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Software

software::software.applied filters:

Quast is Quality Assessment Tool for Genome Assemblies.

Available Versions
Available Versions
Unspecified: 5.0.2 5.2.0

QuickMIRSeq is an integrated pipeline for quick and accurate quantification of known miRNAs and isomiRs by jointly processing multiple samples.

Available Versions
Available Versions
Unspecified: 1.0

CellChat: Inference and analysis of cell-cell communication.

Available Versions
Available Versions
Unspecified: 1.5.0

r-rnaseq is a customerized R module based on <code>R/4.1.1</code> used for RNAseq analysis.

Available Versions
Available Versions
Unspecified: 4.1.1-1 4.1.1-1-rstudio

r-scrnaseq is a customerized R module based on <code>R/4.1.1</code> or <code>R/4.2.0</code> used for scRNAseq analysis.

Available Versions
Available Versions
Unspecified: 4.1.1-1 4.1.1-1-rstudio 4.2.0 4.2.0-rstudio 4.2.3-rstudio

Racon is a consensus module for raw de novo DNA assembly of long uncorrected reads.

Available Versions
Available Versions
Unspecified: 1.4.20 1.5.0

Ragout is a tool for chromosome-level scaffolding using multiple references.

Available Versions
Available Versions
Unspecified: 2.3

Ragtag is a tool for fast reference-guided genome assembly scaffolding.

Available Versions
Available Versions
Unspecified: 2.1.0

The RAPIDS suite of software libraries gives you the freedom to execute end-to-end data science and analytics pipelines entirely on GPUs. It relies on NVIDIA® CUDA® primitives for low-level compute optimization, but exposes that GPU parallelism and high-bandwidth memory speed through user-friendly Python interfaces.

Available Versions
Available Versions
Anvil: 0.12 0.13 0.14 0.15 0.16 0.17 21.06 21.10
Gilbreth: 0.12 0.13 0.14 0.15 0.16 0.17 21.06 21.10
Scholar: 0.12 0.13 0.14 0.15 0.16 0.17 21.06 21.10

RapMap is a testing ground for ideas in quasi-mapping and selective alignment.

Available Versions
Available Versions
Unspecified: 0.6.0

Rasusa: Randomly subsample sequencing reads to a specified coverage.

Available Versions
Available Versions
Unspecified: 0.6.0 0.7.0

Raven-assembler is a de novo genome assembler for long uncorrected reads.

Available Versions
Available Versions
Unspecified: 1.8.1

Raxml (Randomized Axelerated Maximum Likelihood) is a program for the Maximum Likelihood-based inference of large phylogenetic trees.

Available Versions
Available Versions
Unspecified: 8.2.12

Raxml-ng is a phylogenetic tree inference tool which uses maximum-likelihood (ML) optimality criterion.

Available Versions
Available Versions
Unspecified: 1.1.0

Reapr is a tool that evaluates the accuracy of a genome assembly using mapped paired end reads.

Available Versions
Available Versions
Unspecified: 1.0.18

Rebaler is a program for conducting reference-based assemblies using long reads.

Available Versions
Available Versions
Unspecified: 0.2.0

The reciprocal smallest distance (RSD) algorithm accurately infers orthologs between pairs of genomes by considering global sequence alignment and maximum likelihood evolutionary distance between sequences.

Available Versions
Available Versions
Unspecified: 1.1.7

Recycler is a tool designed for extracting circular sequences from de novo assembly graphs.

Available Versions
Available Versions
Unspecified: 0.7

Regtools are tools that integrate DNA-seq and RNA-seq data to help interpret mutations in a regulatory and splicing context.

Available Versions
Available Versions
Unspecified: 1.0.0

RELION for REgularized LIkelihood OptimizatioN implements an empirical Bayesian approach for analysis of electron cryo-microscopy Cryo-EM. Specifically it provides methods of refinement of singular or multiple 3D reconstructions as well as 2D class averages. RELION is an important tool in the study of living cells.

Available Versions
Available Versions
Anvil: 2.1.b1 3.1.0 3.1.2 3.1.3
Gilbreth: 2.1.b1 3.0.8 3.1.0 3.1.2 3.1.3
Scholar: 2.1.b1 3.0.8 3.1.0 3.1.2 3.1.3