See what your file can tell you, before you pay
Choose the DNA file you already own. It is read on your device, in this page. Nothing is uploaded, and you do not need an account to find out what is in it.
Read on your device. Nothing is uploaded, no account is made.
Reading on your device…
Reading your file on your device…
That's . We can build your report from it.
Keep this tab open. Your file is still only on this device.
- Account
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Once you confirm your address, upload your file from your account. Your report credit stays there until you use it. Upload from your account
Uploading your file
Over an encrypted connection, to storage in Finland. Your analysis page opens when it is done.
One price for everything below.
One-time, yours to keep. Your file is still on your device: you upload it after checkout, over an encrypted connection, to storage in Finland.
What your file reads
Read on your device. Nothing is uploaded.
What it can tell you
What it can't
A chip reads a fixed set of common spots, so the rare-variant panels need a sequenced genome. We tell you this now rather than after you have paid.
That's : aligned reads.
This is exactly what the Deep Read pharmacogenomic panel needs: 29 targets read at base level, including the CYP2D6 star-alleles a normal VCF cannot reliably call. The standard report is built from a VCF/gVCF, so aligned reads sit alongside one rather than replacing it.
Deep Read needs standard-depth reads. A low-pass file, MyHeritage's own sequencing download among them, is read about twice over rather than thirty times, which is too thin to call these genes from. We measure the depth and stop rather than guess.
A CRAM also needs the exact reference assembly it was compressed against, not merely the same genome build. We hold the common ones and check yours before taking any money, so an assembly we cannot read is refused rather than charged for.
What the pair covers
The bundle is the whole-genome report plus the Deep Read panel. The report is built from a variant file and the panel from your reads, so it takes both. Most sequencing providers hand you both in the same download.
Nothing was uploaded, and you have not paid anything. We would rather turn a file away here than sell you a report it cannot support.
This check ran on your device from your file's header. We confirm the full file after upload, and never charge for a report we cannot build.
This check read your whole file on your device. We confirm it again after upload, and never charge for a report we cannot build.