getting-started-with-genomics-tools-and-resources VS scanpy

Compare getting-started-with-genomics-tools-and-resources vs scanpy and see what are their differences.

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getting-started-with-genomics-tools-and-resources scanpy
2 5
1,101 1,763
- 1.7%
4.8 9.3
24 days ago 1 day ago
Shell Python
- BSD 3-clause "New" or "Revised" License
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.

getting-started-with-genomics-tools-and-resources

Posts with mentions or reviews of getting-started-with-genomics-tools-and-resources. We have used some of these posts to build our list of alternatives and similar projects.

scanpy

Posts with mentions or reviews of scanpy. We have used some of these posts to build our list of alternatives and similar projects. The last one was on 2022-05-23.

What are some alternatives?

When comparing getting-started-with-genomics-tools-and-resources and scanpy you can also consider the following projects:

manjaro-linux - Shell scripts for setting up Manjaro Linux for Python programming and deep learning

scikit-learn - scikit-learn: machine learning in Python

bioconda-recipes - Conda recipes for the bioconda channel.

dash - Data Apps & Dashboards for Python. No JavaScript Required.

biowasm - WebAssembly modules for genomics

data-science-ipython-notebooks - Data science Python notebooks: Deep learning (TensorFlow, Theano, Caffe, Keras), scikit-learn, Kaggle, big data (Spark, Hadoop MapReduce, HDFS), matplotlib, pandas, NumPy, SciPy, Python essentials, AWS, and various command lines.

TeamTeri - Bioinformatics on GCP, AWS or Azure

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

metaflow-on-kubernetes-docs - Documentation For Running Metaflow on Kubernetes

dash-cytoscape - Interactive network visualization in Python and Dash, powered by Cytoscape.js

pagoda2 - R package for analyzing and interactively exploring large-scale single-cell RNA-seq datasets