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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 a new method for estimating genetic variant effects on transcription factor regulatory events, integrating diverse omics data to build interpretable regulatory networks for disease insights.
Explore how somatic mutations in brain development contribute to neurodevelopmental disorders using integrated single-cell and long-read RNA sequencing techniques.
Explore cell type-specific vulnerability in traumatic brain injury, focusing on hippocampal damage and its impact on neural stem cells and cognitive impairment.
Explore long-read sequencing's revolutionary impact on human genetics, enabling rapid genome assembly and comprehensive variation detection for enhanced disease understanding.
Explore innovative gene therapy solutions, focusing on AAV plasmid DNA sequencing and synthesis for rAAV production, including ITR region management in clinical development.
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.
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