---
title: Two Must-See Liquid Biopsy Poster Videos From AMP 2018
description: At AMP’s Annual Meeting two poster presentations on NGS-based liquid biopsy assays stood out. Both presenters described how they work to reliably detect pathogenic variants at extremely low allele frequencies – efforts critical to the clinical adoption of NGS-based liquid biopsy assays.
image: https://blog.seracare.com/hubfs/Imported_Blog_Media/Video%20Analytical%20Validation%20516x-1.jpg
---

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# Two Must-See Liquid Biopsy Poster Videos From AMP 2018

Posted by [Sam Blier](https://blog.seracare.com/ngs/author/sam-blier) on Dec 7, 2018 12:00:00 AM

 

[![Video Use Molecular 516x](https://blog.seracare.com/hs-fs/hubfs/Imported_Blog_Media/Video%20Use%20Molecular%20516x.jpg?width=325&name=Video%20Use%20Molecular%20516x.jpg)](https://www.seracare.com/resources-and-education/videos/use-molecular-identifiers-targeted-ngs-enable-variant-detection-below-1-allele-frequencies-ccfdna/)

Of the many fantastic posters presented at AMP’s Annual Meeting in San Antonio, two concerning NGS-based liquid biopsy assays stood out. Both presenters described how their organizations are working to reliably detect pathogenic variants at extremely low allele frequencies – efforts critical to the clinical adoption of NGS-based liquid biopsy assays.

Swift Biosciences presented some very interesting data on molecular identifiers (MIDs) that enable accurate variant detection below 1% AF in ctDNA. They used the **[Seraseq ctDNA Reference Material v2](https://www.seracare.com/Seraseq-ctDNA-Reference-Material-v2-AF025-0710-0206/)** to test their assay’s limit of detection. **[Click here to download the poster and watch](https://www.seracare.com/resources-and-education/videos/use-molecular-identifiers-targeted-ngs-enable-variant-detection-below-1-allele-frequencies-ccfdna/)** Swift’s Francesco Criscuolo explain how Swift’s MID technology can improve NGS data analysis with his poster *Use of Molecular Identifiers and Targeted NGS to Enable Variant Detection Below 1% Allele Frequencies in Circulating Cell-Free DNA*.

[![Video Analytical Validation 516x-1](https://blog.seracare.com/hs-fs/hubfs/Imported_Blog_Media/Video%20Analytical%20Validation%20516x-1.jpg?width=325&name=Video%20Analytical%20Validation%20516x-1.jpg)](https://www.seracare.com/resources-and-education/videos/analytical-validation-oncomine-breast-cfdna-assay-v2/)

Another compelling poster was presented by MolecularMD’s Dr. WeiHua Liu. Her team took a methodical approach to validating the Oncomine Breast cfDNA Assay v2 and used both the **[Seraseq ctDNA Complete Mutation Mix](https://www.seracare.com/Seraseq-ctDNA-Complete-Mutation-Mix-AF01-0710-0532/)** and **[ctDNA Mutation Mix v2](https://www.seracare.com/Seraseq-ctDNA-Mutation-Mix-v2-AF1-0710-0140/)** reference materials to determine the amount of DNA input needed to reproducibly detect SNVs at 0.1% AF. **[Check out her poster presentation video](https://www.seracare.com/resources-and-education/videos/analytical-validation-oncomine-breast-cfdna-assay-v2/)**, titled *Analytical Validation of Oncomine Breast cfDNA Assay v2,* to learn more about their methodology.

Want to learn more about our QC and validation solutions for NGS-based liquid biopsy assays? **[Click here](https://www.seracare.com/Controls---Reference-Materials-NGS-Somatic-Cancer-Liquid-Biopsy/).**

---

**To watch the videos and download these free posters, click each title below:**

[![Analytical Validation of Oncomine Breast cfDNA Assay v2 poster](https://blog.seracare.com/hs-fs/hubfs/Imported_Blog_Media/Analytical%20Validation%20of%20Oncomine%20Breast%20cfDNA%20Assay%20v2%20poster.png?width=250&name=Analytical%20Validation%20of%20Oncomine%20Breast%20cfDNA%20Assay%20v2%20poster.png)](https://www.seracare.com/resources-and-education/videos/analytical-validation-oncomine-breast-cfdna-assay-v2/)  **[Analytical Validation of Oncomine Breast cfDNA Assay v2](https://www.seracare.com/resources-and-education/videos/analytical-validation-oncomine-breast-cfdna-assay-v2/)**

[![Use of Molecular Identifiers and Targeted NGS to Enable Variant Detection Below 1 Allele Frequencies in Circulating Cell-Free DNA poster](https://blog.seracare.com/hs-fs/hubfs/Imported_Blog_Media/Use%20of%20Molecular%20Identifiers%20and%20Targeted%20NGS%20to%20Enable%20Variant%20Detection%20Below%201%20Allele%20Frequencies%20in%20Circulating%20Cell-Free%20DNA%20poster.png?width=250&name=Use%20of%20Molecular%20Identifiers%20and%20Targeted%20NGS%20to%20Enable%20Variant%20Detection%20Below%201%20Allele%20Frequencies%20in%20Circulating%20Cell-Free%20DNA%20poster.png)](https://www.seracare.com/resources-and-education/videos/use-molecular-identifiers-targeted-ngs-enable-variant-detection-below-1-allele-frequencies-ccfdna/)

**[Use of Molecular Identifiers and Targeted NGS to Enable Variant Detection Below 1% Allele Frequencies in Circulating Cell-Free DNA](https://www.seracare.com/resources-and-education/videos/use-molecular-identifiers-targeted-ngs-enable-variant-detection-below-1-allele-frequencies-ccfdna/)**

 Topics: [AMP](https://blog.seracare.com/ngs/tag/amp), [SeraSeq](https://blog.seracare.com/ngs/tag/seraseq), [liquid biopsy](https://blog.seracare.com/ngs/tag/liquid-biopsy), [cfDNA](https://blog.seracare.com/ngs/tag/cfdna), [ctDNA](https://blog.seracare.com/ngs/tag/ctdna)

 

 

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