random123
|
1.14.0-1 |
0 |
0.00
|
counter-based random number generators library |
kleintux
|
2022-01-12 08:12 (UTC) |
random-rs
|
0.2.4-1 |
0 |
0.00
|
Generate random numbers from CLI |
onedwide
|
2023-11-28 20:45 (UTC) |
random
|
1.3-1 |
1 |
0.01
|
Random number generator. |
ivanch
|
2020-01-10 14:08 (UTC) |
rand
|
1.0.4-1 |
0 |
0.00
|
A simple program to write random numbers/characters to standard output |
Nurmukhametov
|
2021-11-07 10:13 (UTC) |
r-twoddpcr
|
1.26.0-1 |
0 |
0.00
|
Classify 2-d Droplet Digital PCR (ddPCR) data and quantify the number of starting molecules |
BioArchLinuxBot
|
2023-10-25 22:37 (UTC) |
r-titancna
|
1.40.0-1 |
0 |
0.00
|
Subclonal copy number and LOH prediction from whole genome sequencing of tumours |
BioArchLinuxBot
|
2023-10-27 12:41 (UTC) |
r-suitor
|
1.4.0-3 |
0 |
0.00
|
Selecting the number of mutational signatures through cross-validation |
pekkarr
|
2024-04-25 12:26 (UTC) |
r-smap
|
1.66.0-2 |
0 |
0.00
|
A Segmental Maximum A Posteriori Approach to Array-CGH Copy Number Profiling |
BioArchLinuxBot
|
2024-04-05 18:07 (UTC) |
r-sitmo
|
2.0.2-4 |
0 |
0.00
|
Parallel Pseudo Random Number Generator (PPRNG) 'sitmo' Header Files |
BioArchLinuxBot
|
2022-06-06 15:17 (UTC) |
r-setrng
|
2024.2.1-1 |
0 |
0.00
|
Set (Normal) Random Number Generator and Seed |
BioArchLinuxBot
|
2024-02-18 18:02 (UTC) |
r-seqcna.annot
|
1.38.0-2 |
0 |
0.00
|
Annotation for the copy number analysis of deep sequencing cancer data with seqCNA |
BioArchLinuxBot
|
2024-03-15 14:10 (UTC) |
r-seqcna
|
1.48.0-1 |
0 |
0.00
|
Copy number analysis of high-throughput sequencing cancer data |
BioArchLinuxBot
|
2023-10-25 22:08 (UTC) |
r-selectksigs
|
1.14.0-1 |
0 |
0.00
|
Selecting the number of mutational signatures using a perplexity-based measure and cross-validation |
BioArchLinuxBot
|
2023-10-27 13:13 (UTC) |
r-scope
|
1.14.0-1 |
0 |
0.00
|
A normalization and copy number estimation method for single-cell DNA sequencing |
BioArchLinuxBot
|
2023-10-27 11:31 (UTC) |
r-rngwell
|
0.10.9-3 |
0 |
0.00
|
Toolbox for WELL Random Number Generators |
BioArchLinuxBot
|
2024-03-15 14:18 (UTC) |
r-rngtools
|
1.5.2-4 |
0 |
0.00
|
Utility Functions for Working with Random Number Generators |
BioArchLinuxBot
|
2022-06-06 13:15 (UTC) |
r-rhpcblasctl
|
0.23.42-4 |
0 |
0.00
|
Control the Number of Threads on 'BLAS' |
BioArchLinuxBot
|
2024-04-24 19:17 (UTC) |
r-rebus.numbers
|
0.0.1-7 |
0 |
0.00
|
Numeric Extensions for the 'rebus' Package |
BioArchLinuxBot
|
2024-04-14 12:11 (UTC) |
r-rbeta2009
|
1.0-3 |
0 |
0.00
|
The Beta Random Number and Dirichlet Random Vector Generating Functions |
pekkarr
|
2024-04-24 22:42 (UTC) |
r-randtoolbox
|
2.0.4-3 |
0 |
0.00
|
Toolbox for Pseudo and Quasi Random Number Generation and Random Generator Tests |
BioArchLinuxBot
|
2024-04-14 12:15 (UTC) |
r-purecn
|
2.8.1-1 |
0 |
0.00
|
Copy number calling and SNV classification using targeted short read sequencing |
BioArchLinuxBot
|
2023-11-23 00:11 (UTC) |
r-pscbs
|
0.67.0-1 |
0 |
0.00
|
Analysis of Parent-Specific DNA Copy Numbers |
BioArchLinuxBot
|
2024-02-18 00:02 (UTC) |
r-phenotest
|
1.50.0-1 |
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
|
2023-10-26 06:45 (UTC) |
r-numbers
|
0.8.5-3 |
1 |
0.00
|
Number-Theoretic Functions |
BioArchLinuxBot
|
2024-02-09 20:08 (UTC) |
r-nbclust
|
3.0.1-6 |
0 |
0.00
|
Determining the Best Number of Clusters in a Data Set |
BioArchLinuxBot
|
2024-03-12 18:06 (UTC) |
r-mmand
|
1.6.3-3 |
0 |
0.00
|
Mathematical Morphology in Any Number of Dimensions |
pekkarr
|
2024-04-25 09:06 (UTC) |
r-mbpcr
|
1.56.0-1 |
0 |
0.00
|
Bayesian Piecewise Constant Regression for DNA copy number estimation |
BioArchLinuxBot
|
2023-10-27 08:48 (UTC) |
r-inpower
|
1.38.0-2 |
0 |
0.00
|
An R package for computing the number of susceptibility SNPs |
BioArchLinuxBot
|
2024-04-07 18:04 (UTC) |
r-infercnv
|
1.18.1-1 |
0 |
0.00
|
Infer Copy Number Variation from Single-Cell RNA-Seq Data |
BioArchLinuxBot
|
2023-12-03 00:15 (UTC) |
r-igc
|
1.32.0-1 |
0 |
0.00
|
An integrated analysis package of Gene expression and Copy number alteration |
BioArchLinuxBot
|
2023-10-25 20:07 (UTC) |
r-icnv
|
1.22.0-1 |
0 |
0.00
|
Integrated Copy Number Variation detection |
BioArchLinuxBot
|
2023-10-27 13:12 (UTC) |
r-ic10
|
1.5-7 |
0 |
0.00
|
A Copy Number and Expression-Based Classifier for Breast Tumours |
BioArchLinuxBot
|
2024-04-14 12:06 (UTC) |
r-howmany
|
0.3.1-8 |
0 |
0.00
|
A lower bound for the number of correct rejections |
BioArchLinuxBot
|
2024-04-15 18:01 (UTC) |
r-hmmcopy
|
1.44.0-2 |
0 |
0.00
|
Copy number prediction with correction for GC and mappability bias for HTS data |
BioArchLinuxBot
|
2024-04-06 18:06 (UTC) |
r-gridextra
|
2.3-1 |
1 |
0.00
|
Provides a number of user-level functions to work with "grid" graphics, notably to arrange multiple grid-based plots on a page, and draw tables. |
portaloffreedom
|
2018-06-11 10:17 (UTC) |
r-genocn
|
1.54.0-2 |
0 |
0.00
|
genotyping and copy number study tools |
BioArchLinuxBot
|
2024-03-29 12:05 (UTC) |
r-genelendatabase
|
1.38.0-1 |
0 |
0.00
|
Lengths of mRNA transcripts for a number of genomes |
BioArchLinuxBot
|
2023-10-27 10:23 (UTC) |
r-frenchfish
|
1.14.0-1 |
0 |
0.00
|
Poisson Models for Quantifying DNA Copy-number from FISH Images of Tissue Sections |
BioArchLinuxBot
|
2023-10-25 21:05 (UTC) |
r-exomecopy
|
1.48.0-1 |
0 |
0.00
|
Copy number variant detection from exome sequencing read depth |
BioArchLinuxBot
|
2023-10-26 03:16 (UTC) |
r-dqrng
|
0.3.2-2 |
0 |
0.00
|
Fast Pseudo Random Number Generators |
BioArchLinuxBot
|
2024-01-21 18:01 (UTC) |
r-dnacopy
|
1.76.0-3 |
0 |
0.00
|
DNA Copy Number Data Analysis |
BioArchLinuxBot
|
2024-04-24 18:52 (UTC) |
r-crlmm
|
1.60.0-1 |
0 |
0.00
|
Genotype Calling (CRLMM) and Copy Number Analysis tool for Affymetrix SNP 5.0 and 6.0 and Illumina arrays |
BioArchLinuxBot
|
2023-10-27 08:48 (UTC) |
r-copynumberplots
|
1.18.0-1 |
0 |
0.00
|
Create Copy-Number Plots using karyoploteR functionality |
BioArchLinuxBot
|
2023-10-27 15:32 (UTC) |
r-copynumber
|
1.38.0-3 |
0 |
0.00
|
Segmentation of single- and multi-track copy number data by penalized least squares regression. |
BioArchLinuxBot
|
2023-11-05 18:02 (UTC) |
r-conumee
|
1.36.0-1 |
0 |
0.00
|
Enhanced copy-number variation analysis using Illumina DNA methylation arrays |
BioArchLinuxBot
|
2023-10-27 13:37 (UTC) |
r-codex
|
1.34.0-1 |
0 |
0.00
|
A Normalization and Copy Number Variation Detection Method for Whole Exome Sequencing |
BioArchLinuxBot
|
2023-10-27 11:32 (UTC) |
r-cnvrd2
|
1.40.0-1 |
0 |
0.00
|
CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data. |
BioArchLinuxBot
|
2023-10-27 12:54 (UTC) |
r-cnvmetrics
|
1.6.0-3 |
0 |
0.00
|
Copy Number Variant Metrics |
pekkarr
|
2024-04-26 13:45 (UTC) |
r-cnviz
|
1.10.0-1 |
0 |
0.00
|
Copy Number Visualization |
BioArchLinuxBot
|
2023-10-27 15:51 (UTC) |
r-cnvgsa
|
1.46.0-1 |
0 |
0.00
|
Gene Set Analysis of (Rare) Copy Number Variants |
BioArchLinuxBot
|
2023-10-26 02:17 (UTC) |