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The Ambry Blog

Explore clinical deep dives, patient stories, and a look behind the scenes of our scientific research and technologies. Filter by topic to find the insights and stories that matter to you.

Latest Articles

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November 15, 2024

How the Ambry Patient for Life™ Program Minimizes the Need for Provider-Initiated Exome Reanalysis Requests

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Melissa Holman, Genomic Science Liaison
One of the unique benefits of exome testing is the ability to return to the data from the initial analysis and reevaluate it for new,…
Genetic Testing
Genetic Testing Accuracy
Multigene Panel Testing
Tag
VUS
Whole Exome Sequencing
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October 31, 2024

Striking the Perfect Balance in Designing Hereditary Cancer Tests: The Ambry Approach

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Jessica Grzybowski, Lead Genetic Counselor, Reporting – RNA, Ambry Genetics
Ambry’s balanced approach to designing hereditary cancer tests ensures our panels remain relevant and impactful, helping clinicians manage hereditary cancer risk with confidence.
Genetic Testing
Genetic Testing Accuracy
Hereditary Cancer
Multigene Panel Testing
Variant of Unknown Significance
VUS
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October 31, 2024

Early Detection in Action: Angie’s CARE Story

One CARE patient’s story demonstrates the power of proactive care and comprehensive high-risk screening.
BRCA1 & 2
Breast Cancer
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October 17, 2024

The Evolution of Hereditary Cancer Testing: Why Pan-Cancer Panels Are the Future of Genetic Risk Assessment

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Elizabeth Chao, Laboratory Director, Ambry Genetics
Pan-cancer panels offer more comprehensive diagnoses, personalized risk assessments, and targeted prevention and treatment strategies.
BRCA1 & 2
Genetic Testing
Genetic Testing Accuracy
Hereditary Cancer
Multigene Panel Testing
Ovarian Cancer
Variant of Unknown Significance
VUS
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October 16, 2024

Polyposis Explained: Solving the Mystery with RNA Testing

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Jessica Scott, Genomic Science Liaison II
Genetic counselor Karen Powell shares a case study of her first patient with RNA testing, which helped identify familial adenomatous polyposis (FAP).
Colorectal Cancer
Genetic Testing
RNA
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October 10, 2024

Pioneering New Research to Support Rare Disease Patients and Families

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Elizabeth Chao, Laboratory Director, Ambry Genetics
Dr. Elizabeth Chao explains how Ambry’s collaboration with PacBio to participate in the GREGoR Consortium to unlock the mysteries of the genome.
Clinical Research
Genetic Testing
Genetic Testing Accuracy
Next Generation Sequencing
Novel Genes
Scientific Research