
Explore CRISPR/Cas-enabled paper microfluidics for rapid pathogen detection, including SARS-CoV-2 diagnosis and wastewater surveillance. Learn about low-cost, deployable biosensors for public health applications.

Explore CRISPR base and prime editing technologies, their applications, and potential for treating genetic disorders without harmful double-strand breaks. Learn from expert Dr. Cihan Tastan in this cutting-edge webinar.

Explore advanced structural variant detection using Sniffles2, a powerful tool for identifying complex genomic alterations with increased accuracy, speed, and functionality in long-read sequencing data.

Explore metabolic barriers to tumor immunity in pancreatic cancer, focusing on nutrient stress impact and potential strategies to enhance immunotherapy effectiveness.

Explore T cell response generation in immunosuppressive tumor environments, focusing on overcoming challenges in pancreatic cancer and enhancing dendritic cell function for effective immunotherapy.

Explore gene regulatory networks and individual-specific disruptions, focusing on disease-associated genetic variants and their impact on transcription factor binding and gene expression.

Explore high-throughput qPCR microfluidics technology for plant and animal genomics, offering singleplex accuracy, massive parallelization, and efficient screening of multiple pathogens or SNPs.

Explore strategies to minimize off-target edits in gene editing experiments. Learn best practices, considerations for different scenarios, and optimized workflows to enhance precision in genome manipulation.

Enhance microbial detection in human microbiome samples through unbiased host DNA/RNA depletion. Learn about CRISPRclean technology for improved taxonomic resolution and increased microbial genome coverage.

Explore new methods and technologies accelerating sequence-based screening of plasmids for discovery, research, and biotechnology. Learn about ExpressPlex technology and its integration with rolling-circle amplification in OCTOPUS v3.0.

Explore a comprehensive gene-to-protein workflow solution for reliable recombinant protein expression in eukaryotic cells, optimizing yields for structural and functional analyses in biomedical research and drug development.

Explore a novel integrated workflow for efficient CTC enrichment, enumeration, and identification in metastasis research. Learn about unbiased size selection and compatibility with various molecular and cellular applications.

Explore a comprehensive structural variation map of Han Chinese genomes using long-read sequencing, uncovering genetic insights and implications for human evolution and disease.

Explore genome sequencing, from genotype to phenotype, with a focus on telomere length and its implications for aging, disease, and health disparities in minority populations.

Explore sex and gender differences in COPD, focusing on epigenetic findings related to disease susceptibility, severity, and aging. Gain insights from a respiratory epidemiologist on this leading cause of death.

Explore complete human genome assemblies, unlocking insights into complex regions and revolutionizing genetics. Gain new perspectives on genome biology and structure through telomere-to-telomere chromosome analysis.

Explore the groundbreaking assembly of human chromosome 8, unraveling its structure, function, and evolutionary history. Gain insights into centromere evolution and the resolution of long-standing genomic gaps.

Explore epigenetic clocks in mammals, their accuracy across species, and implications for aging research. Gain insights into DNA methylation's role in biological aging and lifespan.

Explore advancements in genomic benchmarking for medically-relevant autosomal genes. Learn about GIAB consortium's efforts to improve variant calling in challenging genomic regions.

Explore mechanisms behind sex differences in disease, focusing on X chromosome factors. Discover non-hormonal origins of sex bias and their impact on disease progression and treatment approaches.

Explore how somatic mutations in brain development contribute to neurodevelopmental disorders using integrated single-cell and long-read RNA sequencing techniques.