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Using our I2D database [81], [82] we examined known human protein-protein interactions for a binomial distribution to define such hubs, and failed to find such a distribution, hence we are unable to further study any such relationship.
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Frequency distribution was compared to binomial distribution to evidence the phase separation and atom clustering.
We have devoted two lines in Table 9 to the binomial distribution to illustrate its inaccuracy.
It uses a negative binomial distribution to model total variation.
We used normal approximation of binomial distribution to construct confidence intervals (CI) for each indicator.
Finally, we used a negative binomial distribution to estimate the statistical significance of the peaks.
Thus, we developed a model that uses a negative-binomial distribution to approximate an overdispersed Poisson distribution.
The probability mass function for the binomial distribution is defined to be B k ; n, p = n k p k 1 − p n − k, where n k = n ! k ! n − k !, n is the number of trials, k is the number of successes, and p is the probability of success.
The probability mass function of binomial distribution is defined in the following way: (18).
Comparisons are made with the generalized negative binomial distribution (GNBD) defined by Jain and Consul ([1971]) and the exponentiated-exponential geometric distribution (EEGD) defined by Alzaatreh et al. ([2012b]).
The KBIN procedure follows from basic probability concepts, to control the probability that the number of false positives V is not larger than k to be α, that is, where V is the number of false positives, assumed to follow a Binomial distribution, with k defined by the user.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com