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Inside the Coursera-Udemy Deal: Three Bids, Two Years and a Rival Suitor

Buried in Coursera’s 300-page prospectus: two failed merger attempts, competing bidders, a rogue shareholder, and a combined market cap that shrank from $3.8 billion to $1.7 billion.

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Ambry Genetics
Will RNA Testing Be the Next Del-Dup for Clinical Genetics - Webinar - Ambry Genetics

Explore how RNA genetic testing enhances hereditary cancer diagnostics, increasing detection of actionable variants and reducing inconclusive results through concurrent DNA and RNA analysis.
- YouTube
- 1 hour 2 minutes
- Self-Paced
- Free Video
Ambry Genetics
Review Tools of UCSC Genome Browser - Clinical Diagnostic Series - Webinar - Ambry Genetics

Explore UCSC Genome Browser's tools for visualizing and analyzing genomic data through an interactive demo, covering features like data tracks, multi-region browser, and personal genome snips.
- YouTube
- 49 minutes
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- Free Video
Ambry Genetics
Analyzing Historical Mutations in the Cystic Fibrosis Gene - Ambry Genetics

Genetic counselors analyze CFTR gene mutations, discussing reclassified variants and implications for genetic testing in cystic fibrosis and related disorders.
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Ambry Genetics
The Basics of Autism Spectrum Disorders and the Genetic Link - Webinar - Ambry Genetics

Explore autism spectrum disorders, genetic links, inheritance patterns, and diagnostic strategies. Learn about recurrence risks, epigenetics, and the impact of diagnosis from an experienced pediatrician and geneticist.
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Medicosis Perfectionalis
Homocystinemia: Causes, Symptoms, Diagnosis, and Treatment - Biochemistry and Genetics

Explore homocystinemia's causes, symptoms, diagnosis, and treatment. Understand the biochemistry and genetics behind this autosomal recessive condition affecting homocysteine metabolism.
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Medicosis Perfectionalis
Marfan Syndrome vs. Ehlers-Danlos Syndrome - Biochemistry and Genetics

Explore the genetic and biochemical differences between Marfan Syndrome and Ehlers-Danlos Syndrome, focusing on connective tissue defects, symptoms, and clinical manifestations.
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Broad Institute
MPG Primer: A Statistical Genetics Guide to Identifying HLA Alleles Driving Complex Disease - 2023

Explore statistical genetics techniques for identifying HLA alleles associated with complex diseases. Learn about human genetic variation, genotyping, and data analysis methods in population genetics.
- YouTube
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Cardiology University of Washington
Cardiomyopathy Genetics: Current and Evolving Applications

Uncover the genetic foundations of cardiomyopathies, exploring testing methods and their impact on our understanding of heart muscle diseases.
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Houston Methodist DeBakey CV Education
Genetics of Atrial Fibrillation - DeBakey CV Grand Rounds

Explore the genetic factors underlying atrial fibrillation with Dr. Patrick Ellinor. Gain insights into cutting-edge research and its implications for cardiovascular medicine and patient care.
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Animated biology With arpan
Multiple Myeloma: Pathology, Genetics, Treatment, and MGUS - USMLE Guide

Explore multiple myeloma's pathology, genetics, and treatment, including MGUS. Gain insights for USMLE preparation and enhance understanding of this plasma cell malignancy.
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Non-Hodgkin Lymphoma: Pathology, Genetics, Diagnosis, and Treatment

Explore pathology, genetics, diagnosis, and treatment of Non-Hodgkin lymphoma in this comprehensive overview. Gain insights into this complex blood cancer and its management.
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Broad Institute
PheWAS and UKBB in Medical and Population Genetics - 2024 MPG Primer

Explore phenome-wide association studies (PheWAS) and UK Biobank (UKBB) applications in medical and population genetics, focusing on complex trait analysis and large-scale genomic data.
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Multiple Endocrine Neoplasia Syndromes - Types, Clinical Features, and Genetics

Explore MEN syndromes, their clinical features, and genetic aspects. Gain comprehensive insights into MEN 1, MEN 2, and MEN 4 from Harrison's medical reference.
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Medicosis Perfectionalis
Kearns-Sayre Syndrome and Mitochondrial Disease Genetics

Delve into the genetic complexities of Kearns-Sayre Syndrome, exploring mitochondrial DNA inheritance patterns, clinical manifestations like retinal changes and muscle weakness, and related mitochondrial disorders.
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- 10 minutes
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The Aspen Institute
Deep Dive - Genetics and Genomics, Today and Tomorrow

Explore the impact of genomics on medicine, from the Human Genome Project to CRISPR and gene therapy. Experts discuss current applications and future potential of genetic technologies in healthcare.
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