galaxy VS ariba

Compare galaxy vs ariba and see what are their differences.

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galaxy ariba
4 1
1,319 154
1.7% 1.9%
10.0 3.0
3 days ago 7 months ago
Python Python
GNU General Public License v3.0 or later GNU General Public License v3.0 or later
The number of mentions indicates the total number of mentions that we've tracked plus the number of user suggested alternatives.
Stars - the number of stars that a project has on GitHub. Growth - month over month growth in stars.
Activity is a relative number indicating how actively a project is being developed. Recent commits have higher weight than older ones.
For example, an activity of 9.0 indicates that a project is amongst the top 10% of the most actively developed projects that we are tracking.

galaxy

Posts with mentions or reviews of galaxy. We have used some of these posts to build our list of alternatives and similar projects. The last one was on 2023-06-17.

ariba

Posts with mentions or reviews of ariba. We have used some of these posts to build our list of alternatives and similar projects. The last one was on 2023-03-25.

What are some alternatives?

When comparing galaxy and ariba you can also consider the following projects:

nextflow - A DSL for data-driven computational pipelines

abricate - :mag_right: :pill: Mass screening of contigs for antimicrobial and virulence genes

Biopython - Official git repository for Biopython (originally converted from CVS)

MGEfinder - A toolbox for identifying mobile genetic element (MGE) insertions from short-read sequencing data of bacterial isolates.

deepvariant - DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.

abritamr - A pipeline for running AMRfinderPlus and collating results into functional classes

fastp - An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)

edgecase - A framework for extracting telomeric reads from single-molecule sequencing experiments, describing their sequence variation and motifs, and for haplotype inference.

sarek - Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing

16SMaRT - 16s rRNA Sequencing Meta-analysis Reproducibility Tool (using mothur).

galaxy_ng - Ansible Galaxy Server - Issues on https://forum.ansible.com Docs on https://galaxy-ng.readthedocs.io/

hgvs - Python library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`