cardelinoClone identification from single-cell data
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DellXPS15-9550-OSXTutorial for a full working Mac OS (10.11 up to 11.0) enviroment on the Dell XPS 15 (9550)
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purge-nvdaOptimize external graphics for macs with discrete NVIDIA GPUs.
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x16-xcieXtremely Compact Interpreter - An adventure game engine for the Commander X16
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smartas📓Notebook of Climente-González et al. (2017), The Functional Impact of Alternative Splicing in Cancer.
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psichomicsInteractive R package to quantify, analyse and visualise alternative splicing
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Whippet.jlLightweight and Fast; RNA-seq quantification at the event-level
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dropEstPipeline for initial analysis of droplet-based single-cell RNA-seq data
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fastq utilsValidation and manipulation of FASTQ files, scRNA-seq barcode pre-processing and UMI quantification.
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babelDeep learning model for single-cell inference of multi-omic profiles from a single input modality.
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scarchesReference mapping for single-cell genomics
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cellrouterReconstruction of complex single-cell trajectories using CellRouter
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souporcellClustering scRNAseq by genotypes
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zellkonverterConversion between scRNA-seq objects
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HarmonyHarmony framework for connecting scRNA-seq data from discrete time points
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scHPFSingle-cell Hierarchical Poisson Factorization
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cTPnetcTPnet Package
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celltypistA tool for semi-automatic cell type annotation
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BEERBEER: Batch EffEct Remover for single-cell data
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scarfToolkit for highly memory efficient analysis of single-cell RNA-Seq, scATAC-Seq and CITE-Seq data. Analyze atlas scale datasets with millions of cells on laptop.
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SHARPSHARP: Single-cell RNA-seq Hyper-fast and Accurate processing via ensemble Random Projection
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symphonyEfficient and precise single-cell reference atlas mapping with Symphony
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vireoDemultiplexing pooled scRNA-seq data with or without genotype reference
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TangramSpatial alignment of single cell transcriptomic data.
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northstarSingle cell type annotation guided by cell atlases, with freedom to be queer
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scGEAToolboxscGEAToolbox: Matlab toolbox for single-cell gene expression analyses
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cerebraA tool for fast and accurate summarizing of variant calling format (VCF) files
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scAlignA deep learning-based tool for alignment and integration of single cell genomic data across multiple datasets, species, conditions, batches
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ALRAImputation method for scRNA-seq based on low-rank approximation
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