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The relative impact of the different family designs and allele frequencies at the mutation could not be differentiated with these simulations.
Unlike previous whole-transcriptome analyses in Anabaena, deep sequencing provides information on all transcripts and can help identify 5' and 3' ends and characterize operon structure; however, transcriptional start sites versus processing sites cannot be differentiated with these methods.
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A few species could not be differentiated with the three suggested enzymes and for these, other enzymes were selected.
These peaks could not be statistically differentiated, with the exception of extension rotation at head/C1 and posterior shear translation at C7/T1.
Neuronal and glial cells could be differentiated with this method and heterogeneity was distinguishable among cells when analyzed on the single cell level.
The Val66Met polymorphism was differentiated with the NlaIII restriction enzyme.
All genotypes were differentiated with the exception of the two C. aurantium accessions.
The set of differential equations is differentiated with respect to the boundary condition chosen and the resulting partial differential equations are solved by a finite-difference method.
These groups were strongly differentiated, with a microsatellite based ϕst of 0.23 (p < 0.01) (Table 1).
All of these three GAs were well differentiated with coexisting morphological spectrum of MDA.
To confirm these data, we used ASCs differentiated with ATRA for 8 days and co-transfected the cells with either anti-let-7e or a control antimiR.
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