Countable Labs’ Events
Booth 943
Stop by to talk with our team about transforming your current PCR assays
Poster Session D
Development of a single-tube, 8-color PCR assay for quantifying a KRAS mutation panel using true single-molecule counting
Track: Screening Applications and Biomarker Diagnostics
Tuesday, February 10 | 2:00 - 3:00 PM ET
Poster 423
"A single-molecule PCR framework bridging low-plex PCR and NGS for biomarker validation at 16-plex and beyond."
Tuesday, February 24 | 1:30–3:30 PM EST
Poster 469
"Quantifying reverse transcription efficiency through single-molecule analysis with Countable PCR for enhanced NGS library preparation optimization."
Tuesday,February 24 | 1:30–3:30 PM EST
Poster 2594
"A deep sampling and single-molecule digital counting assay for rare molecule detection."
Session Category: Clinical Research
Session: Liquid Biopsies: Circulating Nucleic Acids 2
Poster Section 46 — Poster Board Number: 13
Monday, April 20 | 9:00 AM - 12:00 PM PST
Poster 7615
"Multiplex detection of BCR-ABL1 fusion transcripts in a streamlined single-tube workflow using PCR-based single-molecule counting."
Session Category: Prevention / Early Detection / Interception
Session: Cancer and Cancer-Related Alterations, Detection Approaches, andMolecular Characterization
Poster Section 36 — Poster Board Number: 2
Wednesday, April 22 | 9:00 AM - 12:00 PM PST
Booth #1409
May 12-14
Talk
“Rapid, High-Resolution Multiplex Characterization of DNA Impurity Integrity in rAAV Products using Single-Molecule Partitioning"
Dr. David Dobnik | National Institute of Biology, Slovenia
Thursday, May 14 | 8:00 AM EST
Room: MCEC Room 206AB (Level 2)
Poster 1066
"Early vector copy number determination and integration assessment for cell therapy using single-molecule PCR"
Presented in collaboration with Carrigent
Tuesday, May 12| 5:00 PM - 6:30 PM EST
Poster 2218
"Rapid assessment of AAV genome integrity using multiplexed PCR with single-molecule detection"
Presented in collaboration with AAVnerGene
Wednesday, May 13 | 5:00 PM - 6:30 PM EST
June 15-17
Talk and Poster Presentation
“Single-tube multiplex quantification of BCR::ABL1 fusion transcripts enables sensitive MRD monitoring across isoforms in CML/ALL”
Talk AS-03 - Abstract Session 3 - Hematopathology
Dr. Pamela Ward | Molecular Pathology at Keck Medical Center, USC
Date: Wednesday, June 17 I 11:30 AM EEST
Location: Ballroom
Poster H-03
Presented in collaboration with USC
Tuesday, June 16 at 10:20 AM
Location: Poster Exhibition Area
Talk
“Ultra-sensitive, multiplexed cfDNA variant detection at the single-molecule level”
Dr. Eleen Shum | Countable Labs, Inc.
Monday, June 15 | 2:00 - 2:15 PM EEST
Location: Main Exhibition Area
Poster H-06
“Evaluation of a deep-sampling PCR assay for KIT D816V detection at ultra-low variant allele frequencies”
Presented in collaboration with LabCorp
Wednesday, June 17 | 9:00 AM EEST
Location: Poster Exhibition Area
This joint webinar, presented in collaboration with Countable Labs and Promega, walks through a complete workflow from cfDNA extraction using the Promega Maxwell® System followed by ultra-sensitive variant detection using Countable PCR. Using multiplexed KRAS allele detection and BCR-ABL isoform analysis as real-world examples, attendees will learn how pairing quality extraction with single-molecule counting PCR delivers higher sensitivity and reproducibility than qPCR, dPCR, or NGS with a simpler workflow and lower cost per sample.
Key topics that will be covered:
- Sensitivity where it counts: a complete cfDNA workflow for detecting clinically relevant variants down to 0.07% variant allele frequency (VAF) for KRAS G12C
- Reproducibility without the burden: how single-molecule counting PCR eliminates standard curves, Poisson statistics, and reduces replicates, giving labs consistent, confidence-worthy results run-to-run
- Lower cost per sample, simple operations: how automating extraction and consolidating multiple targets into a single tube, all relevant BCR-ABL isoforms in one reaction, or multiple KRAS variants cuts reagent usage and hands-on time without compromising sensitivity
- A complete cfDNA workflow from extraction to result: how pairing automated extraction with single-molecule counting PCR enables a faster and more streamlined high-confidence workflow for variant calls
