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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 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 & Next GEM 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

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