This repository attempts to gather tools related to the GEMCode/Chromium platforms from 10x Genomics.
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.
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arcs - Scaffold genome sequence assemblies using linked read data
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Athena - Read cloud assembler for metagenomes
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BarCrawler - An easy to use QC package for 10X genomics barcoded reads.
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bxtools - Tools for analyzing 10x data
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EMerAld - Fast and accurate alignment of barcoded short-reads
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grocsvs - Genome-wide reconstruction of complex structural variants
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LRSIM - A simulator for linked reads
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NAIBR - Identifies novel adjacencies created by structural variation events such as deletions, duplications, inversions, and complex rearrangements
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tenx_utils - Utility functions for 10x data
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Tigmint - Correct misassemblies using Linked Reads
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Topsorter - Graphic assement of structural variants
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scaff10x - Scaffolding assemblies using linked read data
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SuperNova - 10x Genomics Linked-Read Diploid De Novo Assembler
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SVenX - Pipeline for SV detection using 10X genomics data
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monocle-release - R analysis toolkit for single cell genomics
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seurat - R toolkit for single cell genomics
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Scanpy - Toolkit for simulating and analyzing single cell data
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TENxGenomics - R interface to the 1.3 M single cell data set from 10x Genomics
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10xQC - Database of 10x single cell QC metrics submitted by research groups worldwide
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VarTrix - Single-Cell Genotyping tool