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Downloading, Reading and Analyzing PNADC Microdata
Provides tools for downloading, reading and analyzing the Continuous National Household Sample Survey - PNADC, a household survey from Brazilian Institute of Geography and Statistics - IBGE. The data must be downloaded from the official website < https://www.ibge.gov.br/>. Further analysis must be made using package 'survey'.
Sample Size for SMART Designs in Non-Surgical Periodontal Trials
Sample size calculation to detect dynamic treatment regime (DTR) effects based on change in clinical attachment level (CAL) outcomes from a non-surgical chronic periodontitis treatments study. The experiment is performed under a Sequential Multiple Assignment Randomized Trial (SMART) design. The clustered tooth (sub-unit) level CAL outcomes are skewed, spatially-referenced, and non-randomly missing. The implemented algorithm is available in Xu et al. (2019+)
A Distributed Worker Launcher Framework
In computationally demanding analysis projects,
statisticians and data scientists asynchronously
deploy long-running tasks to distributed systems,
ranging from traditional clusters to cloud services.
The 'NNG'-powered 'mirai' R package by Gao (2023)
Reference Limits using QQ Methodology
A collection of routines for finding reference limits using, where
appropriate, QQ methodology. All use a data vector X of cases from the
reference population. The default is to get the central 95% reference range
of the population, namely the 2.5 and 97.5 percentile, with optional
adjustment of the range. Along with the reference limits, we want
confidence intervals which, for historical reasons, are typically at 90%
confidence. A full analysis provides six numbers:
– the upper and the lower reference limits, and
- each of their confidence intervals.
For application details, see Hawkins and Esquivel (2024)
Data sets from "Introductory Statistics for Engineering Experimentation"
Datasets from Nelson, Coffin and Copeland "Introductory Statistics for Engineering Experimentation" (Elsevier, 2003) with sample code.
Cohen's D_p Computation with Confidence Intervals
Computing Cohen's d_p in any experimental designs (between-subject, within-subject, and single-group design). Cousineau (2022) < https://github.com/dcousin3/CohensdpLibrary>; Cohen (1969, ISBN: 0-8058-0283-5).
Advanced Processing and Chart Generation from activPAL Events Files
Contains functions to generate pre-defined summary statistics from activPAL events files < https://www.palt.com/>. The package also contains functions to produce informative graphics that visualise physical activity behaviour and trends. This includes generating graphs that align physical activity behaviour with additional time based observations described by other data sets, such as sleep diaries and continuous glucose monitoring data.
Precision Profile Weighted Deming Regression
Weighted Deming regression, also known as 'errors-in-variable'
regression, is applied with suitable weights. Weights are modeled via a
precision profile; thus the methods implemented here are referred to as
precision profile weighted Deming (PWD) regression. The package covers
two settings – one where the precision profiles are known either from
external studies or from adequate replication of the X and Y readings,
and one in which there is a plausible functional form for the precision
profiles but the exact (unknown) function must be estimated from the
(generally singlicate) readings.
The function set includes tools for: estimated standard errors (via
jackknifing); standardized-residual analysis function with regression
diagnostic tools for normality, linearity and constant variance; and an
outlier analysis identifying significant outliers for closer investigation.
The following reference provides further information on mathematical
derivations and applications.
Hawkins, D.M., and J.J. Kraker (2026). 'Precision Profile Weighted
Deming Regression for Methods Comparison'.
The Journal of Applied Laboratory Medicine 11, 379-392
Inferring Differentially Expressed Genes using Generalized Linear Mixed Models
Genes that are differentially expressed between two or more experimental conditions can be detected in RNA-Seq. A high biological variability may impact the discovery of these genes once it may be divergent between the fixed effects. However, this variability can be covered by the random effects. 'DEGRE' was designed to identify the differentially expressed genes considering fixed and random effects on individuals. These effects are identified earlier in the experimental design matrix. 'DEGRE' has the implementation of preprocessing procedures to clean the near zero gene reads in the count matrix, normalize by 'RLE' published in the 'DESeq2' package, 'Love et al. (2014)'
Nonparametric Methods for Cognitive Diagnosis
An array of nonparametric and parametric estimation methods for cognitive diagnostic models, including nonparametric classification of examinee attribute profiles, joint maximum likelihood estimation (JMLE) of examinee attribute profiles and item parameters, and nonparametric refinement of the Q-matrix, as well as conditional maximum likelihood estimation (CMLE) of examinee attribute profiles given item parameters and CMLE of item parameters given examinee attribute profiles. Currently the nonparametric methods in the package support both conjunctive and disjunctive models, and the parametric methods in the package support the DINA model, the DINO model, the NIDA model, the G-NIDA model, and the R-RUM model.