Change the course of a disease before it starts.

Change the course of a disease before it starts.

Change the course of a disease before it starts.

Whole-genome data enriched with a lifetime of clinical records, synthesized for the physician who can act on it.

Whole-genome data enriched with a lifetime of clinical records, synthesized for the physician who can act on it.

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Read the Science

Jordan

McCallister

45 • Female

5’3”

127lbs

Penicillin

Sulfonamides

Codeine

Gluten

Hashimoto’s

Perioral dermatitis

Overview

Labs + Diagnostics

Genetics

Rx + Supplements

3

Encounters + Notes

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Patient Focus

45 year-old female, preventive and longevity-oriented individual seeking sustained energy, optimized sleep, and thyroid support.

General Overview

Context of Care

Longitudinal care across UCSF/MarinHealth since 2019 with Endocrinology/Dermatology; active problems: acquired hypothyroidism , thyroid nodule, perioral dermatitis , history of hyperparathyroidism with hypocalcemia, benign skin lesions; personal Hashimoto’s, maternal rosacea, grandmother thyroidectomy (reason unknown).

Course/response: flares build over 1–2 weeks and resolve only with antibiotics or reduced thyroid dose; TIROSINT 120→88 mcg briefly cleared for 2–3 weeks; cheek culture normal flora; using ivermectin 1% cream daily; ~90% improved at intake.

Triggers/psychosocial: sunburn, makeup, and red wine worsen flares; tolerates only light moisturizer and prefers natural products; stress has high daily impact and flares are embarrassing; uses meditation and exercise for coping.

Thyroid therapy/trajectory: on TIROSINT (levothyroxine) plus liothyronine; TSH largely suppressed in 2022–2025, then elevated with low‑normal Free T4 in 01/2026 while on TIROSINT 75 mcg daily.

Thyroid/Parathyroid findings: 02/2022 US—heterogeneous thyroid with 0.7 cm TI-RADS 4 right nodule (<1 cm, no follow-up) and 0.6 cm focus possibly parathyroid; 03/2023 US—no discrete thyroid nodules; persistent small oval structure posterior to right thyroid (possible parathyroid adenoma vs lymph node). History of hyperparathyroidism/hypocalcemia with PTH 94 pg/mL (10/2022) and later normal values; calcium intermittently low‑normal (e.g., 8.5 mg/dL in 09/2024).

Sex steroid profile: marked estradiol/testosterone elevations on 10/27/2023 with estradiol decreased 11/2023; on testosterone gel with total testosterone 37 ng/dL (04/03/2025) and 80 ng/dL (01/05/2026).

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hypothyroidism

perioral dermatitis

TIROSINT 120→88 mcg

Ivermectin 1%

Patient History

See All Events

Jan 12, 2026

Infectious disease screening

HIV • Syphilis • HBV • HCV

All non-reactive

Jan 05, 2026

Hormone therapy follow-up

Testosterone gel • Total T 80 ng/dL

Total T 80 ng/dL

Jan, 2026

Thyroid labs - TSH now elevated

TIROSINT 75 mcg • Free T4 low-normal

TSH elevated

Late 2025

Skin cleared with thyroid dose

TIROSINT 120 → 88 mcg • Skin clear 2-3 weeks

Perioral dermantitis

Genetics

Polygenic Risk Score (PGS)

640 traits scored

227 high risk

Highest Risk Categories

Cancer

Cardiovascular Disease

Digestive System Disorder

Genetic Findings

APOE

Pathogenic

HLA

Likely Pathogenic

MTHFR

Likely Pathogenic

Pharmacogenomics (PGX)

Levothyroxine

AB123 • Lorem ipsum

Adjust Dose

Sertraline

AB123 • Lorem ipsum

Monitor

Metformin

AB123 • Lorem ipsum

Avoid

Rx + Supplements

Medications

Levothyroxine

50mcg

Daily

Active

Levothyroxine

50mcg

Daily

Active

Over the counter

Vitamin C

500mg

Daily

Active

Ibuprofen

400mg

As needed

Active

Zyrtec

10mg

Daily

Stopped

Supplements

Vitamin D3

5,000 IU

Daily

Active

Vitamin K2

100 mcg

Daily

Paused

Ferrous Bisglycinate

25 mg

Daily

Active

Magnesium Glycerinate

400 mg

Daily

Inconsistent

Selenium

200 mcg

Daily

Stopped

The Gap

Genotype, meet phenotype.

Genotype, meet phenotype.

A lifetime of your patient's data—scattered, unsynthesized, no genome. Or a genome with no clinical record to give it meaning. Profile is the only tool that joins both.

Get Started

The Gap

Genotype, meet phenotype.

A lifetime of your patient's data—scattered, unsynthesized, no genome. Or a genome with no clinical record to give it meaning. Profile is the only tool that joins both.

Get Started

In Your Practice

In Your Practice

Whole-genome sequencing and a lifetime of your patient's clinical records, synthesized into one view—ready before you open the chart.

Whole-genome sequencing and a lifetime of your patient's clinical records, synthesized into one view—ready before you open the chart.

2,000+ patients synthesized

01

A new patient intake

Profile replaces the clipboard with a guided intake that captures history, symptoms, and consent in the patient's own words — then hands your staff a completed record instead of a stack to transcribe.

02

We retrieve the record

A lifetime of labs, notes, imaging, and prescriptions pulled across 600,000+ providers through CareQuality and direct EHR integration.

03

Genome meets record

50GB+ of whole-genome data, normalized and scored against the patient's actual genetic ancestry, then read against their clinical history.

04

Ready before the visit

One synthesized view, seamlessly presented. Not a 400-page report—the genetics, the clinical history, and the findings that change what you do next, in a single place.

The raw material

The raw material

Most "genetic testing" reads about 0.1% of the genome.

Most "genetic testing" reads about 0.1% of the genome.

Consumer chips and most clinical panels genotype a few hundred thousand pre-selected markers. Profile sequences the whole thing — 50GB+ per patient, thousands of times more genetic information — because you can't score what you never read.

Consumer chips and most clinical panels genotype a few hundred thousand pre-selected markers. Profile sequences the whole thing — 50GB+ per patient, thousands of times more genetic information — because you can't score what you never read.

Why it’s different

Why it’s different

Most polygenic scores break on non-European genomes. Ours don't.

Most polygenic scores break on non-European genomes. Ours don't.

The reference cohorts that produced the published scores were overwhelmingly European. Applied to anyone else, they lose accuracy quietly — and in the direction of missing risk. Profile resolves genetic ancestry before scoring, so the number means something for the patient it describes.

The pipeline

The pipeline

Five stages, one normalized genome.

Five stages, one normalized genome.

Preprocessing, ancestry, polygenic risk across 640+ traits, pharmacogenomics on the active medication list, and clinical variants classified against ClinVar, gnomAD, and ClinGen.

How we handle uncertainty

How we handle uncertainty

Nothing is generated. Everything resolves to a source.

Nothing is generated. Everything resolves to a source.

Every finding traces back to a curated variant database, a published score, or a line in your patient's own record. Variants of uncertain significance stay labeled uncertain. You can follow any statement on the screen to where it came from.

The synthesis is the input. The medicine is yours.

Profile doesn't diagnose and doesn't recommend. It assembles what's knowable about one patient and hands it to the person qualified to act on it.

The synthesis is the input. The medicine is yours.

Profile doesn't diagnose and doesn't recommend. It assembles what's knowable about one patient and hands it to the person qualified to act on it.

Leadership Team

Leadership Team

Our CMO still sees patients...

Our CMO still sees patients...

Profile was designed by people who have to use it—a practicing clinician, a molecular pathologist, and a founder who has spent years being the patient whose diagnosis took too long. It's built for a real visit because it was built inside one.

Dr. Brendan Cochran, CMO

Clinician and founder of Interactive Health Clinic. International lecturer in longevity medicine, chronic disease, integrative oncology.

Dr. Tushar Chakravarty, CSO

Physician and molecular pathologist (UCSF). Built a genomics lab from the ground up at Loma Linda. Biochemistry, Johns Hopkins.

Quinton Poncelet, CAIO

CERN physicist and AI researcher; high-energy physics and advanced simulation, now powering Profile's genotype × phenotype pipeline.

Mandi Bateman, CEO

Repeat founder; scaled products across health and edtech. And the patient—living with autoimmune disease, she sees the problem from the inside.

The Window

The forty years from forty.

Adults 40–64 are a third of the population and 40% of U.S. medical spending. They're already in your practice, already asking what to do.

Bring Profile to your practice

The Window

The forty years from forty.

Adults 40–64 are a third of the population and 40% of U.S. medical spending. They're already in your practice, already asking what to do.

Bring Profile to your practice

Genetic intelligence for clinicians. Whole-genome sequencing plus a lifetime of records, synthesized into one view and delivered into your EHR.

Disclaimer: Profile Health provides clinical decision support and does not diagnose or recommend treatment. All clinical decisions remain with the treating physician.

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