Improved dynamic predictions from joint models of longitudinal and survival data with time-varying effects using P-splines.

abstract：:ChIP-chip (or ChIP-on-chip) is a technology for isolation and identification of genomic sites occupied by specific DNA-binding proteins in living cells. The ChIP-chip signals can be obtained over the whole genome by tiling arrays, where a peak shape is generally observed around a protein-binding site. In this article,...

journal_title：Biometrics

authors： Zheng M,Barrera LO,Ren B,Wu YN

更新日期：2007-09-01 00:00:00

abstract：:Statistical inference based on right-censored data for the proportional hazards (PH) model with missing covariates has received considerable attention, but interval-censored or current status data with missing covariates has not yet been investigated. Our study is partly motivated by the analysis of fracture data from...

journal_title：Biometrics

authors： Wen CC,Lin CT

更新日期：2011-09-01 00:00:00

abstract：:The fitting of finite mixture models via the EM algorithm is considered for data which are available only in grouped form and which may also be truncated. A practical example is presented where a mixture of two doubly truncated log-normal distributions is adopted to model the distribution of the volume of red blood ce...

journal_title：Biometrics

authors： McLachlan GJ,Jones PN

更新日期：1988-06-01 00:00:00

abstract：:A full-likelihood procedure is proposed for analyzing correlated binary data under the assumption of exchangeability. The binomial and beta-binomial models are shown to occur as special cases correspondingly, respectively, to the choice of degenerate and beta-mixing distributions. For a finite exchangeable binary sequ...

journal_title：Biometrics

authors： George EO,Bowman D

更新日期：1995-06-01 00:00:00

abstract：:Morrissey and Spiegelman (1999, Biometrics 55, 338 344) provided a comparative study of adjustment methods for exposure misclassification in case-control studies equipped with an internal validation sample. In addition to the maximum likelihood (ML) approach, they considered two intuitive procedures based on proposals...

journal_title：Biometrics

authors： Lyles RH

更新日期：2002-12-01 00:00:00

abstract：:We present a method for individual and integrative analysis of high dimension, low sample size data that capitalizes on the recurring theme in multivariate analysis of projecting higher dimensional data onto a few meaningful directions that are solutions to a generalized eigenvalue problem. We propose a general framew...

journal_title：Biometrics

authors： Safo SE,Ahn J,Jeon Y,Jung S

更新日期：2018-12-01 00:00:00

abstract：:We propose a likelihood-based test for comparing the means of two or more log-normal distributions, with possibly unequal variances. A modification to the likelihood ratio test is needed when sample sizes are small. The performance of the proposed procedures is compared with the F-ratio test using Monte Carlo simulati...

journal_title：Biometrics

authors： Gill PS

更新日期：2004-06-01 00:00:00

abstract：:Estimation of treatment effects in randomized studies is often hampered by possible selection bias induced by conditioning on or adjusting for a variable measured post-randomization. One approach to obviate such selection bias is to consider inference about treatment effects within principal strata, that is, principal...

journal_title：Biometrics

authors： Long DM,Hudgens MG

更新日期：2013-12-01 00:00:00

abstract：:The distance between homologous DNA sequences of two species is proposed to be -1/4 ln[det(P)], where P is the conditional probability matrix specifying the proportions of the various nucleotides in the second sequence, corresponding to each of the four nucleotides in the first sequence. A probability model is describ...

journal_title：Biometrics

authors： Barry D,Hartigan JA

更新日期：1987-06-01 00:00:00

abstract：:We propose group sequential tests of the equivalence of two treatments based on ideas related to repeated confidence intervals. These tests adapt readily to unpredictable group sizes, to the possibility of continuing even though a boundary has been crossed, and to nonnormal observations. In comparing two binomial dist...

journal_title：Biometrics

authors： Jennison C,Turnbull BW

更新日期：1993-03-01 00:00:00

abstract：:In family studies, canonical discriminant analysis can be used to find linear combinations of phenotypes that exhibit high ratios of between-family to within-family variabilities. But with large numbers of phenotypes, canonical discriminant analysis may overfit. To estimate the predicted ratios associated with the coe...

journal_title：Biometrics

authors： Jin M,Fang Y

更新日期：2011-03-01 00:00:00

abstract：:In controlled clinical trials there are usually several prognostic factors known or thought to influence the patient's ability to respond to treatment. Therefore, the method of sequential treatment assignment needs to be designed so that treatment balance is simultaneously achieved across all such patients factor. Tra...

journal_title：Biometrics

authors： Pocock SJ,Simon R

更新日期：1975-03-01 00:00:00

abstract：:Some failure time data come from a population that consists of some subjects who are susceptible to and others who are nonsusceptible to the event of interest. The data typically have heavy censoring at the end of the follow-up period, and a standard survival analysis would not always be appropriate. In such situation...

journal_title：Biometrics

authors： Sy JP,Taylor JM

更新日期：2000-03-01 00:00:00

abstract：:We develop a parameterization of the beta-binomial mixture that provides sensible inferences about the size of a closed population when probabilities of capture or detection vary among individuals. Three classes of mixture models (beta-binomial, logistic-normal, and latent-class) are fitted to recaptures of snowshoe h...

journal_title：Biometrics

authors： Dorazio RM,Royle JA

更新日期：2003-06-01 00:00:00

abstract：:Let Yi be an ni X 1 vector of observations, Xi an ni X p matrix of known values, and beta an unknown p X 1 with the structure Yi = Xi beta + epsilon i, where the covariance matrix of epsilon i is of intra-class form, that is Cov (epsilon i) = sigma2[(1 - rho) Ii + rho e i e i'] where Ii is the ni X ni identity matrix ...

journal_title：Biometrics

authors： Wiorkowski JJ

更新日期：1975-09-01 00:00:00

abstract：:Ophthalmologic studies often compare several groups of subjects for the presence or absence of some ocular finding, where each subject may contribute two eyes to the analysis, the values from the two eyes being highly correlated. Rosner (1982, Biometrics 38, 105-114) and Dallal (1988, Biometrics 44, 253-257) proposed ...

journal_title：Biometrics

authors： Donner A

更新日期：1989-06-01 00:00:00

abstract：:Often with data from immunoassays, the concentration-response relationship is nonlinear and intra-assay response variance is heterogeneous. Estimation of the standard curve is usually based on a nonlinear heteroscedastic regression model for concentration-response, where variance is modeled as a function of mean respo...

journal_title：Biometrics

authors： Belanger BA,Davidian M,Giltinan DM

更新日期：1996-03-01 00:00:00

abstract：:Traditional studies of short-term air pollution health effects use time series data, while cohort studies generally focus on long-term effects. There is increasing interest in exploiting individual level cohort data to assess short-term health effects in order to understand the mechanisms and time scales of action. We...

journal_title：Biometrics

authors： Szpiro AA,Sheppard L,Adar SD,Kaufman JD

更新日期：2014-03-01 00:00:00

abstract：:Asbestos exposure is a well-known risk factor for various lung diseases, and when they occur, workmen's compensation boards need to make decisions concerning the probability the cause is work related. In the absence of a definitive work history, measures of short and long asbestos fibers as well as counts of asbestos ...

journal_title：Biometrics

authors： Weichenthal S,Joseph L,Bélisle P,Dufresne A

更新日期：2010-06-01 00:00:00

abstract：:Estimating the number of clusters in a data set is a crucial step in cluster analysis. In this article, motivated by the gap method (Tibshirani, Walther, and Hastie, 2001, Journal of the Royal Statistical Society B63, 411-423), we propose the weighted gap and the difference of difference-weighted (DD-weighted) gap met...

journal_title：Biometrics

authors： Yan M,Ye K

更新日期：2007-12-01 00:00:00

abstract：:Tsiatis, Rosner, and Mehta (1984, Biometrics 40, 797-803) proposed a procedure for constructing confidence intervals following group sequential tests of a normal mean. This method is first extended for group sequential tests for which the sample sizes between interim analyses are not identical or the times are not equ...

journal_title：Biometrics

authors： Kim K,DeMets DL

更新日期：1987-12-01 00:00:00

abstract：:Capture-recapture models were originally developed to account for encounter probabilities that are less than 1 in free-ranging animal populations. Nowadays, these models can deal with the movement of animals between different locations and are also used to study transitions between different states. However, their use...

journal_title：Biometrics

authors： Pradel R

更新日期：2005-06-01 00:00:00

abstract：:Certain probability models sometimes provide poor descriptions when fitted to data by maximum likelihood. We examine one such model for the survival of wild animals, which is fitted to two sets of data. When the model behaves poorly, its expected information matrix, evaluated at the maximum likelihood estimate of para...

journal_title：Biometrics

authors： Catchpole EA,Kgosi PM,Morgan BJ

更新日期：2001-09-01 00:00:00

abstract：:Some covariate-adaptive randomization methods have been used in clinical trials for a long time, but little theoretical work has been done about testing hypotheses under covariate-adaptive randomization until Shao et al. (2010) who provided a theory with detailed discussion for responses under linear models. In this a...

journal_title：Biometrics

authors： Shao J,Yu X

更新日期：2013-12-01 00:00:00

abstract：:Brain evoked potential (EP) data consist of a true response ("signal") and random background activity ("noise"), which are observed over repeated stimulus presentations ("trials"). A signal that changes slowly from trial to trial can be estimated by smoothing across trials and over time within trials. We present a met...

journal_title：Biometrics

authors： Raz J,Turetsky B,Fein G

更新日期：1989-09-01 00:00:00

abstract：:In an analysis of capture-recapture data, the identification of a model that fits is a critical step. For the multisite (also called multistate) models used to analyze data gathered at several sites, no reliable test for assessing fit is currently available. We propose a test for the JMV model, a simple generalization...

journal_title：Biometrics

authors： Pradel R,Wintrebert CM,Gimenez O

更新日期：2003-03-01 00:00:00

abstract：:The Colton model for the choice between two medical treatments is studied, with the additional assumption that there is a time lag between the administration of the treatments and the availability of the responses. Two simple procedures are suggested for dealing with patients who arrive during the waiting period, caus...

journal_title：Biometrics

authors： Langenberg P,Srinivasan R

更新日期：1981-03-01 00:00:00

abstract：:The basic problem under consideration is the comparison of treatments with respect to a response Y when a covariable X is taken into account. Various methods involving matching may be regarded as compromises between the standard analysis of covariance and the standard analysis of independent matched pairs. First, ther...

journal_title：Biometrics

authors： Quade D

更新日期：1982-09-01 00:00:00

abstract：:In multivariate survival analysis, investigators are often interested in testing for heterogeneity among clusters, both overall and within specific classes. We represent different hypotheses about the heterogeneity structure using a sequence of gamma frailty models, ranging from a null model with no random effects to ...

journal_title：Biometrics

authors： Dunson DB,Chen Z

更新日期：2004-06-01 00:00:00

abstract：:This paper proposes a two-stage phase I-II clinical trial design to optimize dose-schedule regimes of an experimental agent within ordered disease subgroups in terms of the toxicity-efficacy trade-off. The design is motivated by settings where prior biological information indicates it is certain that efficacy will imp...

journal_title：Biometrics

authors： Lin R,Thall PF,Yuan Y

更新日期：2020-03-01 00:00:00