Exome Sequencing

Reach Beyond the Standard Exome

Chromium Exome Sequencing Solution

Reach Beyond the Standard Exome

The Chromium Exome provides long range information, enabling phasing, structural variant detection,
and copy number determination. Low complexity and repetitive regions previously missed
with short-read sequencing are now accessible.

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Our Solution Features

High-quality libraries from only 1 ng of genomic DNA
Detect large scale structural variants (SVs) including gene fusions
Call and phase variants across the entire exome
Detect variants in genes inaccessible to standard short-read libraries
Useful for high sequence homology, including problematic duplications, inversions and pseudogenes
Optimized baits utilize Linked-Reads for intron-spanning

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.

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.

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Product List

Chromium Exome Sequencing Solution

Available for use only with the Chromium Controller instrument Part Number 120223 and 120246, or the Chromium Single Cell Controller instrument Part Number 120263 and 120212.