Know the Facts About Bladder Cancer
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Clinical Impact of Informative and Actionable Results in Hereditary Cancer Testing
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Optimizing Patient Care after Miscarriage with a SNP – based Microarray
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Cell-free DNA screening for trisomies 21, 18, and 13 in pregnancies at low and high risk for aneuploidy with genetic confirmation.
Dar et al. 2022 AJOG publication
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Cell-free DNA screening for prenatal detection of 22q11.2 deletion syndrome
Dar et al. 2022 AJOG publication
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Panorama NIPT and Horizon Carrier Screen Patient Overview - Vietnamese
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Panorama NIPT and Horizon Carrier Screen Patient Overview - Spanish
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Panorama NIPT and Horizon Carrier Screen Patient Overview - Russian
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Panorama NIPT and Horizon Carrier Screen Patient Overview - Chinese
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Findings from the landmark SMART Study Teaser
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Life after a transplant: Tara’s organ health journey
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Tissue Sample Collection Instructions
Overview document on how Signatera collections a FFPE sample.
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Genetic Etiologies for Chronic Kidney Disease Revealed through a Next-Generation Renal Gene Panel
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Navigating the IVF Journey
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Early reduction in ctDNA is associated with overall survival (OS) on tebentafusp in previously treated metastatic uveal melanoma patients
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Circulating tumor DNA based molecular residual disease detection for treatment monitoring in advanced melanoma patients
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Signatera Patient Brochure: Discover a better way to help monitor your immunotherapy treatment
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Skin Cancer and Melanoma Awareness Month
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Panel Discussion: Emerging Trends & Opportunities for ctDNA MRD in Clinical Trials
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22q11.2 Deletion Syndrome: The Most Common Microdeletion Syndrome
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