Showing 136 of total 136 results (show query)

alanarnholt

BSDA:Basic Statistics and Data Analysis

Data sets for book "Basic Statistics and Data Analysis" by Larry J. Kitchens.

Maintained by Alan T. Arnholt. Last updated 2 years ago.

3.8 match 7 stars 9.11 score 1.3k scripts 6 dependents

reside-ic

ids:Generate Random Identifiers

Generate random or human readable and pronounceable identifiers.

Maintained by Rich FitzJohn. Last updated 3 years ago.

1.7 match 94 stars 13.27 score 175 scripts 165 dependents

mrc-ide

malariasimulation:An individual based model for malaria

Specifies the latest and greatest malaria model.

Maintained by Giovanni Charles. Last updated 27 days ago.

cpp

1.5 match 16 stars 8.17 score 146 scripts

mrc-ide

rrq:Simple Redis Queue

Simple Redis queue in R.

Maintained by Rich FitzJohn. Last updated 4 months ago.

clusterinfrastructure

1.6 match 24 stars 7.40 score 14 scripts 3 dependents

mrc-ide

context:Contexts for evaluating R expressions

Contexts for evaluating R expressions.

Maintained by Rich FitzJohn. Last updated 2 years ago.

clusterinfrastructure

1.7 match 5 stars 6.59 score 1.7k scripts 1 dependents

bioc

GeneOverlap:Test and visualize gene overlaps

Test two sets of gene lists and visualize the results.

Maintained by António Miguel de Jesus Domingues, Max-Planck Institute for Cell Biology and Genetics. Last updated 5 months ago.

multiplecomparisonvisualization

1.6 match 6.43 score 266 scripts

mrc-ide

hipercow:High Performance Computing

Set up cluster environments and jobs. Moo.

Maintained by Rich FitzJohn. Last updated 11 days ago.

1.6 match 1 stars 6.53 score 45 scripts 1 dependents

mrc-ide

odin2:Next generation odin

Temporary package for rewriting odin.

Maintained by Rich FitzJohn. Last updated 2 months ago.

1.6 match 5 stars 6.32 score 22 scripts

mrc-ide

didehpc:DIDE HPC Support

Previous DIDE HPC support. Don't use this, use hipercow instead.

Maintained by Rich FitzJohn. Last updated 4 months ago.

clusterinfrastructure

1.6 match 10 stars 3.94 score 58 scripts

joundso

cleaR:Clean the R Console and Environment

Small package to clean the R console and the R environment with the call of just one function.

Maintained by Jonathan M. Mang. Last updated 1 years ago.

1.6 match 3.78 score 3 scripts 4 dependents

mrc-ide

queuer:Queue Tasks

Queue tasks to number of backends.

Maintained by Rich FitzJohn. Last updated 2 years ago.

clusterinfrastructure

1.7 match 4 stars 2.78 score 4 scripts

mrc-ide

testthat.buildkite:A testthat reporter for buildkite

A testthat reporter that prints progress output in a format for use in buildkite logs.

Maintained by Robert Ashton. Last updated 2 years ago.

1.7 match 2.54 score 1 scripts

mrc-ide

conan2:Conan the Librarian

Create libraries. For us, there is no spring. Just the wind that smells fresh before the storm.

Maintained by Rich FitzJohn. Last updated 17 days ago.

1.7 match 2.48 score 1 scripts 1 dependents

mrc-ide

mode:Solve Multiple ODEs

Solve multiple ODEs in parallel.

Maintained by Rich FitzJohn. Last updated 2 years ago.

1.6 match 2.10 score 25 scripts

mrc-ide

orderly.sharedfile:Package Title Here

Access files in shared locations from orderly.

Maintained by Rich FitzJohn. Last updated 5 months ago.

1.7 match 1 stars 2.00 score 2 scripts

vimc

orderly.rstudio:RStudio addins for orderly

RStudio addins for orderly.

Maintained by Robert Ashton. Last updated 4 years ago.

1.7 match 1 stars 1.70 score 1 scripts

mjuraska

CoRpower:Power Calculations for Assessing Correlates of Risk in Clinical Efficacy Trials

Calculates power for assessment of intermediate biomarker responses as correlates of risk in the active treatment group in clinical efficacy trials, as described in Gilbert, Janes, and Huang, Power/Sample Size Calculations for Assessing Correlates of Risk in Clinical Efficacy Trials (2016, Statistics in Medicine). The methods differ from past approaches by accounting for the level of clinical treatment efficacy overall and in biomarker response subgroups, which enables the correlates of risk results to be interpreted in terms of potential correlates of efficacy/protection. The methods also account for inter-individual variability of the observed biomarker response that is not biologically relevant (e.g., due to technical measurement error of the laboratory assay used to measure the biomarker response), which is important because power to detect a specified correlate of risk effect size is heavily affected by the biomarker's measurement error. The methods can be used for a general binary clinical endpoint model with a univariate dichotomous, trichotomous, or continuous biomarker response measured in active treatment recipients at a fixed timepoint after randomization, with either case-cohort Bernoulli sampling or case-control without-replacement sampling of the biomarker (a baseline biomarker is handled as a trivial special case). In a specified two-group trial design, the computeN() function can initially be used for calculating additional requisite design parameters pertaining to the target population of active treatment recipients observed to be at risk at the biomarker sampling timepoint. Subsequently, the power calculation employs an inverse probability weighted logistic regression model fitted by the tps() function in the 'osDesign' package. Power results as well as the relationship between the correlate of risk effect size and treatment efficacy can be visualized using various plotting functions. To link power calculations for detecting a correlate of risk and a correlate of treatment efficacy, a baseline immunogenicity predictor (BIP) can be simulated according to a specified classification rule (for dichotomous or trichotomous BIPs) or correlation with the biomarker response (for continuous BIPs), then outputted along with biomarker response data under assignment to treatment, and clinical endpoint data for both treatment and placebo groups.

Maintained by Michal Juraska. Last updated 4 years ago.

0.5 match 4.15 score 14 scripts

tjk23

SuRF.vs:Subsampling Ranking Forward Selection (SuRF)

Performs variable selection based on subsampling, ranking forward selection. Details of the method are published in Lihui Liu, Hong Gu, Johan Van Limbergen, Toby Kenney (2020) SuRF: A new method for sparse variable selection, with application in microbiome data analysis Statistics in Medicine 40 897-919 <doi:10.1002/sim.8809>. Xo is the matrix of predictor variables. y is the response variable. Currently only binary responses using logistic regression are supported. X is a matrix of additional predictors which should be scaled to have sum 1 prior to analysis. fold is the number of folds for cross-validation. Alpha is the parameter for the elastic net method used in the subsampling procedure: the default value of 1 corresponds to LASSO. prop is the proportion of variables to remove in the each subsample. weights indicates whether observations should be weighted by class size. When the class sizes are unbalanced, weighting observations can improve results. B is the number of subsamples to use for ranking the variables. C is the number of permutations to use for estimating the critical value of the null distribution. If the 'doParallel' package is installed, the function can be run in parallel by setting ncores to the number of threads to use. If the default value of 1 is used, or if the 'doParallel' package is not installed, the function does not run in parallel. display.progress indicates whether the function should display messages indicating its progress. family is a family variable for the glm() fitting. Note that the 'glmnet' package does not permit the use of nonstandard link functions, so will always use the default link function. However, the glm() fitting will use the specified link. The default is binomial with logistic regression, because this is a common use case. pval is the p-value for inclusion of a variable in the model. Under the null case, the number of false positives will be geometrically distributed with this as probability of success, so if this parameter is set to p, the expected number of false positives should be p/(1-p).

Maintained by Toby Kenney. Last updated 3 years ago.

0.5 match 2.00 score 5 scripts