Genome Sequencing

About Linked Reads for Genome Sequencing

The Chromium Genome Sequencing Solution provides Long read information from short reads.

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.

Benefits

  • Long-range information from a short-read BGI® and 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

Workflow

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For more information including; Software, Application Notes, Publications and more click here