10x Library

Literature

Product Literature

Chromium Immune Profiling Solution with Feature Barcoding Technology Product Sheet

Chromium Single Cell Gene Expression Solution with CRISPR Screening Product Sheet

Chromium Single Cell Gene Expression Solution v3 Product Sheet

Chromium Single Cell Gene Expression with Cell Surface Protein Product Sheet

Chromium Genome Sequencing Solution Brochure

Chromium Exome Sequencing Solution Brochure

Chromium de novo Assembly Solution Brochure

Chromium Single Cell Immune Profiling Solution Product Sheet

Chromium Single Cell CNV Solution Product Sheet

Chromium Single Cell ATAC Solution Product Sheet

Chromium Genome Sequencing Solution Product Sheet

Chromium Exome Sequencing Solution Product Sheet

Chromium de novo Assembly Solution Product Sheet

Getting Started with Single Cell Gene Expression

Inside the Chromium Controller

Transcriptional Profiling of 1.3 Million Brain Cells with the Chromium Single Cell 3’ Solution

Single Cell ATAC-Seq for Characterization of Complex Biological Systems

Assessing Tumor Heterogeneity with Single Cell CNV

Pushing the Boundaries of Gene Sensitivity with the Chromium Single Cell Gene Expression v3

Discover Genetic Heterogeneity in Cancer

Characterization of the Tumor Microenvironment

Improving Single Cell Characterization with Simultaneous Gene Expression and Cell Surface Protein Measurements at Scale

Chromium Structural Variant Analysis with Linked-Reads

Chromium Genome Solution and Long Ranger for HLA Analysis

Detection of structural variants using linked-reads with novel algorithms

Characterizing Tumor Heterogeneity at Single Cell Level

Haplotype resolved analysis and improved genome coverage with Linked-Reads

Simultaneous single cell analysis of multiple analytes resolves T cell populations at high resolution

Deciphering the tumor microenvironment cell by cell

Characterizing Genomic Variation and Tumor Heterogeneity in Cancer

A Scalable Microfluidic Platform for Determining Cellular Heterogeneity by Copy Number Detection

Analyzing Infiltrating B Cell Populations in the Tumor Microenvironment Using Single Cell Transcriptomics

Identifying Genetic Variation and Cellular Heterogeneity with a Comprehensive Cancer Analysis Toolkit

Single cell transcriptomics for characterization of normal and diseased endodermal tissues

Dissecting the microenvironment of multiple tumors by transcriptional profiling and immune repertoire sequencing

Single cell transcriptomics for characterization of complex cellular systems

Full spectrum genome analysis with Linked-Read sequencing

How to determine the genome sequence of single insects

Copy Number Profiling of Thousands of Single Cells in Parallel

Assembly of individual chromosomes at megabase scale using 10x Linked-Reads

Resolving the full spectrum of human genetic variation using Linked-Reads

Single cell transcriptomics for characterization of complex systems and biomarker detection

High throughput Linked-Read sequencing for improved small variant calling

Moving into the darkness: Improving variant analysis with Linked-Reads

Linked-Read sequencing for molecular cytogenetics

Long range applications with short read sequencing

Direct determination of genome sequences

Alignment and variant calling in segmental duplications with linked-read data

Single cell mRNA quantification from 1000s of cells in intestinal epithelial cells and bone marrow mononuclear cells using a high-throughput droplet-based system

Enabling more complete genome analysis using 10x Linked-Reads

High-throughput gene expression profiling of complex cell populations using the 10x Chromium Single Cell system

Single cell mRNA quantification from 1000s of cells in intestinal epithelial cells and bone marrow mononuclear cells using a high-throughput droplet-based system

The Linked-Read exome: improved variant calls, inaccessible regions, compound heterozygotes and SV’s from a single library

Deep profiling of thousands of cells from immune systems using scalable single gene expression

Single cell mRNA quantification from 1000s of cells in healthy and malignant tumor samples using a high-throughput droplet-based system

Linked-Reads enable detailed, phased resolution of structural variation in the cancer genome

Enhancing 10x Genomics’ GemCode Technology platform through optimization of QIAGEN’s HMW sample prep solutions

Order your 10x system, today.

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