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Topic > Genetics
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12 projects in result set.
0. umx: A helper library for SEM in OpenMx - umx provides functions making it easy to build, run, modify, and report the results of Structural Equation Models (SEM) using OpenMx. Examples include setting start values: umxStart(); labels: umxLabel(); and reporting; umxSummary(). | |
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Activity Percentile: 0.00 Registered: 2013-08-28 13:52 |
1. genoPlotR - plot gene and genome maps - genoPlotR is a R package to produce reproducible, publication-grade graphics of gene and genome maps. It allows the user to read from usual format such as protein table files and blast results, as well as home-made tabular files. | |
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Activity Percentile: 0.00 Registered: 2010-01-08 16:59 |
2. GWAtoolbox - An R-package implemented for genome-wide association studies. The main feature is very vast quality check of data before meta-analysis. It provides an extensive list of quality statistics presented using easy-to-use DHTML and graphical outputs. | |
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Activity Percentile: 0.00 Registered: 2011-03-23 10:20 |
3. LazyMLVA - This project automates assignment of MLVA (Multiple locus VNTR (Variable-Number-of-Tandem-Repeats) Analysis) types from files straight out of the sequencer. | |
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Activity Percentile: 0.00 Registered: 2010-01-08 10:31 |
4. aroma.* packages [MOVED TO GITHUB] - This repository and all of its packages have been moved to https://github.com/HenrikBengtsson/ | |
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Activity Percentile: 0.00 Registered: 2009-05-19 20:01 |
5. cgen - Parallel Genomic Prediction and GWAS in R using Eigen and Rcpp | |
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Activity Percentile: 0.00 Registered: 2013-05-29 18:34 |
6. sonicLength - sonicLength estimates the abundances of cells marked with integrated DNA using DNA fragment length data. Also included are tools for random number generation apropos to fragment lengths, simulating datasets, and jackknifing multiple replicates | |
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Activity Percentile: 0.00 Registered: 2011-09-14 03:27 |
7. Sublogo dendrograms - Sublogo dendrograms are statistical graphics that reveal correlation in biological sequence alignments. | |
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Registered: 2009-06-19 09:14 |
8. CNVScope - CNVScope: Visually exploring copy number aberrations in
cancer genomes | |
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Activity Percentile: 0.00 Registered: 2019-07-16 15:34 |
9. Genome-wide analysis using MOSS - Performs genome-wide analysis of dense SNP array data using the mode oriented stochastic search (MOSS) algorithm in a case-control design. Includes preprocessing of the data from Plink format to the format required by the MOSS algorithm. | |
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Activity Percentile: 0.00 Registered: 2011-01-07 17:53 |
10. Benchmarking genomic data integration - Comparison pipeline for multi-platform data integration algorithms for functional genomics studies. Provides tools to compare performance between publicly available implementations | |
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Activity Percentile: 0.00 Registered: 2011-02-02 00:51 |
11. casper - casper infers alternative splicing from high-throughput sequencing data both for known variants and de novo discovery. We use a Bayesian model with few assumptions, and modern model selection ideas with improved theoretical and computational properties. | |
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Activity Percentile: 0.00 Registered: 2011-10-11 08:51 |