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Explore a novel saliva-based RT-PCR assay for SARS-CoV-2 detection, featuring simplified sample processing and high sensitivity, presented by an experienced molecular biologist.
Explore recent advances in lyophilized qPCR reagents for molecular diagnostics, focusing on rapid results, performance, and quality. Learn about applications in infectious diseases, genetic testing, and oncology.
Discover automated NGS library prep solutions to streamline workflows, reduce labor, and overcome adoption challenges. Learn about the AVENIO Edge System for efficient genomic research.
Discover Thermo Fisher's innovative approach to accelerate antibody and protein therapeutics development, from gene optimization to first-in-human trials, through an integrated workflow.
Explore high-throughput Luminex assays for multiplex gene and protein analysis, featuring ProcartaPlex and QuantiGene Plex technologies. Learn automation strategies for increased efficiency in genomic and proteomic research.
Explore high-throughput DESI-MS for drug discovery, including reaction screening, nano-scale synthesis, and bioanalysis. Learn innovative techniques for faster compound library synthesis and bioactivity assessment.
Learn strategies for developing effective saliva-based lateral flow immunoassays, addressing challenges like matrix effects and sample variability to create successful point-of-care and over-the-counter tests.
Explore LC-MS workflows for infectious disease detection, including SARS-CoV-2 monitoring. Learn about peptide enrichment, immunoprecipitation, and protein precipitation techniques for improved disease surveillance.
Explore a global federated system for biosurveillance using genomic, epidemiological, climate, and environmental data to model biological risks and enhance pandemic early warning capabilities.
Explore AI-driven functional precision medicine for cancer, combining live-cell assays, immune profiling, and machine learning to predict drug efficacy and improve treatment outcomes.
Explore the benefits of combining short read whole genome sequencing, optical genome mapping, and transcriptome analysis for improved constitutional and cancer diagnostics.
Explore a novel long-read sequencing method for detecting single-strand DNA mismatches and damage, enabling new insights into mutation origins in healthy tissues and cancer.
Explore the complex relationship between race, ethnicity, and genetics in medicine. Examine the implications of using racial categories in clinical care and laboratory practices.
Explore the shift from traditional culture methods to PCR in infectious disease diagnostics, focusing on improved speed, accuracy, and patient care implications.
Explore long-read sequencing's advantages in genome analysis, focusing on accuracy improvements for complex genes and large-scale cohort studies in personalized medicine initiatives.
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