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One key exploratory analysis step in single-cell genomics data analysis is the prediction of features with different activity levels. For example, we want to predict differentially expressed genes (DEGs) in single-cell RNA-seq data, spatial DEGs in spatial transcriptomics data, or differentially accessible regions (DARs) in single-cell ATAC-seq data. singleCellHaystack predicts differentially active features in single cell omics datasets without relying on the clustering of cells into arbitrary clusters. singleCellHaystack uses Kullback-Leibler divergence to find features (e.g., genes, genomic regions, etc) that are active in subsets of cells that are non-randomly positioned inside an input space (such as 1D trajectories, 2D tissue sections, multi-dimensional embeddings, etc). For the theoretical background of singleCellHaystack we refer to our original paper Vandenbon and Diez (Nature Communications, 2020) <doi:10.1038/s41467-020-17900-3> and our update Vandenbon and Diez (Scientific Reports, 2023) <doi:10.1038/s41598-023-38965-2>.
The overall performance of soil ecosystem services and productivity greatly relies on soil health, making it a crucial indicator. The evaluation of soil physical, chemical, and biological parameters is necessary to determine the overall soil quality index. In our package, three commonly used methods, including linear scoring, regression-based, and principal component-based soil quality indexing, are employed to calculate the soil quality index. This package has been developed using concept of Bastida et al. (2008) and Doran and Parkin (1994) <doi:10.1016/j.geoderma.2008.08.007> <doi:10.2136/sssaspecpub35.c1>.
Fit design-based linear and logistic elastic nets with complex survey data considering the sampling design when defining training and test sets using replicate weights. Methods implemented in this package are described in: A. Iparragirre, T. Lumley, I. Barrio, I. Arostegui (2024) <doi:10.1002/sta4.578>.
This package provides a tool for survival analysis using a discrete time approach with ensemble binary classification. spect provides a simple interface consistent with commonly used R data analysis packages, such as caret', a variety of parameter options to help facilitate search automation, a high degree of transparency to the end-user - all intermediate data sets and parameters are made available for further analysis and useful, out-of-the-box visualizations of model performance. Methods for transforming survival data into discrete-time are adapted from the autosurv package by Suresh et al., (2022) <doi:10.1186/s12874-022-01679-6>.
Detection of item-wise Differential Item Functioning (DIF) in fitted mirt', multipleGroup or bfactor models using score-based structural change tests. Under the hood the sctest() function from the strucchange package is used.
This package provides tools for calculating disclosure risk measures for microdata, including record-level and file-level measures. The record-level disclosure risk is estimated primarily using exhaustive tabulation. The file-level disclosure risk is estimated by fitting loglinear models on the observed sample counts in cells formed by key variables and their interactions. Funded by the National Center for Education Statistics. See Skinner and Shlomo (2008) <doi:10.1198/016214507000001328> for a description of the file-level risk measures and the loglinear model approach.
Sequences sampled at different time points can be used to infer molecular phylogenies on natural time scales, but if the sequences records inaccurate sampling times, that are not the actual sampling times, then it will affect the molecular phylogenetic analysis. This shiny application helps exploring temporal characteristics of the evolutionary trees through linear regression analysis and with the ability to identify and remove incorrect labels. The method was extended to support exploring other phylogenetic signals under strict and relaxed models.
Use R to interface with the Charles Schwab Trade API <https://developer.schwab.com/>. Functions include authentication, trading, price requests, account information, and option chains. A user will need a Schwab brokerage account and Schwab Individual Developer app. See README for authentication process and examples.
Performance of functional kriging, cokriging, optimal sampling and simulation for spatial prediction of functional data. The framework of spatial prediction, optimal sampling and simulation are extended from scalar to functional data. SpatFD is based on the Karhunen-Loève expansion that allows to represent the observed functions in terms of its empirical functional principal components. Based on this approach, the functional auto-covariances and cross-covariances required for spatial functional predictions and optimal sampling, are completely determined by the sum of the spatial auto-covariances and cross-covariances of the respective score components. The package provides new classes of data and functions for modeling spatial dependence structure among curves. The spatial prediction of curves at unsampled locations can be carried out using two types of predictors, and both of them report, the respective variances of the prediction error. In addition, there is a function for the determination of spatial locations sampling configuration that ensures minimum variance of spatial functional prediction. There are also two functions for plotting predicted curves at each location and mapping the surface at each time point, respectively. References Bohorquez, M., Giraldo, R., and Mateu, J. (2016) <doi:10.1007/s10260-015-0340-9>, Bohorquez, M., Giraldo, R., and Mateu, J. (2016) <doi:10.1007/s00477-016-1266-y>, Bohorquez M., Giraldo R. and Mateu J. (2021) <doi:10.1002/9781119387916>.
Smart Adaptive Recommendations (SAR) is the name of a fast, scalable, adaptive algorithm for personalized recommendations based on user transactions and item descriptions. It produces easily explainable/interpretable recommendations and handles "cold item" and "semi-cold user" scenarios. This package provides two implementations of SAR': a standalone implementation, and an interface to a web service in Microsoft's Azure cloud: <https://github.com/Microsoft/Product-Recommendations/blob/master/doc/sar.md>. The former allows fast and easy experimentation, and the latter provides robust scalability and extra features for production use.
This package provides flexible hazard ratio curves allowing non-linear relationships between continuous predictors and survival. To better understand the effects that each continuous covariate has on the outcome, results are expressed in terms of hazard ratio curves, taking a specific covariate value as reference. Confidence bands for these curves are also derived.
Create mocked bindings to Shiny update functions within test function calls to automatically update input values. The mocked bindings simulate the communication between the server and UI components of a Shiny module in testServer().
This package provides functions for fitting a sparse partial least squares (SPLS) regression and classification (Chun and Keles (2010) <doi:10.1111/j.1467-9868.2009.00723.x>).
Terrestrial and marine predictors for species distribution modelling from multiple sources, including WorldClim <https://www.worldclim.org/>,, ENVIREM <https://envirem.github.io/>, Bio-ORACLE <https://bio-oracle.org/> and MARSPEC <http://www.marspec.org/>.
Adds variable-selection functions for Beta regression models (both mean and phi submodels) so they can be used within the SelectBoost algorithm. Includes stepwise AIC, BIC, and corrected AIC on betareg() fits, gamlss'-based LASSO/Elastic-Net, a pure glmnet iterative re-weighted least squares-based selector with an optional standardization speedup, and C++ helpers for iterative re-weighted least squares working steps and precision updates. Also provides a fastboost_interval() variant for interval responses, comparison helpers, and a flexible simulator simulation_DATA.beta() for interval-valued data. For more details see Bertrand and Maumy (2023) <doi:10.7490/f1000research.1119552.1>.
Supports survey research workflows built around a typed instrument object (the sframe). Features include visual instrument design via a browser-based builder or Shiny studio, export to a self-contained static HTML survey, an embeddable Shiny module, SHA-256 integrity-checked serialisation to the .sframe format, multi-page survey rendering, branching logic, response quality checking, scale scoring, psychometric diagnostics, analysis-plan execution, model syntax planning, an interactive response dashboard, codebook generation, and reproducible HTML reporting.
The package performs a sensitivity analysis in an observational study using an M-statistic, for instance, the mean. The main function in the package is senmv(), but amplify() and truncatedP() are also useful. The method is developed in Rosenbaum Biometrics, 2007, 63, 456-464, <doi:10.1111/j.1541-0420.2006.00717.x>.
This package implements an approach aimed at assessing the accuracy and effectiveness of raw scores obtained in scales that contain locally dependent items. The program uses as input the calibration (structural) item estimates obtained from fitting extended unidimensional factor-analytic solutions in which the existing local dependencies are included. Measures of reliability (Omega) and information are proposed at three levels: (a) total score, (b) bivariate-doublet, and (c) item-by-item deletion, and are compared to those that would be obtained if all the items had been locally independent. All the implemented procedures can be obtained from: (a) linear factor-analytic solutions in which the item scores are treated as approximately continuous, and (b) non-linear solutions in which the item scores are treated as ordered-categorical. A detailed guide can be obtained at the following url.
Collection of datasets from Sen & Srivastava: "Regression Analysis, Theory, Methods and Applications", Springer. Sources for individual data files are more fully documented in the book.
This package provides an interface to shiny inputs used for filtering vectors, data.frames, and other objects. S7'-based implementation allows for seamless extensibility.
The objective of these functions is to derive a species assemblage that satisfies a functional trait profile. Restoring resilient ecosystems requires a flexible framework for selecting assemblages that are based on the functional traits of species. However, current trait-based models have been limited to algorithms that can only select species by optimising specific trait values, and could not elegantly accommodate the common desire among restoration ecologists to produce functionally diverse assemblages. We have solved this problem by applying a non-linear optimisation algorithm that optimises Rao Q, a closed-form functional trait diversity index that incorporates species abundances, subject to other linear constraints. This framework generalises previous models that only optimised the entropy of the community, and can optimise both functional diversity and entropy simultaneously. This package can also be used to generate experimental assemblages to test the effects of community-level traits on community dynamics and ecosystem function. The method is based on theory discussed in Laughlin (2014, Ecology Letters) and Laughlin et al. (2018, Methods in Ecology and Evolution).
Offers Bayesian semiparametric density estimation and tail-index estimation for heavy tailed data, by using a parametric, tail-respecting transformation of the data to the unit interval and then modeling the transformed data with a purely nonparametric logistic Gaussian process density prior. Based on Tokdar et al. (2022) <doi:10.1080/01621459.2022.2104727>.
Formulates a sparse distance weighted discrimination (SDWD) for high-dimensional classification and implements a very fast algorithm for computing its solution path with the L1, the elastic-net, and the adaptive elastic-net penalties. More details about the methodology SDWD is seen on Wang and Zou (2016) (<doi:10.1080/10618600.2015.1049700>).
RNA sequencing analysis methods are often derived by relying on hypothetical parametric models for read counts that are not likely to be precisely satisfied in practice. Methods are often tested by analyzing data that have been simulated according to the assumed model. This testing strategy can result in an overly optimistic view of the performance of an RNA-seq analysis method. We develop a data-based simulation algorithm for RNA-seq data. The vector of read counts simulated for a given experimental unit has a joint distribution that closely matches the distribution of a source RNA-seq dataset provided by the user. Users control the proportion of genes simulated to be differentially expressed (DE) and can provide a vector of weights to control the distribution of effect sizes. The algorithm requires a matrix of RNA-seq read counts with large sample sizes in at least two treatment groups. Many datasets are available that fit this standard.