We help families organize full 30x whole-genome sequencing data, preserve downloadable raw files, and prepare complete genomic archives for future hereditary review as science continues to advance.
Sequence Me is a nonclinical genome data preservation and concierge service. It is not medical advice, diagnosis, treatment, or genetic counseling.
Most consumer DNA tests give you a fraction of your genome. We help families preserve the complete picture — every chromosome, every read — stored for life.
Full 30x whole-genome sequencing produces raw FASTQ, aligned BAM/CRAM, and variant-called VCF files — the same data used in clinical research.
Organize genome data for parents and children in one place, supporting hereditary pattern review with qualified professionals when you choose to pursue it.
Genomic science improves every year. Having your raw data preserved means you can reanalyze it as new discoveries emerge — without resampling.
Your genome files are delivered directly to you on encrypted media. No subscription required. No third-party access without your explicit consent.
From intake to archive delivery, we guide your family through every step.
Complete the family genome intake form. We use privacy-conscious naming conventions and collect only what's needed to coordinate sequencing for each family member.
We coordinate with Sequencing.com to place your family's kit order. Kits ship directly to your address with clear instructions for each member.
Follow the included guidance for saliva or cheek swab collection. Activate each kit online and return using the prepaid shipping materials.
Your samples are processed using 30x whole-genome sequencing. Results typically take several weeks. We monitor progress and notify you when data is ready.
We download, organize, and package your complete genome files into a structured archive. Data is delivered on encrypted USB or SSD with a full readme and inventory.
A complete, organized genome archive — yours to keep, download, and reanalyze for life.
FASTQ, BAM/CRAM, and VCF files from 30x whole-genome sequencing for each family member.
Clearly labeled directories for raw reads, aligned data, variant calls, reports, and documentation.
Data delivered on hardware-encrypted media. Password provided separately via secure channel.
Plain-language documentation explaining every file, its format, and how to access it.
Optional downstream package formatted for tools like IGV, GATK, or clinician-supplied pipelines.
Parent-child relationships documented in the archive structure for hereditary pattern context.
Genome data is among the most sensitive personal information that exists. We minimize identifiers at every step.
We default to privacy-conscious identifiers like initials and birth year.
Example folder structure:
MR-1985 / GR-2020 / AR-2022
Full names are never used in file names, folder names, or metadata unless you explicitly request it.
Intake collects only what's needed for kit coordination and delivery. We do not store Social Security numbers, insurance information, or clinical records.
Your genome data is delivered directly to you. We do not retain copies after delivery unless you request backup storage.
Begin the process for yourself or your family. Complete the form below and we'll follow up within 48 hours.