Scripts developed to work with 10x Genomics sequencing results

Pipeline for SV detection using 10X genomics data

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

Non-official Git repository for R package cellrangerRkit (currently not available elsewhere; I'm not affiliated with 10x)

adtseq provides simple Rcpp methods to identify Antibody-Derived-Tags in single cell CITE/REAP-seq data

Paper list of single cell omics

Preliminary study to figure out how many larval gonads are needed for RNA-Seq

De novo assembly pipeline for 10X linked-reads using Supernova

R package: {rfca} Random forest-based cell annotation methods for scRNAseq analysis. {rfca} contains methods which identifies cell types using machine learning trained on a diversity of cell types, without the need for a labelled training dataset. It also allows you to train your own cell prediction models with your own labels (cell type, subtyp…

Analysis of subclonal copy number alterations (CNA) and loss of heterozygosity (LOH) in cancer

R script built on Seurat objects to analyze 10X single-cell expression data

CWL toolkit for single-cell sequencing data analysis

Standalone tool and library allowing to work with barcoded linked-reads

Sanger Cellular Genetics single-cell ATAC-seq pipeline.

Single-cell preprocessing pipelines, such as converting raw bcl files, make fastqs and then generating quantified matrix, etc

Download fastqs or supplementary files from GEO and upload to hca-util bucket

Collection of tools and resources for linked-reads

simplified cellranger for long-read data

Cloupe reader

Convert your STDeconvolve-generated and EnrichR-decoded topics into Seurat spatial clustering information via AUCell