Oncology

Webinar: Maximize Efficiency: Dual DNA and RNA Purification Solution from the Same Sample

Extraction of DNA and RNA from the sample source maximizes the information gained from precious or limited materials, providing an integrated molecular view. It enables researchers to correlate both genomic and transcriptomic data from the cellular matrix, eliminating the problem of sample variability. Omega Bio-tek has developed an innovative nucleic acid extraction methodology (Mag-Bind® DNA/RNA […]

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Webinar:
June 17th 10:00 am EST
Unlocking Urinary cfDNA Insights: A Complete Workflow from Sample Collection to Detection

Circulating free DNA (cfDNA) derived from urine has emerged as a promising biomarker in the field of non-invasive diagnostics, particularly in oncology, nephrology, and other areas of medical research. With advances in next-generation sequencing (NGS) and other molecular techniques, such as droplet digital PCR (ddPCR), the analysis of cfDNA from urine holds the potential to

Webinar:
June 17th 10:00 am EST
Unlocking Urinary cfDNA Insights: A Complete Workflow from Sample Collection to Detection
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Using ddPCR to Detect Rare Variant Alleles in cfDNA Samples on the MagBinder® Fit24 Platform

Carisa Townsend1, Kiranmai Durvasula1, Julie Baggs1, and Travis Butts1 Omega Bio-tek, Inc, Norcross, GA 30071 Introduction Recent advancements and studies have demonstrated the potential of cfDNA as a universal, non-invasive biomarker in cancer prognosis, diagnosis, and prenatal testing. cfDNA are found in low abundance and in a background of contaminating genomic DNA making it a

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The Challenges of cfDNA Purification

Cell-free DNA (cfDNA) has emerged as a revolutionary tool in the realm of molecular diagnostics, offering a non-invasive window into the genetic information of various bodily tissues. As discussed in a previous post, the development of cfDNA technology is a large step forward in detecting and profiling circulating biomarkers to derive clinically relevant information. However,

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What is NGS?

Next-Generation Sequencing (NGS) is a cutting-edge technology used to sequence nucleotides in a DNA or RNA molecule. Unlike Sanger Sequencing, which can sequence only one DNA fragment at a time, NGS allows researchers to sequence multiple DNA fragments in parallel in a single run. This high-throughput approach revolutionizes our ability to decode complex genomes efficiently

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Liquid vs. Solid Biopsy

Revolutionary advancements in medical technologies have armed physicians with state-of-the-art methods for detecting and monitoring cancer.  Two of these methods are liquid and solid biopsies which provide physicians and researchers with integral information about a patient’s condition.  What is a Solid Biopsy? Solid biopsies are the traditional method of analyzing tumors; this typically involves extracting samples of tissue from the tumor using a needle or

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