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1 hurdle regression models using the negative binomial distribution.
2 generalized linear model based on a negative binomial distribution.
3 tructed for each sub-counties based on a log-binomial distribution.
4 and models the cell abundances using a beta-binomial distribution.
5 ell doublets are modeled by employing a Beta-binomial distribution.
6 The 95% CIs were approximated using a binomial distribution.
7 of DGE tools that are based on the negative binomial distribution.
8 th more closely than the often-used negative binomial distribution.
9 epsilona values obeyed laws of binomial distribution.
10 ribution, and in paired data based on a beta-binomial distribution.
11 ting the secondary case data with a negative binomial distribution.
12 termined by using an exact method based on a binomial distribution.
13 ng generalized linear models with a negative binomial distribution.
14 t size, due to the properties of the Poisson-binomial distribution.
15 -Seq reads were assumed to follow a negative binomial distribution.
16 hedral species, which do not follow a simple binomial distribution.
17 given reference position are sampled from a binomial distribution.
18 ds is generally slower than predicted by the binomial distribution.
19 image quality ranks were calculated from the binomial distribution.
20 ly modelled as a random process based on the binomial distribution.
21 entials, EPPs) is well described by a simple binomial distribution.
22 ed by Sr(2+) were best described as a simple binomial distribution.
23 etermined by the normal approximation to the binomial distribution.
24 culated with the normal approximation to the binomial distribution.
25 mer, which is in agreement with the expected binomial distribution.
26 osthospitalization prevalence using Bayesian binomial distributions.
27 on the translation of rate comparison to two binomial distributions.
29 sed linear model with an underlying negative binomial distribution, adjusted for sex, baseline number
30 individual molecules are counted based on a binomial distribution analysis of emission events detect
31 dure for power estimation using the negative binomial distribution and assuming a generalized linear
33 bles regression model that uses the negative binomial distribution and draws inference using a parame
34 CANOES models read counts using a negative binomial distribution and estimates variance of the read
35 o extend the methods to accommodate negative binomial distribution and implemented these tests in a n
37 and generalized linear models with negative binomial distribution and log-link function to examine t
38 ighted random-intercept models with negative binomial distribution and logistic-regression models to
39 eneralised estimating equation models with a binomial distribution and logit link function investigat
40 simulation experiments based on the negative binomial distribution and our proposed nonparametric sim
41 eudo-inferential' replicates from a negative binomial distribution and propose a general procedure fo
42 terpretation for features using a correlated binomial distribution and scales efficiently to analyze
43 ome among biological samples with a negative binomial distribution and uses a local variance estimati
44 generalized linear mixed-effects models with binomial distributions and log link fit to patient-level
45 oising data using the zero-inflated negative binomial distribution, and data enhancement through a di
46 pression in RNA-seq data based on a negative binomial distribution, and in paired data based on a bet
47 cell-free HIV-1 infection follows a negative-binomial distribution, and our model reproduces these da
49 er estimates from the zero-inflated negative binomial distribution are an unreliable indicator of zer
53 ed generalized logistic, gamma, and negative binomial distributions as models for compound behavior.
54 igher masses until they reached the expected binomial distribution at equilibrium after approximately
55 tion data that may not fully follow negative binomial distributions but rather more general mixture d
56 e alternative scenarios was calculated for a binomial distribution by considering currently observed
58 ne expression analysis based on the negative binomial distribution (DESeq) or Empirical analysis of D
60 delling of scRNAseq data based on a negative binomial distribution enhances shrinkage performance in
61 of a stable label in precursors following a binomial distribution, estimates depend on the inverse c
62 d points and a generalized linear model with binomial distribution for binary end points, with adjust
63 s, spatial power spectra, and deviation from binomial distribution for C + G% in large moving windows
65 ty is tested for each codon site, assuming a binomial distribution for the probability of obtaining c
69 (end-plate potentials, EPPs) follow a simple binomial distribution in both Ca(2+) and Sr(2+) solution
72 ollowed a beta-binomial rather than a simple binomial distribution, indicating that each family may h
75 parameter [Formula: see text] of a negative-binomial distribution is estimated at 0.06 and 0.2 for J
76 ve a closer to fit to data than the negative binomial distribution, it is consistently outperformed b
78 ast such an evaluation was performed using a binomial distribution model equation, which is inappropr
83 lets in the mass spectrum resulting from the binomial distribution of isotopic label in the bis-DNP d
84 activity of these proteins is described by a binomial distribution of proteins on transcripts contain
86 ng generalized linear models with a negative binomial distribution on the preceding 4 years of data a
87 n interaction matrix that follows a negative binomial distribution or general mixture distribution.
89 ctivity was recovered (theoretical 25% for a binomial distribution), proving that the functional unit
90 covering the IP samples only with 2 negative binomial distributions, QNB is based on 4 independent ne
92 logues in the 95%(13)C extracts, follows the binomial distribution, showing mirrored peak pairs for t
94 with being drawn from an underlying negative binomial distribution than either a log-normal distribut
95 ditive model framework based on the negative binomial distribution that allows flexible inference of
96 propose a new statistical tool based on beta-binomial distributions that can construct robust gene co
97 d retention in the mother cell) according to binomial distribution, thus limiting equal segregation o
98 kelihood function based on an over-dispersed binomial distribution to aggregate evidence for allelic
99 S assumed to be uncorrelated, we adopted the binomial distribution to approximate the statistical sig
100 and brings them together under a correlated binomial distribution to create an efficient hypothesis
102 empirical Bayesian method based on the beta-binomial distribution to model paired data from high-thr
103 edgeR pioneered the use of the negative binomial distribution to model read count data with repl
105 imating equations with binomial and negative binomial distributions to evaluate associations between
106 sing an existing model (based on Poisson and binomial distributions) to derive an expression for the
107 assessed by using the Student t test, exact binomial distribution, two-sample test of proportions, a
108 a likelihood function based on the negative binomial distribution, use a regularization approach to
110 incidence estimates were computed assuming a binomial distribution using the Wilson score method.
112 s in the data, a single GAM using a negative binomial distribution was suitable to make predictions o
113 ized estimating equations (GEE) model with a binomial distribution was used to assess covariates asso
117 k with non-informative priors and a negative binomial distribution, we projected [Formula: see text]
120 xed-effects generalized linear models with a binomial distribution were used to compare outcomes betw
121 zed estimating equations assuming a negative binomial distribution were used to estimate relative rat
122 eneralized estimating equation models with a binomial distribution were used to study longitudinal as
124 on may not be as appropriate as the negative binomial distribution when biological replicates are ava
125 urrent densities that approached a predicted binomial distribution where mutant and wild-type subunit
126 particular, we consider weights based on the binomial distribution, where the median of the p-values
127 seq data by sex revealed underlying negative binomial distributions which increased statistical power
128 d these with an approximation of the Poisson binomial distribution, which assigns partial incidence t
129 RISPRBetaBinomial or CB(2) Based on the beta-binomial distribution, which is better suited to sgRNA d
130 d on statistical models such as the negative binomial distribution, which is employed by the tools ed
131 consistent with both log-normal and negative binomial distributions, while the mean-variance relation
132 yzed as prevalence ratios calculated using a binomial distribution with a log link or robust Poisson
133 over a distance d can then be described by a binomial distribution with a standard deviation 0.5 x d1
135 ralized linear mixed model assuming negative binomial distribution with log link function on 3-time r
136 major-component distribution is similar to a binomial distribution with low error and low reference b
137 vision is random and asymmetric, following a binomial distribution with mean probability of 0.52-0.72
138 ring self-pollination in pea conforms to the binomial distribution with no evidence of a tetrad-polle
139 istribution of DCV displacements fits a beta-binomial distribution with the mean and the variance fol
140 ses following either the Poisson or negative binomial distribution with the rate parameter allowed to
141 e distribution should follow a beta-negative binomial distribution with the same parameters as the DC
142 ions, QNB is based on 4 independent negative binomial distributions with their variances and means li
143 gated whether offspring sex follows a simple binomial distribution within families and identified mat
144 is and compare the performance of three, the binomial distribution, z scores, and gene set enrichment