Transforming Genomic Medicine with Unprecedented Speed, Accuracy, and Accessibility - PanOmiQ Sets a New Standard with ...

A new study shows that long-read sequencing has the potential to improve the rate of diagnosis while reducing the time to diagnosis from years to days -- in a single test and at a much lower cost.

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A national DNA forensics firm is now working to help identify the headless skeleton remains found in Natchez in 2024. The ...

"The ability to replace multiple legacy assays and simultaneously analyze the genome, methylome, epigenome, and transcriptome ...

Call it the science of small, but a trio of University of Florida chemical engineers have developed a lab-on-a-chip process ...

Long read sequencing revealed more genetic information in cases of 42 patients with rare diseases while cutting time and cost of diagnoses.

With 10K genomic data now publicly available, India takes a major leap in genetic research. In today’s 'Knowledge Nugget', ...

Inaugurating the Centre for Advanced Genomics and Precision Medicine at AIIMS - Jammu, the Union minister of state in the ...

Key Findings Enabled by PacBio Technology: Synchronized Multiomic Sequencing: For the first time, a single sequencing run provided simultaneous insights into genome, methylome, epigenome ...

Chennai: Ahead of World Cancer Day, The Indian Institute of Technology (IIT) Madras on Monday launched Bharat cancer genome ...

Madras on Monday launched a first-of-its-kind cancer genome database to help research on the disease in the country.