Linked-Reads Genomics

Linked-Reads leverages microfluidics to partition and barcode HMW DNA to generate a data type that provides contextual information of the genome from short-reads. Our technology allows you to consolidate multiple assays into a single, powerful workflow with low input requirements.

Discontinuation of Linked-Reads

At 10x Genomics, we are committed to enabling your research and providing you with the best experience to make scientific discoveries. Earlier this year, as a part of our product life cycle management, we notified you about refinements to some of our on-market product offerings.

As of June 30, 2020, we discontinued the sale of our Chromium Genome and Exome product lines. We will not be releasing new versions of these products.

We thank you for your partnership and are committed to providing the highest-quality technical and software support.

Please contact your Sales Executive, Field Application Scientist, or email our Support Team at support@10xgenomics.com with any questions.

What are Linked-Reads?

Linked-Reads, a sequencing technology developed by 10x Genomics, leverages microfluidics to partition and barcode HMW DNA to generate a data type that provides contextual information of the genome from short-reads. Our technology allows you to consolidate multiple assays into a single, powerful workflow with low input requirements. Simply put, Linked-Reads provide long-range information from short-read sequencing data, so you can find the information you may not even realize you’ve been missing.

Linked-Reads Resources