phase field model of β → α transformation in polycrystalline Ti 6Al 4V (wt.%) alloys is formulated and used to study variant selection and microstructure evolution under different processing conditions and starting β phase textures.
In a French study, variant of the GGGA polymorphism from the ESR1 was associated with an increased risk of developing prostate cancer [28], [29].
In this study, variant sequences comprising 2.8% of the pooled DNA were detected, although sample pools of more than 18 genotypes were not examined.
In our previous study, variant genotypes of COX-2 rs20417 G>C (GC/CC) were associated with increased breast cancer risk.
All the statistical testing performed in this study—variant allele fraction comparison across different categories of somatic mutations, number of recurrent mutations, and dN/dS ratio suggest that mtDNA somatic substitutions accumulate largely neutrally.
In this study variant calls exceeding 20% of the total coverage value were compared to STS consensus haplotypes with the following considerations: (i) Length heteroplasmy (LHP) in C tracts was represented by the dominant variant (major molecule) in STS data [24].
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We study variants of the α-synchronizer by Awerbuch (1985) within a distributed message passing system with probabilistic message loss.
In this paper we study variants of d-is in which a feasible solution is a multiset of points that may satisfy only a subset of the stabbing requirements.
In the present study, variants of CD44 increased in patients with recurrent ampullary adenocarcinoma (Fig. 4).
Taken together, we concluded that in our study, variants in DMBT1 3′UTR region unlikely contribute to DASE.
Once a candidate gene had been selected for study, variants within the gene must be tested for association with phenotype.
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