kallistobustoolskallisto | bustools workflow for pre-processing single-cell RNA-seq data
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velodynDynamical systems methods for RNA velocity analysis
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kanaSingle cell analysis in the browser
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scCATCHAutomatic Annotation on Cell Types of Clusters from Single-Cell RNA Sequencing Data
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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.
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cellSNPPileup biallelic SNPs from single-cell and bulk RNA-seq data
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NGSNext-Gen Sequencing tools from the Horvath Lab
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SCopeLoomRR package (compatible with SCope) to create generic .loom files and extend them with other data e.g.: SCENIC regulons, Seurat clusters and markers, ...
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pychopperA tool to identify, orient, trim and rescue full length cDNA reads
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dee2Digital Expression Explorer 2 (DEE2): a repository of uniformly processed RNA-seq data
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GLUEGraph-linked unified embedding for single-cell multi-omics data integration
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ssGSEA2.0Single sample Gene Set Enrichment analysis (ssGSEA) and PTM Enrichment Analysis (PTM-SEA)
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sintoTools for single-cell data processing
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DEGreportCreate a cromphensive report of DEG list coming from any analysis of RNAseq data
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RATTLEReference-free reconstruction and error correction of transcriptomes from Nanopore long-read sequencing
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PandoMultiome GRN inference.
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dropPipeline to find aberrant events in RNA-Seq data, useful for diagnosis of rare disorders
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anndata2riConvert between AnnData and SingleCellExperiment
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scMCAMouse cell atlas
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DGCADifferential Gene Correlation Analysis
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biojupiesAutomated generation of tailored bioinformatics Jupyter Notebooks via a user interface.
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rnatoyA proof of concept RNA-Seq pipeline with Nextflow
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READemptionA pipeline for the computational evaluation of RNA-Seq data
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SCOPE-toolsSingle-Cell Omics Preparation Entity Tools
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TCC-GUI📊 Graphical User Interface for TCC package
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cellsnp-liteEfficient genotyping bi-allelic SNPs on single cells
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snakefiles🐍 Snakefiles for common RNA-seq data analysis workflows.
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cnaCovarying neighborhood analysis (CNA) is a method for finding structure in- and conducting association analysis with multi-sample single-cell datasets.
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arribaFast and accurate gene fusion detection from RNA-Seq data
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NGI-RNAseqNextflow RNA-Seq Best Practice analysis pipeline, used at the SciLifeLab National Genomics Infrastructure.
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GREINGREIN : GEO RNA-seq Experiments Interactive Navigator
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NebulosaR package to visualize gene expression data based on weighted kernel density estimation
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trVAEConditional out-of-distribution prediction
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scadenDeep Learning based cell composition analysis with Scaden.
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PECAPECA is a software for inferring context specific gene regulatory network from paired gene expression and chromatin accessibility data
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