|
perl-test-script
|
public |
Basic cross-platform tests for scripts
|
2025-04-22 |
|
plantcv
|
public |
An image processing package for plant phenotyping.
|
2025-04-22 |
|
perl-probe-perl
|
public |
Information about the currently running perl
|
2025-04-22 |
|
cgat-apps
|
public |
Computational Genomics Analysis Toolkit.
|
2025-04-22 |
|
ivar
|
public |
iVar is a computational package that contains functions broadly useful for viral amplicon-based sequencing.
|
2025-04-22 |
|
sbg-cwl-runner
|
public |
A CWL Runner for SBG platform
|
2025-04-22 |
|
refinem
|
public |
A toolbox for improving population genomes.
|
2025-04-22 |
|
epa-ng
|
public |
Massively parallel phylogenetic placement of genetic sequences
|
2025-04-22 |
|
nullarbor
|
public |
Reads to report pipeline for bacterial isolate NGS data
|
2025-04-22 |
|
r-rrbgen
|
public |
A lightweight limited functionality R bgen read/write library
|
2025-04-22 |
|
sample-sheet
|
public |
An Illumina Sample Sheet parsing library
|
2025-04-22 |
|
seqlogo
|
public |
Python port of the R Bioconductor `seqlogo` package
|
2025-04-22 |
|
nemo
|
public |
Individual-based forward-time genetics simulation software
|
2025-04-22 |
|
goslimmer
|
public |
GOSlimmer transforms GO annotations to a slimmed version of GO
|
2025-04-22 |
|
goenrichment
|
public |
GOEnrichment analyses a set of gene products for GO term enrichment
|
2025-04-22 |
|
perl-text-template-simple
|
public |
Simple text template engine
|
2025-04-22 |
|
matlock
|
public |
Simple tools for working with Hi-C data
|
2025-04-22 |
|
scaffold_builder
|
public |
Scaffold_builder: Combining de novo and reference-guided assembly with Scaffold_builder.
|
2025-04-22 |
|
perl-bio-rna-rnaalisplit
|
public |
Split and deconvolute structural RNA multiple sequence alignments
|
2025-04-22 |
|
perl-array-set
|
public |
Perform set operations on arrays
|
2025-04-22 |
|
enabrowsertools
|
public |
enaBrowserTools is a set of scripts that interface with the ENA web services to download data from ENA easily
|
2025-04-22 |
|
anise_basil
|
public |
BASIL is a method to detect breakpoints for structural variants (including insertion breakpoints) from aligned paired HTS reads in BAM format. ANISE is a method for the assembly of large insertions from paired reads in BAM format and a list candidate insert breakpoints as generated by BASIL.
|
2025-04-22 |
|
bcool
|
public |
BCOOL is a read corrector for NGS sequencing data that align reads on a de Bruijn graph. Version described at (https://arxiv.org/abs/1711.03336) presented at RECOMB-seq 2018
|
2025-04-22 |
|
fastsimbac
|
public |
Models bacterial recombination
|
2025-04-22 |
|
cromshell
|
public |
Command-line interface to the Cromwell workflow manager
|
2025-04-22 |
