r-seqarray
|
1.44.0-1 |
0 |
0.00
|
Data management of large-scale whole-genome sequence variant calls |
BioArchLinuxBot
|
2024-05-02 00:09 (UTC) |
r-sepira
|
1.22.0-1 |
0 |
0.00
|
Systems EPigenomics Inference of Regulatory Activity |
BioArchLinuxBot
|
2024-04-13 18:02 (UTC) |
r-scmageck
|
1.9.1-4 |
0 |
0.00
|
Identify genes associated with multiple expression phenotypes in single-cell CRISPR screening data |
BioArchLinuxBot
|
2023-04-29 05:01 (UTC) |
r-scalign
|
1.12.0-4 |
0 |
0.00
|
An alignment and integration method for single cell genomics |
BioArchLinuxBot
|
2023-04-29 05:24 (UTC) |
r-saigegds
|
2.4.0-1 |
0 |
0.00
|
Scalable Implementation of Generalized mixed models using GDS files in Phenome-Wide Association Studies |
BioArchLinuxBot
|
2024-05-10 12:02 (UTC) |
r-rtracklayer
|
1.64.0-1 |
0 |
0.00
|
R interface to genome annotation files and the UCSC genome browser |
BioArchLinuxBot
|
2024-05-02 23:36 (UTC) |
r-rtopper
|
1.50.0-1 |
0 |
0.00
|
This package is designed to perform Gene Set Analysis across multiple genomic platforms |
BioArchLinuxBot
|
2024-05-01 18:40 (UTC) |
r-rtcga
|
1.34.0-1 |
0 |
0.00
|
The Cancer Genome Atlas Data Integration |
BioArchLinuxBot
|
2024-05-01 21:11 (UTC) |
r-rlmm
|
1.66.0-1 |
0 |
0.00
|
A Genotype Calling Algorithm for Affymetrix SNP Arrays |
BioArchLinuxBot
|
2024-05-02 04:16 (UTC) |
r-rjmcmcnucleosomes
|
1.28.0-1 |
0 |
0.00
|
Bayesian hierarchical model for genome-wide nucleosome positioning with high-throughput short-read data (MNase-Seq) |
BioArchLinuxBot
|
2024-05-03 03:40 (UTC) |
r-ribocrypt
|
1.10.0-1 |
0 |
0.00
|
Interactive visualization in genomics |
BioArchLinuxBot
|
2024-05-03 18:40 (UTC) |
r-rgmql
|
1.24.0-1 |
0 |
0.00
|
GenoMetric Query Language for R/Bioconductor |
BioArchLinuxBot
|
2024-05-03 01:12 (UTC) |
r-rgenometracksdata
|
0.99.0-4 |
0 |
0.00
|
Demonstration Data from rGenomeTracks Package |
BioArchLinuxBot
|
2022-06-06 12:39 (UTC) |
r-rgenometracks
|
1.10.0-1 |
0 |
0.00
|
Integerated visualization of epigenomic data |
BioArchLinuxBot
|
2024-05-02 02:17 (UTC) |
r-resolve
|
1.6.0-1 |
0 |
0.00
|
An R package for the efficient analysis of mutational signatures from cancer genomes |
pekkarr
|
2024-05-03 05:50 (UTC) |
r-repviz
|
1.20.0-1 |
0 |
0.00
|
Replicate oriented Visualization of a genomic region |
BioArchLinuxBot
|
2024-05-02 23:11 (UTC) |
r-repitools
|
1.50.0-1 |
0 |
0.00
|
Epigenomic tools |
BioArchLinuxBot
|
2024-05-03 13:07 (UTC) |
r-regionreport
|
1.38.0-1 |
0 |
0.00
|
Generate HTML or PDF reports for a set of genomic regions or DESeq2/edgeR results |
BioArchLinuxBot
|
2024-05-03 09:23 (UTC) |
r-regionereloaded
|
1.6.0-1 |
0 |
0.00
|
Multiple Association for Genomic Region Sets |
pekkarr
|
2024-05-03 04:29 (UTC) |
r-regioner
|
1.36.0-1 |
0 |
0.00
|
Association analysis of genomic regions based on permutation tests |
BioArchLinuxBot
|
2024-05-03 02:56 (UTC) |
r-recoup
|
1.32.0-1 |
0 |
0.00
|
An R package for the creation of complex genomic profile plots |
BioArchLinuxBot
|
2024-05-08 18:11 (UTC) |
r-rcistarget
|
1.20.0-2 |
0 |
0.00
|
RcisTarget Identify transcription factor binding motifs enriched on a list of genes or genomic regions |
BioArchLinuxBot
|
2024-02-14 18:04 (UTC) |
r-rarevariantvis
|
2.32.0-1 |
0 |
0.00
|
A suite for analysis of rare genomic variants in whole genome sequencing data |
BioArchLinuxBot
|
2024-05-03 05:10 (UTC) |
r-radiogx
|
2.8.0-1 |
0 |
0.00
|
Analysis of Large-Scale Radio-Genomic Data |
BioArchLinuxBot
|
2024-05-03 00:43 (UTC) |
r-r453plus1toolbox
|
1.54.0-1 |
0 |
0.00
|
A package for importing and analyzing data from Roche's Genome Sequencer System |
BioArchLinuxBot
|
2024-05-03 05:01 (UTC) |
r-quantsmooth
|
1.70.0-1 |
0 |
0.00
|
Quantile smoothing and genomic visualization of array data |
BioArchLinuxBot
|
2024-05-01 18:27 (UTC) |
r-qpgraph
|
2.38.0-1 |
0 |
0.00
|
Estimation of genetic and molecular regulatory networks from high-throughput genomics data |
BioArchLinuxBot
|
2024-05-03 12:14 (UTC) |
r-pwrewas
|
1.14.0-2 |
0 |
0.00
|
A user-friendly tool for comprehensive power estimation for epigenome wide association studies (EWAS) |
BioArchLinuxBot
|
2024-02-13 18:12 (UTC) |
r-proteodisco
|
1.10.0-1 |
0 |
0.00
|
Generation of customized protein variant databases from genomic variants, splice-junctions and manual sequences |
BioArchLinuxBot
|
2024-05-03 05:02 (UTC) |
r-profileplyr
|
1.20.0-1 |
0 |
0.00
|
Visualization and annotation of read signal over genomic ranges with profileplyr |
BioArchLinuxBot
|
2024-05-03 05:25 (UTC) |
r-predictionet
|
1.40.0-4 |
0 |
0.00
|
Inference for predictive networks designed for (but not limited to) genomic data |
BioArchLinuxBot
|
2022-06-07 13:19 (UTC) |
r-pogos
|
1.24.0-1 |
0 |
0.00
|
PharmacOGenomics Ontology Support |
BioArchLinuxBot
|
2024-05-03 18:44 (UTC) |
r-plyranges
|
1.24.0-1 |
0 |
0.00
|
A fluent interface for manipulating GenomicRanges |
BioArchLinuxBot
|
2024-05-03 00:53 (UTC) |
r-plyinteractions
|
1.2.0-1 |
0 |
0.00
|
Extending tidy verbs to genomic interactions |
pekkarr
|
2024-05-03 03:35 (UTC) |
r-plsgenomics
|
1.5.3-1 |
0 |
0.00
|
PLS Analyses for Genomics |
BioArchLinuxBot
|
2024-03-28 12:02 (UTC) |
r-plotgardener
|
1.10.0-1 |
0 |
0.00
|
Coordinate-Based Genomic Visualization Package for R |
BioArchLinuxBot
|
2024-05-03 03:31 (UTC) |
r-philr
|
1.30.0-1 |
0 |
0.00
|
Phylogenetic partitioning based ILR transform for metagenomics data |
BioArchLinuxBot
|
2024-05-02 01:08 (UTC) |
r-phenstat
|
2.40.0-1 |
0 |
0.00
|
Statistical analysis of phenotypic data |
BioArchLinuxBot
|
2024-05-01 20:40 (UTC) |
r-phenotest
|
1.52.0-1 |
0 |
0.00
|
Tools to test association between gene expression and phenotype in a way that is efficient, structured, fast and scalable. We also provide tools to do GSEA (Gene set enrichment analysis) and copy number variation. |
BioArchLinuxBot
|
2024-05-03 13:09 (UTC) |
r-phenopath
|
1.28.0-1 |
0 |
0.00
|
Genomic trajectories with heterogeneous genetic and environmental backgrounds |
BioArchLinuxBot
|
2024-05-02 19:44 (UTC) |
r-phenomis
|
1.6.0-1 |
0 |
0.00
|
Postprocessing and univariate analysis of omics data |
pekkarr
|
2024-05-03 00:35 (UTC) |
r-phenogeneranker
|
1.12.0-1 |
0 |
0.00
|
PhenoGeneRanker: A gene and phenotype prioritization tool |
BioArchLinuxBot
|
2024-05-01 23:41 (UTC) |
r-phemd
|
1.18.0-2 |
0 |
0.00
|
Phenotypic EMD for comparison of single-cell samples |
BioArchLinuxBot
|
2024-04-28 18:00 (UTC) |
r-pharmacogx
|
3.8.0-1 |
0 |
0.00
|
Analysis of Large-Scale Pharmacogenomic Data |
BioArchLinuxBot
|
2024-05-03 00:40 (UTC) |
r-pdatk
|
1.12.0-1 |
0 |
0.00
|
Pancreatic Ductal Adenocarcinoma Tool-Kit |
BioArchLinuxBot
|
2024-05-03 00:41 (UTC) |
r-pcan
|
1.32.0-1 |
0 |
0.00
|
Phenotype Consensus ANalysis (PCAN) |
BioArchLinuxBot
|
2024-05-01 19:48 (UTC) |
r-pasilla
|
1.32.0-1 |
0 |
0.00
|
Data package with per-exon and per-gene read counts of RNA-seq samples of Pasilla knock-down by Brooks et al., Genome Research 2011. |
BioArchLinuxBot
|
2024-05-03 13:45 (UTC) |
r-panvizgenerator
|
1.22.0-4 |
0 |
0.00
|
Generate PanViz visualisations from your pangenome |
BioArchLinuxBot
|
2022-07-07 06:06 (UTC) |
r-panr
|
1.50.0-1 |
0 |
0.00
|
Posterior association networks and functional modules inferred from rich phenotypes of gene perturbations |
BioArchLinuxBot
|
2024-05-02 18:32 (UTC) |
r-org.sc.sgd.db
|
3.19.1-1 |
0 |
0.00
|
Genome wide annotation for Yeast |
BioArchLinuxBot
|
2024-05-02 18:46 (UTC) |