GENOMIC HEALTH

DNA Reports for Better Care

See risk, trait, and variant data in plain language for care teams and patients.

DNA kit, sequencing cartridge, and glass helix in a moody genomics lab

TOPICS

From the journal

What a variant is, and why it matters in a report.

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GUIDE

Variant Basics

What a variant is, and why it matters in a report.

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GUIDE

Family Risk

How family history and DNA data work together.

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TRENDS

Drug Response

When genes may shape dose, side effects, and drug choice.

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TIPS

Study Design

Clean ways to use sequencing data in research.

average report turn time

24 hrs

average report turn time

reports checked by specialists

98%

reports checked by specialists

gene and trait markers covered

150+

gene and trait markers covered

The Map

Community

Customer notes

Verified

The report was easy to read, and my doctor could use it the same day.

D

Dr. Elena Park

Medical Geneticist, Northbridge Clinic

Verified

I saw the risk points fast, without having to decode hard lab terms.

M

Marcus Reed

Primary Care Physician, Lakeview Health

Verified

Their notes made family history and DNA data fit together.

S

Sofia Alvarez

Research Lead, Weston Genomics Lab

LAB NOTES

Lab Notes and Case Files

A plain read on what reports can and cannot tell you.

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FEATURE

How DNA Fits Care Plans

A plain read on what reports can and cannot tell you.

Macro of a breast-health exam room with robe, tray, and privacy curtain.
0201

BRCA1 and BRCA2

What these genes mean for breast and ovarian risk.

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0302

Drug Response Notes

How genes can change drug choice and dose.

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WIDE READ

Prenatal Carrier Checks

What couples learn before pregnancy.

High-angle family-history tabletop with acrylic branches, sample tubes, ring box, and linen.
05GUIDE

Family History Review

Turn notes from three generations into one simple map.

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06TIPS

Nutrition Gene Signals

Read links with food response, vitamin use, and weight.

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07TIPS

Fitness and Recovery

See how genes may shape endurance, power, and rest.

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08LAB

Research Cohort Sets

Use clean variant data for study groups and papers.

Questions

Common questions

Quick answers before visitors choose a product, service, or next step.

01What does Life Genomic do?+

We test DNA and read variants in plain language so patients, clinicians, and teams can use the results with more confidence.

02Who are your services for?+

We serve patients, doctors, clinics, and research teams that need clear genetic data for care, review, or study work.

03Do you offer hereditary risk reports?+

Yes. We show inherited risks, gene links, and next steps in a format that is easy to read and simple to share.

04Can clinicians use your reports?+

Yes. Reports are built for quick review, with variant notes, trait data, and care-friendly summaries for the whole team.

05Do you support research teams?+

Yes. We help teams with sequencing reads, clean variant tables, and data that is easier to sort, compare, and use.

06Do you include wellness traits?+

Yes. We can report on traits tied to food response, sleep, caffeine, and fitness cues in a plain summary.

Get lab notes

Get short notes on DNA testing, variant reports, and new studies, sent to your inbox each week.