If there is sufficient evidence (defined with the same quality metrics as above) to determine that the given individual does not have an alternative allele at the tested location, this information is stored in the database as a "SARA" (Same As Reference Assembly) position, which can be thought of as a computational genotyping assay.
One is the weight system, which on one hand distinguishes between conflicting evidence and absent evidence against adjacencies with the same level of support, and on the other hand detects a certain number of poorly supported adjacencies whose contexts in the three genomes suggest that they nevertheless merit inclusion in a solution.
Rather than the centerpiece of prosecution, witness testimony should be viewed more like trace evidence, scientists say, with the same fragility and vulnerability to contamination.
A qualitative decision of clinical relevance was established based on necessitated change in patient management, signs of local site infection or evidence of bacteraemia with the same organism.
Both lines of evidence are consistent with the same division and the variation that we observed in phylogenetic structure affects the behavior that we observe in the social stage.
However, despite evidence for association with the same two SNPs in two studies, we cannot be confident in these findings due the different directional effects of the SNP alleles.
Serologic evidence of infection with the same strain was found in 4 of 7 household members and in 3 of 46 nonhousehold contacts, with only 1 of the seropositive patients having a history of an ILI within the preceding year, which demonstrated unrecognized human infection with SIV.
Of note, ExonFinder also identifies novel exons/ASVs with EST evidence from the same species; users can choose whether or not to remain this information.
These findings provide suggestive evidence that activity in PCC and thalamus is sensitive to both LV and DV, though in distinct ways, together with weaker evidence that the same considerations apply to activity in VP and vmPFC/OFC.
DCM models with inputs to dorsal frontal regions had greater evidence than the same models with inputs to ventral frontal regions (e.g., families D and E better than A, B, and C; see Fig. 4 b ).
