Which whole genome sequencing providers do you support?

Any provider is supported if it gives you a usable, single-sample whole-genome VCF or VCF.GZ file. That includes exports from providers such as Nebula Genomics, Dante Labs, Sequencing.com, Nucleus Genomics, DNA Complete, and others. Provider branding does not matter; the file format and data quality do.

Which Genomisaur reports work with WGS data?

Every report type: Starter, Immune, and Full Health Reports, plus Family Starter and Family Full Reports. For a family report, either or both parents may use WGS, and the other parent may use WGS or a supported consumer-array file.

What WGS file should I upload?

Upload a single-sample .vcf or .vcf.gz file. GRCh37 and GRCh38 inputs are supported. VCF.GZ is recommended because it is much faster and more reliable to upload. BAM, CRAM, FASTQ, gVCF, and multi-sample VCF files are not currently supported.

Do you sell whole genome sequencing kits?

No. Genomisaur analyzes WGS data you already have. We do not collect a new sample or perform sequencing, so you can choose any sequencing provider and bring the resulting VCF to us.

WGS processing adds $20 per uploaded genome because whole-genome files require substantially more preparation and quality control. An individual report has one WGS processing fee. A family report adds one fee for each parent who uploads WGS.

Is a WGS-based Genomisaur report a clinical diagnosis?

No. Genomisaur reports are informational and are not a substitute for clinical genetic testing, diagnosis, or medical advice. Discuss health or carrier findings with a qualified healthcare provider or genetic counselor.

Bring your own whole genome

Your whole genome already has somewhere to go.

Upload a single-sample WGS VCF or VCF.GZ from any sequencing provider and use it with every Genomisaur report—individual health or two-parent preconception.

WGS processing: +$20 per uploaded genome

Input

Any WGS provider

Portable file

Single-sample .vcf or .vcf.gz

Every health report

Every family report

Provider-independent by design

The file matters. The logo does not.

Genomisaur reads the standard VCF export, so you are not locked to a sequencing company. These are examples—not a complete provider list.

Nebula GenomicsDante LabsSequencing.comNucleus GenomicsDNA CompleteVeritasAny other WGS provider

One WGS file. Every report type.

Choose by the questions you want answered, not by where your genome was sequenced.

Individual health reports

Use WGS with Starter, Immune, or Full Health Reports for polygenic risk scores and trait predictions.

Starter Health Report
Immune Health Report
Full Health Report

See health report options

Two-parent family reports

Use WGS with Family Starter or Family Full. Mix WGS and array data between parents, or upload WGS for both.

WGS + WGS supported
WGS + consumer array supported
Family Starter and Family Full supported

See family report options

Before you upload

A precise compatibility check

We support the common portable output from WGS—not every file generated during sequencing.

VCF or VCF.GZ

Upload a .vcf or compressed .vcf.gz file. VCF.GZ is recommended.

One sample

The VCF must contain one person, not a joint or multi-sample call set.

GRCh37 or GRCh38

Both common human genome builds are supported and checked during preparation.

Up to 500 MB

Compress large VCFs before uploading for faster, more reliable transfer.

Not currently accepted: FASTQ, BAM, CRAM, gVCF, or multi-sample VCF files.