Sentence examples for mutants is represented from inspiring English sources

A list of all common genes between all three mutants is represented in table S7.

The expression levels in the mutants are represented relative to that in wild type (assigned a value of 1).

Class 3 mutants are represented by three loci, each of which shows reduced VPC induction.

A myc tag was added to each of these SOCS3 mutants, and exogenous SOCS3 mutants were represented by the detection of myc tag.

In RCC10 cells, type 1 VHL mutants were represented by constructs coding for pVHL with a deletion of amino acid residues 114 to 178 (del 114 178), a double point mutant RC161/2QW, the L188Q mutation, as well as control cells infected with a retrovirus lacking any VHL sequence.

For j > 0, the probability of having j mutants in the patch in generation t is given by p j ≡ (A t i) j, where i is a vector representing the initial distribution of the mutant: a single mutant is represented as i ≡ (1,0,...,0 T, where T denotes transpose.

Ewens showed that 1 b / ∑ i = 1 n − 1 1 i is the probability that a mutant is represented b times in n samples and the estimate of θ should be (3) θ ^ = 1 l ∑ j = 1 l S j a ′ n j, where a ′ n j = ∑ i = 1 + z n j − 1 − z 1 i [ 9].

For example, the 104 bp phyB deletion (E124 mutant) was represented on our custom microarrays by three probes at the 'standard' staggering of 49 bp (Table  1, Figure  5A and Additional file 1: Figure S5), while the smaller 28 bp and 4 bp deletions in the hy1 (E99) and max2 (E207) mutants were each represented just once at the same 'standard' staggering, respectively.

On the basis of this calculation each mutant plasmid is represented approximately 160 times in the screen.

It is likely that mutant DNA is represented at a very low level in these samples and this might explain the different results that we obtained with these techniques.

Since our major concern is the study of the conditions for establishment and ultimate fixation of increased coherence, all scenarios are characterized by initial conditions for genotypic frequencies, in which the mutant A1 is represented at low frequency and frequencies at the B-locus are close to equilibrium.