Explore the portal

Explore the portal

Bioinformatic insights, faster.

  1. Prepare libraries with Dovetail Linked-read kit

  2. Purchase portal credits

  3. Sequence on your standard short read platform

  4. Submit your FASTQ files into the portal

  5. Explore your interactive report

Launch Portal

Dovetail Analysis Portal Overview for Somatic Variant Detection

Covers uploading data, running analysis, and exploring insights.

Purchase Portal Credits

Dovetail Analysis Portal Credit Dovetail Analysis Portal Credit
Dovetail Analysis Portal Credit
$140.00

The Dovetail Analysis Portal is available to all Dovetail Genomics customers and enables the streamlined analysis of NGS FASTQ files generated from Dovetail linked-read libraries. The portal accepts standard paired-end sequences in fastq format and outputs results in a packaged, easily downloadable archive. Each analysis requires a Dovetail credit.

One credit for input files with total size less than or equal to 60GB, and two credits for input files with total size greater than 60 GB and less than 100 GB. If your input files exceed 100GB in total, please support@cantatabio.com.

Insights simplified.

The Dovetail Analysis Portal enables the streamlined analysis and interactive data browsing of NGS FASTQ files generated from Dovetail linked-read libraries.

The portal offers simplified and fast insights for supported workflows including

1. Somatic variant calling (human only)

2. Epigenetic feature calling (human and mouse only).

The portal delivers results in a summary report and packaged, easily downloadable archive. In addition, it offers interactive data browsing directly through the portal. Each analysis requires a Dovetail® Analysis Portal credit.

The analysis pipeline is fully supported and maintained by Dovetail Genomics. Should you have any inquiries, please refer to our FAQ below or contact support@cantatabio.com.

We support inter-AWS account file transfers for data upload and results delivery. Data delivered to your personal AWS S3 are not subject to the 10-day storage time through our portal. Please see our General FAQ for more information.

An infographic digital report with sections on Genome Epigenetics processes and Variant Detection, including contact maps, A/B compartments, chromatin loop counts, and chromatin loop visualization, alongside reports on structural variants, copy number variants, SNVs, insertions, deletions, and AI-driven interpretation.