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Instead, please submit your tool to the [scverse ecosystem package listing](https://scverse.org/packages/#ecosystem).
Interactive manifold viewers.
- cellxgene via direct reading of
.h5ad{small}CZI - cirrocumulus via direct reading of
.h5ad{small}Broad Inst. - cell browser via exporing through {func}
~scanpy.external.exporting.cellbrowser{small}UCSC - SPRING via exporting through {func}
~scanpy.external.exporting.spring_project{small}Harvard Med - vitessce for purely browser based viewing of zarr formatted AnnData files {smaller}
Harvard Med
- the Gene Expression Analysis Resource {small}
U Maryland - the Galaxy Project for the Human Cell Atlas [tweet] {small}
U Freiburg - the Expression Atlas {small}
EMBL-EBI
- scVelo {small}
Helmholtz Munich
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squidpy {small}
Helmholtz MunichSquidpy is a comprehensive toolkit for working with spatial single cell omics data.
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PASTE {small}
PrincetonPASTE is a computational method to align and integrate spatial transcriptomics data across adjacent tissue slices by leveraging both gene expression similarity and spatial distances between spots.
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bento 🍱 {small}
UC San DiegoBento is an accessible Python toolkit for performing subcellular analysis of spatial transcriptomics data.
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MUON and MuData {small}
EMBL/ DKFZMUON, and it's associated data structure MuData are designed to organise, analyse, visualise, and exchange multimodal data. MUON enables a range of analyses for ATAC and CITE-seq, from data preprocessing to flexible multi-omics alignment.
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scirpy {small}
Medical University of Innsbruckscirpy is a scanpy extension to expore single-cell T-cell receptor (TCR) and B-cell receptor (BCR) repertoires.
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dandelion {small}
University of Cambridgedandelion is a single-cell BCR-seq network analysis package that integrates with transcriptomic data analyzed via scanpy.
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Swan {small}
UC IrvineSwan is a Python library designed for the analysis and visualization of transcriptomes, especially with long-read transcriptomes in mind. Users can add transcriptomes from different datasets and explore distinct splicing and expression patterns across datasets.
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scvi-tools {small}
Berkeleyscvi-tools hosts deep generative models (DGM) for end-to-end analysis of single-cell omics data (e.g., scVI, scANVI, totalVI). It also contains several primitives to build novel DGMs.
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CellRank {small}
Helmholtz MunichCellRank is a framework to uncover cellular dynamics based on single-cell data. It incorporates modalities such as RNA velocity, pseudotime, developmental potential, real-time information, etc.
- diffxpy {small}
Helmholtz Munich
(eco-data-integration)=
- scanaroma {small}
MIT
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triku 🦔 {small}
Biodonostia Health Research Institute -
CIARA {small}
Helmholtz MunichCIARA is an algorithm for feature selection, that aims for the identification of rare cell types via scRNA-Seq data in scanpy.
Analyses using curated prior knowledge
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decoupler is a collection of footprint enrichment methods that allows to infer transcription factor or pathway activities. {small}
Institute for Computational Biomedicine, Heidelberg University -
Cubé {small}
Harvard UniversityIntuitive Nonparametric Gene Network Search Algorithm that learns from existing biological pathways & multiplicative gene interference patterns.