Already sequenced? Skip the kit. Run the reports.

If you already have your DNA file, Mosaic builds your reports from it. Create a free account, upload your file, and run the report in the platform.

Registration and upload are free. You pay only when you run a report.

Three simple steps.

Step 01
Create a free account
Takes about a minute. Email and password, nothing else.
Step 02
Upload your file
PHI-safe, encrypted in transit and at rest. Upload .txt, .csv, .vcf, .vcf.gz, or .gz up to 300 MB; the file is checked before it goes up.
Step 03
Run your report
Once your file clears the quality check, buy the report in the platform. It attaches to your file.

Consumer raw-genotype files, sequencing-service exports, and whole-genome VCFs.

Consumer raw genotype

TXT / CSV

SNP-chip files: about 600,000 positions. The report reads everything the chip captured and names any insight it could not.

Sequencing-service genotype

TXT

Exports already processed into rsID-keyed genotype calls.

Whole-genome sequencing

VCF / VCF.gz

Single-sample SNP/indel calls from any clinical-grade WGS provider.

Smaller vendors (Vitagene, Genos, and others) usually work too. Tell us about your file and we’ll confirm it before you upload.

Six kinds of file need a different export first

Structural-variant VCFs. Files ending in .sv.vcf.gz (e.g. Manta output) describe large rearrangements, not the SNP/indel calls Mosaic reports use. Send the "snp-indel" companion file from the same vendor.
Multi-sample VCFs. Files containing more than one person’s data. Mosaic processes single-sample uploads.
Clinical pharmacogenomic gene-CSVs. Files structured as Gene,Variant,Result (some clinical labs export this way). Mosaic reads rsID-keyed raw genotype data, not interpretation summaries.
JSON, XML, or HTML files. These are interpretation outputs. The underlying raw data file is what Mosaic reads.
Gzipped non-VCF files. Decompress a .txt.gz or .csv.gz first, then upload the .txt or .csv. (A .vcf.gz is fine as is; that’s the standard.)
Files over 300 MB, or that fail the integrity check. The current cap is 300 MB. A file that fails the integrity check needs a fresh export from your vendor.

Every finding comes from your file as read. Where a position is missing, the report says so. How we handle gaps

$199

per qualifying upload

Whole-genome VCF or SNP-chip file. Add any deep-dive report to the same file, from $49 each.

On a SNP-chip file: the chip covers about 600,000 of 3 billion positions, so some insights are out of reach. Your report names each one.
Want all of it? A Mosaic kit reads every position at 30× depth, once, for $895. See the kit
Practitioner? Create a free provider account to see wholesale pricing.