Insights from Comprehensive Genomic Panel Analysis of CLL in a Low-Prevalence (Mexican) Population

Melania Abreu González, MD/MS
Clinical Geneticist & Co-Founder, Genos Médica (Mexico)

Chronic lymphocytic leukemia (CLL) is the most common leukemia in adults across Western countries, but its incidence in Latin America is 3–5× lower, with some of the lowest rates observed in regions with high Amerindian ancestry. In Mexico, CLL represents only 7% of leukemia cases in Mestizo populations, making comprehensive molecular insights rare and highly valuable.

In this focused on-demand session, Dr. Abreu shares new learnings from targeted NGS analysis in the low-prevalence Mexican population and discusses how modern tools can reshape CLL assessment, stratification, and accelerate decision-making.

What You’ll Learn

CLL’s molecular and clinical heterogeneity
Why predicting outcomes remains challenging and how genetic alterations shape prognosis and therapy.
The value of NGS for CLL analysis
Consolidated detection of SNVs, Indels, CNVs, and IGHV status; improved visibility of clonal populations; and enhanced cost efficiency with batch processing; seamless integration with IgCaller for immunoglobulin rearrangement characterization.
Practical workflow advantages
How a single, scalable NGS application can:
– Improve efficiency
– Support earlier risk stratification
– Maintain high-quality variant characterization while reducing overall costs

Why Watch?

Get clear, real-world guidance on optimizing CLL workflows and generating meaningful insights in populations where data is limited.

Watch Webinar

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