Overview
Complete Genome Analysis
For the most comprehensive curated DNA analysis and interpretation, all presented in a compact Complete DNA Analysis Report, organized into the following categories:
| INHERITED TRAITS | INHERITED CONDITIONS | DISEASE SUSCEPTIBILITY | GENETIC ANCESTRY | ||||||
|---|---|---|---|---|---|---|---|---|---|
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Physical Appearance Nutrition Related Blood Related Drug Response Immune System Fitness Related Miscellaneous Traits
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Inherited Carrier Status Inherited Dominant Conditions Inherited X-Linked Conditions Actionable Conditions
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Autoimmune Diseases Cancers Cardiovascular Diseases Eye Related Diseases Female Specific Diseases Neurodegenerative Diseases Neuro-psychological Diseases Other Diseases |
Ancestry Composition Maternal Mitochondrial Paternal Y-Chromosome Haplogroup Distribution
|
Sample DNA Report Pages
Getting Started
Complete Genome Analysis provides a comprehensive assessment of your DNA.
Once your DNA data is stored in your Sequencing.com account, purchase this DNA report, and then click the app's 'Start' button. You'll receive your report in about 30 minutes.
If your DNA data is not already stored in your account, you can either import your data from a DNA test you've already taken (such as from 23andMe or AncestryDNA) or you can order one of our DNA tests.
You've already taken a DNA test |
You need a DNA test |
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| Our Universal DNA Compatibility enables this app to work with DNA data from almost any genetic test including 23andMe, Ancestry, MyHeritage, FTDNA, and genome sequencing. | Our clinical-grade 30x Whole Genome Sequencing test obtains data on 100% of your genome. |
Free DNA Data Upload
Compatible with data from almost all DNA tests and genome sequencing services.
| Test Compatibility | Format Compatibility | Variant Compatibility | Reference Genome Compatibility | |||
|---|---|---|---|---|---|---|
| Whole Genome Sequencing | FASTQ and FQ | SNP / SNV (Single Nucleotide Variants) |
hg38 / GRCh38 | |||
| Exome Sequencing | FASTA and FA | hg19 / GRCh37 | ||||
| Ultimate DNA Test | BAM | hg18 / GRCh36 | ||||
| 23andMe | SAM | hg17 / GRCh35 | ||||
| AncestryDNA | CRAM | |||||
| MyHeritage | VCF | |||||
| Dante Labs | Genome VCF (gVCF and GVCF) | |||||
| Nebula Genomics | TXT | |||||
| Genes for Good | CSV | |||||
| Living DNA | TAB | |||||
| HomeDNA | gz and zip compressed files | |||||
| FTDNA | almost all other genetic data formats | |||||
| Silverberry Genomix | ||||||
| Toolbox Genomics | ||||||
| Full Genomes | ||||||
| Color | ||||||
| New Amsterdam Genomics | ||||||
| 24Genetics | ||||||
| Vitagene | ||||||
| Helix | ||||||
| Genos | ||||||
| tellmeGen | ||||||
| GSA | ||||||
| Axiom | ||||||
| almost all other genetic tests |
Overview
Sequencing.com is the world's largest DNA App Store. We have an app for almost everything that can be determined from your genes.
Additional DNA Reports by Complete Genome Science
 Genetic Ancestry + Haplogroups |
 Medication & Drug Response |
 Disease Susceptibility |
 Carrier Status |
 Nutrigenomics |
 Traits |
 Physical Appearance |
 Immune System |
 Blood Traits & Conditions |
Disclaimer
The genetic analysis and statements that appear in this app, assessment, and report have not been evaluated by the United States Food and Drug Administration. The Sequencing.com website and all software applications (Apps) that use Sequencing.com's website, as well as Sequencing.com's open Application Programming Interface (API), are not intended to diagnose, monitor, treat, cure, prevent nor alleviate any disease.
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