MyOme
Whole genome sequencing platform for polygenic disease risk prediction
- Sector
- Biotech
- Federal grants
- None on recordNo awards found in SBIR/STTR, NIH, NSF or DoD records.
- Private capital raised
- None on recordNo Form D filings on SEC EDGAR. Some raises are not filed.
- Federal contracts
- None on recordNo federal contract awards found.
- Granted patents
- 1
- 29 pending · first 2026
- Rank in peer group#73 of 342
Capital timeline
No federal awards or Form D filings are on record for this company.
Many early companies raise without filing a Form D, or have not yet won a federal award. New records appear here as the sources update.
Checked: SEC EDGAR Form D through Oct 23, 2026; SBIR and STTR awards through Oct 21, 2026; USAspending contract awards
Founder? Add funding contextStanding among 342 peers
Line = medianBiotech · Platform
- Granted patents#73 · top 21%
Cumulative measures favor older companies. Rankings describe position today, not outcome. Below the median, ranks show as a band rather than a number.
Founders and team
No founders are linked to this company yet.
Founders appear once a person is matched to the company through its own patents, grants or filings. We never infer people from social profiles.
Checked: USPTO inventors; federal award principal investigators; SEC Form D related persons · Oct 23, 2026
Claim this profile to add your teamWhat it has protected
USPTO · 1 granted of 30- GrantedPolygenic Risk Score For In Vitro FertilizationUSPTOUS 12,718,953
- PendingSample Matching Using Select Single Nucleotide Polymorphisms Within Target RegionsUSPTOApplication 19209683
- PendingApplication Of Local Ancestry Inference And Polygenic Risk Scores For Prediction Of Complex Disease Risk In Admixed IndividualsUSPTOApplication 19176704
Show all 30 patent records
- Polygenic Risk Score For In Vitro FertilizationAug 25, 2026 · US 12,718,953Granted
- Sample Matching Using Select Single Nucleotide Polymorphisms Within Target RegionsNov 6, 2025 · Application 19209683Pending
- Application Of Local Ancestry Inference And Polygenic Risk Scores For Prediction Of Complex Disease Risk In Admixed IndividualsOct 23, 2025 · Application 19176704Pending
- Approach For Early Detection Of Disease Combining Multiple Data SourcesAug 7, 2025 · Application 19188681Pending
- Methods to Simulate Prospective Embryo Genotypes and Approximate Disease Occurrence RiskApr 24, 2025 · Application 18695411Pending
- Systems And Methods For Identification Of Structural Variants Based On An AutoencoderMar 20, 2025 · Application 18959135Pending
- System For Predicting Genetic Diseases And Conditions Using A Neural Network That Is Trained On Data Aligned To A Reference Genome Using Graph Attention MechanismsFeb 6, 2025 · Application 18798187Pending
- Use Of Non-error-propagating Phasing Techniques And Combination Of Allelic Balance To Improve Cnv DetectionDec 21, 2023 · Application 18251096Pending
- Polygenic Risk Score For In Vitro FertilizationNov 17, 2022 · Application 17765073Pending
- Use Of Gene Expression Data And Gene Signaling Networks Along With Gene Editing To Determine Which Variants Harm Gene FunctionJun 9, 2022 · Application 17599343Pending
- System For Predicting Genetic Diseases And Conditions Using A Neural Network That Is Trained On Data Aligned To A Reference Genome Using Graph Attention MechanismsApplication PCTUS2023062258Pending
- Sample Matching Using Select Single Nucleotide Polymorphisms Within Target RegionsApplication 63384046Pending
- Approach For Early Detection Of Disease Combining Multiple Data SourcesApplication 63381198Pending
- Application of Local Ancestry Inference and Polygenic Risk Scores for Prediction of Complex Disease Risk in Admixed IndividualsApplication 63379395Pending
- Methods To Simulate Prospective Embryo Genotypes And Approximate Disease Occurence RiskApplication PCTUS2022077123Pending
- Systems And Methods For Identification Of Structural Variants Based On An AutoencoderApplication 63346096Pending
- System For Predicting Genetic Diseases And Conditions Using A Neural Network That Is Trained On Data Aligned To A Reference Genome Using Graph Attention MechanismsApplication 63324536Pending
- Use Of Non-error-propagating Phasing Techniques And Combination Of Allelic Balance And Depth Of Read Signals To Improve Cnv Detection, Genome Reconstruction, And Variant InterpretationApplication PCTUS2021057400Pending
- Methods To Generate Possible Embryo Genomes And Approximate Recurrence RiskApplication 63248749Pending
- Polygenic Risk Score For In Vitro FertilizationApplication PCTUS2020053514Pending
- System For Predicting And Reducing Recurrence Risk Of DiseaseApplication 63062044Pending
- Use Of Gene Expression Data And Gene Signaling Networks Along With Gene Editing To Determine Which Variants Harm Gene FunctionApplication PCTUS2020025670Pending
- Ngs-based Aneuploidy Detection Using Hmm Method With Support For MosaicismApplication PCTUS2026014564Pending
- Simulated Embryonic Genetic ProfileApplication PCTUS2026010327Pending
- Ngs-based Aneuploidy Detection Using Hmm Method With Support For MosaicismApplication 63756647Pending
- Simulated Embryonic Genetic ProfileApplication 63742575Pending
- Approach For Early Detection Of Disease Combining Multiple Data SourcesApplication PCTUS2023077932Pending
- Sample Matching Using Select Single Nucleotide Polymorphisms Within Target RegionsApplication PCTUS2023079775Pending
- Application Of Local Ancestry Inference And Polygenic Risk Scores For Prediction Of Complex Disease Risk In Admixed IndividualsApplication PCTUS2023076737Pending
- Systems And Methods For Identification Of Structural Variants Based On An AutoencoderApplication PCTUS2023023529Pending
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Regulatory activity · Biotech
- New Animal Drugs; Approval of New Animal Drug Applications; Withdrawal of Approval of New Animal Drug Application; Change of SponsorFood and Drug Administration
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- Medical Devices; General Hospital and Personal Use Devices; Classification of the Infant Supine Sleep SystemFood and Drug Administration
Rules are matched to sector, not to company. Recent activity in a sector is context rather than a signal about this business — until rules are matched to what a company actually builds, the section is shown as context and nothing more.
Sources
Federal grants from SBIR/STTR, NIH, NSF and DoD records. Federal contracts from USAspending.gov. Private capital from SEC Form D. Patents from USPTO. Publications from OpenAlex. Regulatory activity from the Federal Register. Press matched on company name.
How to read this page
Figures show associations in public records, not causes or predictions. Nothing here is investment advice. An em-dash means no record was found under this company's name, not that none exists.
Data freshness
SEC Form D filings through . SBIR and STTR awards through .