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Discover a scalable targeted enrichment protocol for long DNA fragments, demonstrated with a custom blood group panel and highly multiplexed enrichment pool of 16 samples.
Explore mRNA applications and production challenges, focusing on BASE's strategies for optimizing workflows and increasing capabilities using synthetic templates.
Explore advanced NGS solutions for cancer and MRD research, enhancing library complexity and offering customizable hybridization capture approaches.
Explore CRISPR gene editing technology, its applications, and IDT's Alt-R products through an overview of design tools, reagents, and a case study on CRISPR solutions.
Discover high-throughput CRISPR genome editing techniques for research and drug discovery, focusing on arrayed synthetic guide RNA libraries and custom solutions.
Explore advanced techniques for identifying ultra-low frequency variants in cancer research, enhancing biomarker discovery and personalized treatment strategies.
Discover strategies for designing potent antisense oligonucleotides with minimal off-target effects, focusing on gapmer ASOs and their mechanisms for modulating gene expression.
Explore extraction-free PCR for target identification in diverse samples, including urine, saliva, and plant tissues. Learn about IDT's one-step master mix for efficient direct amplification.
Optimize CRISPR genome editing in primary T cells with improved methods for cell culture, delivery, and knock-in rates using HDR donors and enhancing reagents.
Explore efficient and accurate methylation profiling tools for low-input samples with IDT's xGenâ„¢ Methyl-Sequencing Workflow.
Explore AI/ML-guided antibody design for faster, more effective therapeutic discovery using an integrated platform that combines high-speed wet lab with advanced automation.
Explore qPCR reagent tools and PrimeTimeâ„¢ One-Step 4X Broad-Range qPCR Master Mix for amplification from extracted or crude samples. Learn advantages, building blocks, and performance in various conditions.
Explore next-generation sequencing's role in advancing hematology research and personalized genomics for improved patient outcomes.
Explore the evolution and impact of whole exome sequencing at MGI, including applications, read depth, CNV detection, and gene fusion identification.
Explore whole exome sequencing's potential in rare disease research, focusing on case studies and advanced techniques for uncovering genetic causes.
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