Showing 200 of total 627 results (show query)

r-lib

ps:List, Query, Manipulate System Processes

List, query and manipulate all system processes, on 'Windows', 'Linux' and 'macOS'.

Maintained by Gábor Csárdi. Last updated 17 days ago.

7.0 match 79 stars 15.09 score 108 scripts 1.5k dependents

bioc

graph:graph: A package to handle graph data structures

A package that implements some simple graph handling capabilities.

Maintained by Bioconductor Package Maintainer. Last updated 11 days ago.

graphandnetwork

5.3 match 11.78 score 764 scripts 342 dependents

welch-lab

cytosignal:What the Package Does (One Line, Title Case)

What the package does (one paragraph).

Maintained by Jialin Liu. Last updated 6 days ago.

openblascpp

6.3 match 16 stars 5.95 score 6 scripts

branchlab

metasnf:Meta Clustering with Similarity Network Fusion

Framework to facilitate patient subtyping with similarity network fusion and meta clustering. The similarity network fusion (SNF) algorithm was introduced by Wang et al. (2014) in <doi:10.1038/nmeth.2810>. SNF is a data integration approach that can transform high-dimensional and diverse data types into a single similarity network suitable for clustering with minimal loss of information from each initial data source. The meta clustering approach was introduced by Caruana et al. (2006) in <doi:10.1109/ICDM.2006.103>. Meta clustering involves generating a wide range of cluster solutions by adjusting clustering hyperparameters, then clustering the solutions themselves into a manageable number of qualitatively similar solutions, and finally characterizing representative solutions to find ones that are best for the user's specific context. This package provides a framework to easily transform multi-modal data into a wide range of similarity network fusion-derived cluster solutions as well as to visualize, characterize, and validate those solutions. Core package functionality includes easy customization of distance metrics, clustering algorithms, and SNF hyperparameters to generate diverse clustering solutions; calculation and plotting of associations between features, between patients, and between cluster solutions; and standard cluster validation approaches including resampled measures of cluster stability, standard metrics of cluster quality, and label propagation to evaluate generalizability in unseen data. Associated vignettes guide the user through using the package to identify patient subtypes while adhering to best practices for unsupervised learning.

Maintained by Prashanth S Velayudhan. Last updated 5 days ago.

bioinformaticsclusteringmetaclusteringsnf

4.5 match 8 stars 8.21 score 30 scripts

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.

3.5 match 7 stars 9.11 score 1.3k scripts 6 dependents

joshuaulrich

quantmod:Quantitative Financial Modelling Framework

Specify, build, trade, and analyse quantitative financial trading strategies.

Maintained by Joshua M. Ulrich. Last updated 14 days ago.

algorithmic-tradingchartingdata-importfinancetime-series

1.9 match 839 stars 16.17 score 8.1k scripts 343 dependents

guenardg

MPSEM:Modelling Phylogenetic Signals using Eigenvector Maps

Computational tools to represent phylogenetic signals using adapted eigenvector maps.

Maintained by Guillaume Guénard. Last updated 6 months ago.

5.2 match 4.80 score 21 scripts 1 dependents

lcrawlab

mvMAPIT:Multivariate Genome Wide Marginal Epistasis Test

Epistasis, commonly defined as the interaction between genetic loci, is known to play an important role in the phenotypic variation of complex traits. As a result, many statistical methods have been developed to identify genetic variants that are involved in epistasis, and nearly all of these approaches carry out this task by focusing on analyzing one trait at a time. Previous studies have shown that jointly modeling multiple phenotypes can often dramatically increase statistical power for association mapping. In this package, we present the 'multivariate MArginal ePIstasis Test' ('mvMAPIT') – a multi-outcome generalization of a recently proposed epistatic detection method which seeks to detect marginal epistasis or the combined pairwise interaction effects between a given variant and all other variants. By searching for marginal epistatic effects, one can identify genetic variants that are involved in epistasis without the need to identify the exact partners with which the variants interact – thus, potentially alleviating much of the statistical and computational burden associated with conventional explicit search based methods. Our proposed 'mvMAPIT' builds upon this strategy by taking advantage of correlation structure between traits to improve the identification of variants involved in epistasis. We formulate 'mvMAPIT' as a multivariate linear mixed model and develop a multi-trait variance component estimation algorithm for efficient parameter inference and P-value computation. Together with reasonable model approximations, our proposed approach is scalable to moderately sized genome-wide association studies. Crawford et al. (2017) <doi:10.1371/journal.pgen.1006869>. Stamp et al. (2023) <doi:10.1093/g3journal/jkad118>.

Maintained by Julian Stamp. Last updated 5 months ago.

cppepistasisepistasis-analysisgwasgwas-toolslinear-mixed-modelsmapitmvmapitvariance-componentsopenblascppopenmp

2.8 match 11 stars 6.90 score 17 scripts 1 dependents