Discover What You Have Been Missing

Contact Me Request a Quote

The Chromium Genome Sequencing Solution

Discover What You Have Been Missing

The Chromium Genome uses the power of Linked-Reads to fully resolve genic phasing, reveal structural
variation and detect variants in previously inaccessible and complex regions of the genome.

Our Solution Features

  • Long-range information from a short-read Illumina® sequencer
  • High-quality libraries from as little as 1 ng of genomic DNA
  • Turn-key analysis pipeline and visualization tools
  • Call and phase major classes of structural variants (SVs) like deletions, inversions, and translocations, even in genes inaccessible to short-read sequencers
  • Phase SNVs, indels and SVs across >10 Mb haplotype blocks
View the Workflow
Genome Solution Suite

Watch: How It Works

Long-Range Information from Short-Read Sequencing Data

See the workflow for whole exome and genome sequencing and how our technology partitions and barcodes DNA. Understand how the Linked-Reads enable long-range analysis and phasing of SNVs, indels, and structural variants.

The Chromium Controller

Compact, Sleek, Efficient.

The compact, sleek Chromium Controller rapidly and efficiently combines large partition numbers with a massively diverse barcode library to generate >100,000 barcode-containing partitions in a matter of minutes. The Chromium Controller fits on a standard laboratory bench and allows a user to run any Chromium Solution, from genome to single cell analysis.

View Our Controller Gallery
Genome Controller

Product List

Chromium Genome Sequencing Solution

Reagents & Consumables

Reactions
Product Code
Chromium Genome Chip Kit v2
48 rxns
120257
Chromium Genome HT Library & Gel Bead Kit v2
96 rxns
120261
Chromium Genome Library Kit & Gel Bead Kit v2
16 rxns
120258
Chromium i7 Multiplex Kit
96 rxns
120262

Instruments & Accessories

Warranty
Product Code
Chromium Controller & Accessory Kit
120223
120246

Accessories

Warranty
Product Code
Chromium Automation Accessory Kit
1000008

Software

Long Ranger Analysis Pipelines
Loupe Genome Browser
Scientific Seminars

Dissecting Complex Systems with Multidimensional Data

 
  • Sarah Garcia
10x Genomics, Inc.
March 21, 2019

Automation Compatible Linked-Read Analysis of Dried Blood Spots

 
  • Madhuri Hegde, Ph.D.
PerkinElmer
December 07, 2017
ASHG 2017 Orlando, FL

Population Scale Genome Study of the Faroese Population Using Linked-Reads

 
  • Noomi Oddmarsdóttir Gregersen
FarGen Project
November 01, 2017
Nature Webinar

Genome-wide Reconstruction of Complex Structural Variants

 
  • Noah Spies
Stanford University
March 21, 2017
User Group Meeting – San Francisco, CA

Universal Approach for Noninvasive Prenatal Testing of Single Gene Diseases

 
  • Winnie Hui
The Chinese University of Hong Kong
February 13, 2017
AGBT Annual Meeting – Hollywood, FL

Order your Chromium Controller, today.

Request a Quote

Order your 10x system, today.