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johandahlberg/awesome-10x-genomics

List of tools and resources related to the 10x Genomics GEMCode/Chromium system

Awesome 10x Genomics

10x genomics logo

This repository attempts to gather tools related to the GEMCode/Chromium platforms from 10x Genomics.

How to contribute

Contribute to this repo by creating a PR with one or more new tools, and a link(s) to the corresponding repo(s) and a short description of what the tool does.

Linked reads

  • arcs -
    Scaffold genome sequence assemblies using linked read data

  • Athena -
    Read cloud assembler for metagenomes

  • BarCrawler -
    An easy to use QC package for 10X genomics barcoded reads.

  • bxtools -
    Tools for analyzing 10x data

  • EMerAld -
    Fast and accurate alignment of barcoded short-reads

  • grocsvs -
    Genome-wide reconstruction of complex structural variants

  • LRSIM -
    A simulator for linked reads

  • NAIBR -
    Identifies novel adjacencies created by structural variation events such as deletions, duplications, inversions, and complex rearrangements

  • Samovar -
    Somatic (mosaic) SNV caller for 10X Genomics data using random forest classification and feature-based filters

  • tenx_utils -
    Utility functions for 10x data

  • Tigmint -
    Correct misassemblies using Linked Reads

  • Topsorter -
    Graphic assement of structural variants

  • scaff10x -
    Scaffolding assemblies using linked read data

  • SuperNova -
    10x Genomics Linked-Read Diploid De Novo Assembler

  • SVenX -
    Pipeline for SV detection using 10X genomics data

Single cell

  • monocle-release -
    R analysis toolkit for single cell genomics

  • seurat -
    R toolkit for single cell genomics

  • Scanpy -
    Toolkit for simulating and analyzing single cell data

  • TENxGenomics -
    R interface to the 1.3 M single cell data set from 10x Genomics

  • 10xQC -
    Database of 10x single cell QC metrics submitted by research groups worldwide

  • VarTrix -
    Single-Cell Genotyping tool

Spatial transcriptomics

  • FlashDeconv -
    High-performance spatial transcriptomics deconvolution for Visium HD and other 10x platforms. Processes 1M spots in ~3 minutes.

  • Squidpy -
    Spatial single cell analysis in Python, builds on scanpy and anndata

  • cell2location -
    Bayesian model for mapping fine-grained cell types in spatial transcriptomics

Contributors

Other
Created June 20, 2017
Updated February 23, 2026
johandahlberg/awesome-10x-genomics | GitHunt