hgvs VS mixcr

Compare hgvs vs mixcr and see what are their differences.

hgvs

Python library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs` (by biocommons)

mixcr

MiXCR is an ultimate software platform for analysis of Next-Generation Sequencing (NGS) data for immune profiling. (by milaboratory)
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hgvs mixcr
1 1
231 310
1.3% 2.6%
8.3 9.7
7 days ago 3 days ago
Python Kotlin
Apache License 2.0 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.

hgvs

Posts with mentions or reviews of hgvs. We have used some of these posts to build our list of alternatives and similar projects.

mixcr

Posts with mentions or reviews of mixcr. We have used some of these posts to build our list of alternatives and similar projects.

What are some alternatives?

When comparing hgvs and mixcr you can also consider the following projects:

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

salmon - 🐟 🍣 🍱 Highly-accurate & wicked fast transcript-level quantification from RNA-seq reads using selective alignment

ariba - Antimicrobial Resistance Identification By Assembly

galaxy - Data intensive science for everyone.

rnaseq - RNA-seq analyses.

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

alevin-fry - 🐟 🔬🦀 alevin-fry is an efficient and flexible tool for processing single-cell sequencing data, currently focused on single-cell transcriptomics and feature barcoding.

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