seminar

QB3/Bakar Labs Webinar: Jennifer Doudna, UC Berkeley. "The Next Decade of CRISPR"

Professor and Nobel laureate Jennifer Doudna needs no introduction. We're beyond excited to host her in our Distinguished Speaker lunchtime series at Bakar Labs. Join us online to learn from a true pioneer what lies ahead in the next decade for CRISPR and its applications. Catch it live; this will not be recorded.

Where & When

Zoom Webinar, livestreamed from Bakar Labs at UC Berkeley
Wednesday, February 22, 2023, 12:00 to 1:00 PM PT

About the Speaker

Dr. Jennifer A. Doudna is the Li Ka Shing Chancellor’s Chair and a Professor in the Departments of Chemistry and of Molecular and Cell Biology at the University of California, Berkeley. Her groundbreaking development of CRISPR-Cas9 as a genome-engineering technology, with collaborator Emmanuelle Charpentier, earned the two the 2020 Nobel Prize in Chemistry and forever changed the course of human and agricultural genomics research.

This powerful technology enables scientists to change DNA — the code of life — with a precision only dreamed of just a few years ago. Labs worldwide have re-directed the course of their research programs to incorporate this new tool, creating a CRISPR revolution with huge implications across biology and medicine.

In addition to her scientific achievements, Doudna is a leader in public discussion of the ethical implications of genome editing for human biology and societies, and advocates for thoughtful approaches to the development of policies around the safe use of CRISPR technology.

Doudna is an investigator with the Howard Hughes Medical Institute, senior investigator at Gladstone Institutes, and the President of the Innovative Genomics Institute. She co-founded and serves on the advisory panel of several companies that use CRISPR technology in unique ways.

She is a member of the National Academy of Sciences, the National Academy of Medicine, the National Academy of Inventors, and the American Academy of Arts and Sciences. Doudna is also a Foreign Member of the Royal Society, a member of the Pontifical Academy of Sciences, and has received numerous other honors including the Breakthrough Prize in Life Sciences (2015), the Japan Prize (2016), Kavli Prize (2018), the LUI Che Woo Welfare Betterment Prize (2019), and the Wolf Prize in Medicine (2020). Doudna’s work led TIME to recognize her as one of the “100 Most Influential People” in 2015 and a runner-up for “Person of the Year” in 2016. She is the co-author of “A Crack in Creation,” a personal account of her research and the societal and ethical implications of gene editing.

QB3 Webinar: Alex Marson, UCSF/Gladstone. "Decoding and Reprogramming Immune Cell Circuits with CRISPR"

The goal of the Marson lab is to understand genetic circuits that control human immune cell function in health and disease. We have begun to identify autoimmunity risk variants that disrupt immune cell circuits, and how pathogenic circuits may be targeted with novel therapeutics. Our lab has developed new tools for CRISPR genome engineering in primary human T cells. We are now pursuing a comprehensive strategy to test how coding and non-coding genetic variation controls functional programs in the immune system. Genome engineered human T cells hold great potential for the next generation of cell-based therapies for cancer, autoimmunity, and infectious diseases.

Where & When

Zoom Webinar
Thursday, January 19, 2023, 1:00 to 2:00 PM PT

About the Speaker

Alex Marson is Director of the Gladstone-UCSF Institute of Genomic Immunology and Professor in the UCSF Department of Medicine, Division of Infectious Diseases. He serves as the scientific director for Human Health at the Innovative Genomics Institute (IGI) and is a member of the Parker Institute for Cancer Immunotherapy and a Chan Zuckerberg Biohub investigator. Work in Dr. Marson’s lab aims to understand the genetic programs controlling human immune cell function in health and disease, with an emphasis on developing and applying CRISPR genome engineering tools to primary immune cells, especially T cells. Combining genomics and gene editing approaches, the lab works to assess the consequences of coding and noncoding genetic variation on immune cell function and autoimmune disease risk and to genetically engineer human immune cells to target cancer, autoimmunity, and infectious diseases.

QB3 Webinar: Ira Mellman, VP Cancer Immunology, Genentech.

Ira Mellman, PhD, is Vice President of Cancer Immunology at Genentech, a world leader in this vital, complex, and exciting field. Join us on Tuesday, January 17 to learn how an understanding of the basic science can inform the quest to discover and develop novel, effective therapies for cancer. Dr. Mellman will speak on where cancer immunotherapy is, where it is going, and what the opportunities are.

Where & When

Zoom Webinar (streamed live from Bakar Labs)
Tuesday, January 17, 2023, Noon to 1:00 PM PT

About the Speaker

Ira Mellman came to Genentech in the Spring of 2007 as Vice President of Research Oncology, after more than 20 years as a faculty member at the Yale University School of Medicine, where he was chair of his department (Cell Biology), a member of the Ludwig Institute for Cancer Research, scientific director of the Yale Cancer Center, and Sterling Professor of Cell Biology and Immunobiology. Dr. Mellman has a BA from Oberlin College & Conservatory and a PhD in Genetics from Yale. He was a Postdoctoral Fellow at the Rockefeller University with Ralph Steinman, who received the Nobel Prize for the discovery of dendritic cells. His laboratory is known not only for advances in fundamental cell biology particularly in the area of membrane traffic (including the discovery of “endosomes”) but also for applying these insights to understanding the cellular basis of the immune response, especially dendritic cell function. He was also the founder of CGI Pharma, which was recently purchased by Gilead. Ira ran all of oncology research at Genentech until the end of 2013 when he decided to concentrate his efforts on the rapidly developing area of cancer immunotherapy and became Vice President of Cancer Immunology. Ira is a member of the National Academy of Sciences, American Academy of Arts & Sciences, the European Molecular Biology Organization, and the former Editor in Chief of the Journal of Cell Biology. He has also served on the editorial boards of Cell, the Journal of Experimental Medicine, EMBO Journal, among others. He also serves on the boards of the Society for the Immunotherapy of Cancer, the American Society for Cell Biology, and the Cancer Research Institute. He remains a frustrated composer and songwriter, and has recorded two CDs in the little-known genre of “bio-rock”.

QB3 Webinar: Ben Cravatt, Scripps Research. "Activity-Based Proteomics: Target and Ligand Discovery on a Global Scale"

Advances in DNA sequencing have radically accelerated our understanding of the genetic basis of human disease. However, many of human genes encode proteins that remain uncharacterized and lack selective small-molecule probes. The functional annotation of these proteins should enrich our knowledge of the biochemical pathways that support human physiology and disease, as well as lead to the discovery of new therapeutic targets. To address these problems, we have introduced chemical proteomic technologies that globally profile the functional state of proteins in native biological systems. Prominent among these methods is activity-based protein profiling (ABPP), which utilizes chemical probes to map the activity state of large numbers of proteins in parallel. In this lecture, I will describe the application of ABPP to discover and functionally annotate proteins that contribute to human diseases, such as cancer and autoimmunity. I will also discuss the generation and implementation of advanced ABPP platforms for proteome-wide ligand discovery and how the integration of these global ‘ligandability’ maps with emergent human genetic information and phenotypic screening can expand the druggable fraction of the human proteome for basic and translational research objectives.

Where & When

Zoom Webinar
Monday, December 12, 2022, 1:00 to 2:00 PM PT
(Rescheduled from earlier date)

About the Speaker

Dr. Cravatt is Professor and Norton B. Gilula Chair of Chemical Biology in the Department of Chemistry at The Scripps Research Institute. His research group is interested in developing chemical proteomic technologies that enable protein and drug discovery on a global scale and applying these methods to characterize biochemical pathways that play important roles in human physiology and disease. Dr. Cravatt obtained his undergraduate education at Stanford University, receiving a B.S. in the Biological Sciences and a B.A. in History. He then received a Ph.D. from The Scripps Research Institute (TSRI) in 1996. Professor Cravatt joined the faculty at TSRI in 1997. Dr. Cravatt’s honors include a Searle Scholar Award, the Eli Lilly Award in Biological Chemistry, a Cope Scholar Award, the ASBMB Merck Award, the RSC Jeremy Knowles Award, the AACR Award for Achievement in Chemistry in Cancer Research, the Wolf Prize in Chemistry, and memberships in the National Academies of Medicine and Sciences.

QB3 Webinar: Chris Mason, Weill Cornell: "Functional Genomics, Space Travel, and the Survival of the Human Species"

The Mason laboratory is working on a ten-phase, 500-year plan for the survival of the human species on Earth, in space, and on other planets. To that end, we develop and deploy new biochemical and computational methods in functional genomics to elucidate the genetic basis of human disease and human physiology. We focus on novel techniques in next-generation sequencing and algorithms for tumor evolution, genome evolution, DNA and RNA modifications, and genome/epigenome engineering. We work closely with NIST/FDA to build international standards for these methods and ensure clinical-quality genome measurements and editing. We also collaborate with NASA to build integrated molecular portraits of genomes, epigenomes, transcriptomes, and metagenomes for astronauts, which help establish molecular foundations and genetic defenses for long-term human space travel.

Where & When

Zoom Webinar
Tuesday, December 6, 2022, 1:00 to 2:00 PM PT

About the Speaker

Dr. Christopher Mason completed his dual B.S. in Genetics and Biochemistry (2001) from University of Wisconsin-Madison, his Ph.D. in Genetics (2006) from Yale University, and then completed post-doctoral training in clinical genetics (2009) at Yale Medical School while jointly a post-doctoral Fellow of Genomics, Ethics, and Law at Yale Law School (2009). He is currently an Associate Professor at Weill Cornell Medicine, with appointments at the Tri-Institutional Program in Computational Biology and Medicine between Cornell, Memorial Sloan-Kettering Cancer Center and Rockefeller University, the Sandra and Edward Meyer Cancer Center, and the Feil Family Brain and Mind Research Institute.

QB3 & Berkeley Law Panel: "What Your IP Attorney Wishes You'd Known Before Starting Your Company"

You've identified an unmet need in the life sciences or healthcare space, and developed a clever solution. You're ready to move forward in commercializing your solution into a product, but you will need funding and partnerships to succeed. How can you set yourself up for success--in particular, what do you need to know about your IP landscape and protection strategy, before meeting with potential partners and funders? Join our November 17 webinar featuring WSGR attorney Ali Alemozafar in spirited conversation with serial entrepreneurs Uri Lopatin and Greg Went and investors Neena Kadaba and Maria Fardis. Bring your own questions! Hosted in conjunction with the Berkeley Center for Law and Technology's Life Sciences Project.

Where & When

Zoom Webinar
Thursday, November 17, 2022, 1:00 to 2:00 PM PT

About the Speakers

Ali R. Alemozafar, PhD is a partner at Wilson Sonsini Goodrich & Rosati, where he focuses on strategic intellectual property counseling in a wide range of technical fields, including diagnostics, tools, genomics, digital health, bioinformatics, artificial intelligence, materials and various engineering fields. His expertise includes patent strategy, patent prosecution, and patent diligence—including freedom-to-operate analyses—for financings, mergers and acquisitions, and public offerings. Ali has prepared and prosecuted patent applications in the United States and other jurisdictions, including Europe, China, and Japan. He provides legal counseling to companies at various stages of growth, from pre-financing start-ups to public companies.

Prior to joining the firm, Ali worked on data warehousing, business intelligence, and enterprise data integration. He frequently lectures at the UC Berkeley School of Law and UC Hastings College of the Law on various intellectual property topics, including patent strategy and IP due diligence.

Maria Fardis, PhD joined the Frazier Life Sciences team as a Venture Partner in 2021. She has over 20 years of scientific and management experience in numerous public and private companies. She is also the Chief Executive Officer of 4PinesCo, Inc., a Frazier-founded search company focused on identifying, in-licensing, and developing high-quality therapeutic candidates.

Maria previously served as President and Chief Executive Officer of Iovance Biotherapeutics. She transformed Iovance from an early-stage development company to a company with multiple late-stage programs involving lifileucel and LN-145 for the treatment of multiple solid tumors. She raised over a billion dollars in multiple rounds of financing for the company. Prior to Iovance, Maria served as the Chief Operating Officer of Acerta Pharma B.V., where she worked on the development of Calquence® until the company’s acquisition by AstraZeneca. Prior to that, she worked at Pharmacyclics, Inc., where she was a key contributor in the creation of a broad clinical program leading to global approvals for Imbruvica® in multiple hematologic malignancies, and where she served as Chief of Oncology Operations and Alliances. Prior to joining Pharmacyclics, Maria held increasingly senior positions in Medicinal Chemistry and the project and portfolio management department at Gilead Sciences, Inc., where she was involved with multiple therapeutic areas including antivirals, oncology, and cardiovascular therapeutics and worked on the development and life cycle management of Letairis®.

Maria received her Ph.D. in Organic Chemistry from the University of California, Berkeley and her B.S. summa cum laude, in chemistry from the University of Illinois, Urbana-Champaign. She also holds an M.B.A., received with highest honors, from Golden Gate University.

Neena Kadaba, PhD, an entrepreneur in residence at ATP, is a science-driven investor with 15 years of experience building novel collaborations and partnerships to drive innovation. Most recently, Neena was a Director at Quark Venture, where she served on the board of Eyevensys, IOME BIO, Calcimedica, and EyeYon on behalf of the Global Health Sciences Fund and led diligence for a number of additional investments. Previously, she was the Director of Strategic Partnerships at QB3, an institute at the University of California, where she created new programs to accelerate startups and worked with QB3's venture fund, Mission Bay Capital. Prior to QB3, Neena was a Kauffman Fellow while she was an Associate in Venture Investment at Itochu Technology, Inc, the California office of Itochu, the Japanese trading company, and she began her career in venture at California Technology Ventures.

Neena received her PhD in chemistry from the California Institute of Technology (Caltech), where she solved the structure of a novel membrane protein using x-ray crystallography and protein structure modeling. She received her undergraduate and masters’ degrees from the Massachusetts Institute of Technology (MIT) in chemistry and bioengineering, respectively.

Uri Lopatin, MD is a biotech entrepreneur and has worked in various executive clinical and translational science positions for esteemed organizations, including Schering Plough, Roche, Gilead Sciences, and Y Combinator where he served as a visiting partner. He also co-founded Assembly Pharmaceuticals, functioning as both Chief Medical Officer and Vice President of Research, and successfully raising over $300 million to move two first-generations of novel therapeutics for hepatitis B into global Phase 1 and Phase 2 clinical studies. Uri has published and patented broadly in virology and immunology.

Uri received a BA in Biology from Cornell University and MD degree at the University of Medicine and Dentistry of New Jersey – New Jersey Medical School. He completed his residency at New York University Medical Center, internship at the University of Washington, and fellowship training in Infectious Disease at the National Institutes of Health.

Greg Went, PhD is CEO of Reflexion Pharmaceuticals. Greg is an experienced entrepreneur with multiple successful startups in the life sciences, including genomics, genetics, diagnostics and therapeutics companies. These companies have taken multiple products from idea through approval and commercialization, benefiting the lives of patients and care partners.

Greg founded Adamas Pharmaceuticals and guided the company’s growth as CEO and Chairman from inception to September 2019, when he became a strategic advisor to the company. He developed the original technology platform, based upon the understanding and modelling of time-dependent biological phenomena. He steered Adamas through the licensing of assets related to Namenda XR and Namzaric to Forest Laboratories (now Allergan), the company’s IPO, and commercial preparation for the potential launch of a new medicine for patients with Parkinson’s disease.

Prior to Adamas, Greg co-founded CuraGen Corporation in 1992, one of the first genomics companies, where he served as Executive Vice President and Director. Greg has served on the board of directors of Angelica, Parallele Biosciences and Tethys Biosciences.

Greg has published in the fields of catalysis, spectroscopy, DNA sequencing, gene expression profiling, neuroscience, influenza and neurology. He is an inventor on over 70 issued and pending patents. He received his Ph.D. in Chemical Engineering from the University of California, Berkeley, his B.S. in Chemical Engineering from Carnegie Mellon University, and did additional post-doctoral work at Cornell University.

QB3 Meeting, Sara Fröjdö, FIND. "How FIND Can Help Identify Diagnostic Gaps and Support Your Market Access in Low- and Middle-Income Countries"

This is now a meeting (not a webinar). If you register, we will send you the link.

COVID has highlighted the essential role of diagnostics as an enabler of access to health and the linchpin of early warning and response systems for health emergencies. The number of, and investment in, new technological approaches has dramatically accelerated. However, the pandemic has also exposed significant diagnostic gaps, notably in low- and middle-income countries (LMICs), in areas such as diagnostics literacy, funding, regulatory pathways, stakeholder engagement and evidence generation. FIND, the global alliance for diagnostics, seeks to fill these gaps and ensure equitable access to reliable diagnosis. Join our Nov 17 webinar with Sara Fröjdö, Senior Technology Officer at FIND, to learn how her organization connects countries and communities, funders, decision-makers, healthcare providers and developers to spur diagnostic innovation and make testing an integral part of sustainable, resilient health systems.

Where & When

Zoom Meeting
Wednesday, November 2, 2022, 1:00 to 2:00 PM PT

About the Speaker

Sara Fröjdö joined FIND in 2022 as Senior Technology Officer, Business Intelligence, with the key role of supporting the organization in identification and assessment of new opportunities, selection of partners and initiation of collaborations.

Prior to joining FIND, Sara spent 10 years in innovation and new market development consulting working with start-ups, biotechnology companies and leading healthcare industrials followed by partnership and business development in the field of diagnostics for a technology research institute.

She received her PhD in Biochemistry and Molecular Biology from the University of Lyon and her MSc in Biology from the University of Helsinki.

QB3 Webinar: Carolyn Bertozzi, Stanford. "Therapeutic Opportunities in Glycoscience"

Congratulations to Prof. Bertozzi on winning the 2022 Nobel Prize in Chemistry!

Cell surface glycans constitute a rich biomolecular dataset that drives both normal and pathological processes. Their “readers” are glycan-binding receptors that can engage in cell-cell interactions and cell signaling. Our research focuses on mechanistic studies of glycan/receptor biology and applications of this knowledge to new therapeutic strategies. Our recent efforts center on pathogenic glycans in the tumor microenvironment and new therapeutic modalities based on the concept of targeted degradation.

Where & When

Zoom Webinar
Wednesday, October 19, 2022, 1:00 to 2:00 PM PT

About the Speaker

Carolyn Bertozzi is the Baker Family Director of Stanford ChEM-H and the Anne T. and Robert M. Bass Professor of Humanities and Sciences in the Department of Chemistry at Stanford University. She is also an Investigator of the Howard Hughes Medical Institute. Her research focuses on profiling changes in cell surface glycosylation associated with cancer, inflammation and infection, and exploiting this information for development of diagnostic and therapeutic approaches, most recently in the area of immuno-oncology. She is an elected member of the National Academy of Medicine, the National Academy of Sciences, and the American Academy of Arts and Sciences. She also has been awarded the Lemelson-MIT Prize, a MacArthur Foundation Fellowship, the Chemistry for the Future Solvay Prize, among many others.

QB3 Webinar: Howard Chang, Stanford. "Personal Regulome Navigation of Cancer"

Cancer is a disease of genes. Yet the elucidation of cancer genomes does not mean we have conquered cancer; the central challenge is in their interpretation. In every human cell, two meters of DNA is packed into a ~10 micron nucleus. The genome is extensively compacted, except for the active regulatory DNA elements that remain accessible. I will describe new technologies based on DNA transposition that reveal the epigenomic profiles of single cells or from clinical biopsies of disease states. The landscape of active DNA regulatory elements are further linked to 3D genome architecture, mutational profiles, and RNA output to reveal the targets of disease associated DNA elements, such as inherited genetic variants or those modified by environmental stimuli. Our analysis of 23 human cancer types reveal nearly half a million active DNA elements across human cancers, disclose oncogenic extrachromosomal DNA, and identify gene-regulatory interactions underlying cancer immune evasion. These results suggest a systematic approach to understanding the noncoding genome in cancer to advance diagnosis and therapy. 

Where & When

Zoom Webinar
Thursday, September 22, 2022, 1:00 to 2:00 PM PT

About the Speaker

Howard Y. Chang M.D., Ph.D. is Director of the Center for Personal Dynamic Regulomes and the Virginia and D.K. Ludwig Professor of Cancer Research at Stanford University. He is a Howard Hughes Medical Institute Investigator; he is also Professor of Dermatology and of Genetics at Stanford University School of Medicine. Chang earned a Ph.D. in Biology from MIT, M.D. from Harvard Medical School, and completed Dermatology residency and postdoctoral training at Stanford University. His research addresses how large sets of genes are turned on or off together, which is important in normal development, cancer, and aging. Chang discovered a new class of genes, termed long noncoding RNAs, can control gene activity throughout the genome, illuminating a new layer of biological regulation. He invented ATAC-seq and other new methods for defining DNA regulatory elements genome-wide and in single cells. The long term goal of his research is to decipher the regulatory information in the genome to benefit human health.

Dr. Chang is a Member of the National Academy of Sciences, National Academy of Medicine, and American Academy for the Arts and Sciences. Dr. Chang’s honors include the NAS Award for Molecular Biology, Outstanding Investigator Award of the National Cancer Institute, Paul Marks Prize for Cancer Research, Judson Daland Prize of the American Philosophical Society, and the Vilcek Prize for Creative Promise. His work was honored by the journal Cell as a Landmark paper over the last 40 years and by Science as “Insight of the decade”.

QB3 Webinar: Elvis Chan, FBI, Allison Henry, UC Berkeley, & Pat Phelan, UCSF. "Cybersecurity: What You Need to Know in 2022"

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Cybersecurity is a key issue for us in our private lives — think identity theft — and at the national scale — such as federal elections. For scientists in academic & commercial labs, threats include IP theft, ransomware, and hacktivism. Where are we vulnerable to those who want to disrupt or steal from us? How can we do the best possible job of protecting ourselves and the organizations we serve? Join us to learn best practices from the FBI's Elvis Chan, who manages San Francisco’s Cyber Branch, which is responsible for cyber investigations and digital forensics, and Allison Henry and Patrick Phelan, chief information security officers at UC Berkeley and UCSF respectively.

Co-sponsored by the UCSF Cyber-Champion Team.

Where & When

Zoom Webinar
1:00 to 2:00 PM, Tuesday, May 17, 2022

About the Speakers

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Elvis Chan is an Assistant Special Agent in Charge (ASAC) assigned to FBI San Francisco. ASAC Chan manages the field office’s Cyber Branch, which is responsible for cyber investigations, digital forensics, technical operations, and private sector engagement. With over 15 years in the Bureau, he is a decorated agent who is recognized within the Intelligence Community as an election cybersecurity and cyberterrorism expert. ASAC Chan was the lead agent on significant cyber investigations and managed joint counterterrorism operations with domestic and foreign law enforcement agencies. Prior to joining the Bureau, ASAC Chan was a process development engineer in the semiconductor industry for 12 years. He holds two U.S. patents, presents at many technical and law enforcement symposiums, and published multiple articles in journals. SSA Chan graduated from the University of Washington with degrees in chemical engineering and chemistry.


Allison Henry is chief information security officer at UC Berkeley. She wrote her first computer program in BASIC to automate the painfully repetitive task of alphabetizing her weekly 4th grade spelling list. From an early age, she has been building and securing information technology solutions to solve problems and enable people to do what they do best.

After graduating from UC Berkeley with a Bachelor of Science in Integrative Biology in 1996, Allison started her Information Technology career as a system administrator at UC Santa Cruz.

Allison came to UC Berkeley in 2004 when she joined Communications and Network Services and pivoted to Information Security in 2006. In 2013 she started managing the Security Operations team, providing monitoring and incident management services for the complex and heterogeneous UC Berkeley campus computing environment. In that role she led initiatives to modernize security operations through custom built systems for automated alert processing and incident management. This allowed the Security Operations team to scale with the growth of the campus network. In 2018 Allison served as Associate CISO and provided oversight and direction for Information Security Assessments and Compliance activities, before assuming the role of Chief Information Security Officer in December of 2019.

In addition to information technology and security, Allison has a passion for the study of optimizing human performance through fitness and nutrition, and enjoys endurance athletics including trail running and triathlon.


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Patrick Phelan is chief information security officer of UCSF, one of the premier academic medical centers in the country. He is responsible for the security strategy for systems supporting the research, education, and clinical missions of the institution. A 20-year IT veteran, he is a member of several professional organizations, holds CISSP, CEH, CISM certifications, and a B.S. in computer science from UCLA.

QB3 Webinar: Michelle Arkin, UCSF. "Modulating Output of Protein Networks by Targeting Protein-Protein Interactions"

Michelle Arkin chairs the Department of Pharmaceutical Chemistry at UC San Francisco. Her research focuses on the development of drug-like molecules that alter important biological processes. These biological processes often involve complex networks of proteins that interact directly with each other; yet protein-protein interactions are difficult to target with conventional small molecules. Join us for on a briefing on the latest results from her lab.

Where & When

Zoom Webinar
Thursday, May 5, 2022, 1:00 to 2:00 PM PT

About the Speaker

Michelle Arkin’s lab develops innovative approaches to screen for chemical tools and drug leads, using biophysical approaches like fragment-based drug discovery and biological approaches including high-content imaging. Their goal is to demonstrate ‘druggability’ of new target classes and to use their compounds to discover new targets for drug discovery. Areas of interest include protein-protein interactions, allosteric and scaffolding sites in enzymes, focusing on diseases of aging like cancer and neurodegeneration. Michelle is Co-Director of the UCSF Small Molecule Discovery Center, a collaborative research and core lab that includes a high-throughput screening facility and medicinal chemistry. She is co-founder of Elgia Therapeutics and Ambagon Therapeutics.

QB3 Webinar: Anshul Kundaje, Stanford. "Deep Learning for Genomic Discovery"

The human genome contains the fundamental code that defines the identity and function of all the cell types and tissues in the human body. Genes are functional sequence units that encode for proteins. But they account for just about 2% of the 3 billion long human genome sequence. What does the rest of the genome encode? How is gene activity controlled in each cell type? Where do the regulatory control elements lie and what is their sequence composition? How do variants and mutations in the genome sequence affect cellular function and disease?

These are fundamental questions that remain largely unanswered. The regulatory code that controls gene activity is encoded in the DNA sequence of millions of cell type specific regulatory DNA elements in the form of functional DNA words and grammars. This regulatory code has remained largely elusive despite tremendous developments in experimental techniques to profile molecular properties of regulatory DNA.

Deep learning has revolutionized our understanding of natural language, speech and vision. We strongly believe it has the potential to revolutionize our understanding of the regulatory language of the genome. We have developed deep learning frameworks to learn how genomic sequence encodes millions of experimentally measured regulatory genomic events across 100s of cell types and tissues. We have developed novel methods to interpret our models and extract local and global predictive patterns revealing many insights into the syntax and grammar of the regulatory code.

Our models also serve as in-silico oracles to predict the effects of natural and disease-associated genetic variation i.e. how differences in DNA sequence across healthy and diseased individuals are likely to affect molecular mechanisms associated with common and rare diseases. These models enable optimized design of genome perturbation approaches to decipher functional properties of DNA and variants and serve as a powerful lens for genomic discovery.

Where & When

Zoom Webinar
Tuesday, April 5, 2022, 1:00 to 2:00 PM PT

About the Speaker

Anshul Kundaje is an Assistant Professor of Genetics and Computer Science at Stanford University. His primary research area is large-scale computational regulatory genomics. The Kundaje lab specializes in developing statistical and machine learning methods for large-scale integrative analysis of heterogeneous, high-throughput functional genomic and genetic data to decipher regulatory elements and long-range regulatory interactions, learn predictive regulatory network models across individuals, cell-types and species and improve detection and interpretation of natural and disease-associated genetic variation. Previously as a postdoc at Stanford and Research Scientist at MIT, Anshul was the lead computational analyst of the ENCODE Project and the Roadmap Epigenomics Project. Anshul is also a recipient of the 2016 NIH Director's New Innovator Award and the 2014 Alfred Sloan Fellowship.

QB3 Webinar: David Winter, Department of Health & Human Services. "How to work with BARDA and the Division of Research, Innovation, and Ventures"

Dr. Winter’s slide deck is available here.

Where & When

Zoom Webinar
1:00 to 2:00 PM PT, Tuesday, March 22, 2022

About the Speaker

Dr. David Winter is the Team Leader for both the BARDA Accelerator Network and the Blue Knight collaboration with JNJ Jabs. He earned his PhD in immunology/microbiology at SUNY-Buffalo. Before coming to BARDA, he spent 18 years at the bench at Roswell Park Cancer Institute, Johns Hopkins University, NIH, and the Walter Reed Army Institute of Research before moving into Program Management at NIAID/NIH. Dr. Winter left NIH to serve as the external collaborations manager for Novartis Vaccines and Diagnostics in Siena, Italy. In 2010, he returned to NIH and joined the Center for Scientific Review, running two study sections- the Cellular and Molecular Immunology A (CMI-A) study section and the Innovative Immunology SBIR/STTR special emphasis panel. In 2016, he was appointed as an Embassy Science Fellow for the State Department to work with the Indonesian National Academies of Science to design a national peer review system for science grants. Outside of work, Dr. Winter teaches martial arts and races dragon boats.

QB3 Webinar: Caleb Bates, Fish & Richardson. "Unique Challenges of Intellectual Property in the Small Molecule Space"

Every entrepreneur in drug discovery and development knows--or ought to know--that IP is your single most important asset. You need a firm understanding of the patents you control as well as any threats you face from competing claims or unclaimed territory. Companies in the small molecule space face particular challenges including the timing and scope of early patent filings. What's your IP position? Would you like a better understanding of the issues? On Tuesday, March 8, Caleb Bates, J.D., Ph.D. of Fish & Richardson will review key topics in small molecule IP. Join us.

Where & When

Zoom Webinar
Tuesday, March 8, 2022, 1:00 to 2:00 PM

Dr. Caleb Bates is a principal in Fish & Richardson’s Silicon Valley office. His practice focuses on intellectual property law, with emphasis on patent prosecution, strategic counseling, and worldwide patent portfolio management in the pharmaceutical and biotechnology fields. Caleb advises and counsels diverse clients, including early stage and established companies, research institutions, and venture capital and investment firms on how to best develop and leverage their IP assets. In addition to advising clients on IP strategy, Caleb has counseled clients in licensing, investor and company side due diligence, freedom-to-operate and patentability analyses, and in market clearance.

QB3 Webinar: Chris Garcia, Stanford. "Natural and Engineered Cell Surface Receptor-Ligand Interactions in Human Health and Disease"

Christopher Garcia is interested in cell surface receptors and their ligands. Using a range of methodologies, Garcia and his team investigate how ligand recognition and signaling coordinate with the physiology of the cell to determine cell function and fate. In addition to understanding basic aspects of receptor signaling and structural biology, the team is also interested in the creation of novel receptor ligands using protein engineering, and “deorphanization,” or matching of newly discovered receptors to their ligands, using proteomics. A major aim of their work is to synthetically leverage natural biological signaling mechanisms as a path to potential therapeutics.

Where & When

Zoom Webinar
1:00 to 2:00 PM PT, Wednesday, February 23, 2022

About the Speaker

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K. Christopher Garcia, Ph.D. is a Professor of Molecular and Cellular Physiology, and of Structural Biology at the Stanford University School of Medicine. He received his B.S. in Biochemistry from Tulane University, and his Ph.D in Biophysics from Johns Hopkins University. After two years of post-doctoral work at Genentech, Inc. under Dr. David Goeddel in the Dept. of Molecular Biology, where he learned the emerging technologies of protein engineering and recombinant protein expression, Dr. Garcia moved to a second post-doctoral fellowship at The Scripps Research Institute in the laboratory of Prof. Ian Wilson, where he succeeded in determining the first crystal structures of the T cell receptor and then its complex with peptide-MHC. In 1999, Dr. Garcia started his lab at Stanford University School of Medicine in 1999 where he also became an Investigator in the Howard Hughes Medical Institute. Dr. Garcia was elected to the National Academy of Sciences in 2012, and the National Academy of Medicine in 2016.

Dr. Garcia’s interests reside at the cell surface, and his laboratory is investigating structural and functional aspects of cell surface receptor recognition and activation, in receptor-ligand systems with relevance to human health and disease. A common theme is that structural information on receptor-ligand complexes is used to engineer variant proteins and/or surrogates to manipulate receptor signaling and cellular function, as well as act as biological probes to perturb systems in vivo, with an eye towards therapeutic applications. The receptor systems studied derive principally from the immune system (TCR/MHC, cytokines, chemokine GPCR), but additionally encompass several systems that are also important in neurobiology (Neurotrophins, Semaphorins) and development (Notch, Wnt). A focus is on "shared" pleiotropic receptors, to understand the biophysical basis by which different ligands are able to elicit unique intracellular responses and functional outcomes. Dr Garcia’s lab also has an active program in deorphanizing cell surface receptors, including IgSF members. Dr. Garcia has founded or co-founded several biotech companies that are attempting to clinically develop technologies from his lab, including ALXO (SIRP/CD7 antagonist), Synthekine (cytokine engineering), Surrozen (Wnt agonists), 3T (TCR antigen discovery), and Mozart (immune modulation by regulatory T cells).

QB3 Webinar: Aviv Regev, Genentech and Roche. "Cell Atlases as Roadmaps in Health and Disease"

The recent advent of methods for high-throughput single-cell and spatial profiling has opened the way to create a human cell atlas: comprehensive reference maps of all human cells as a basis for both understanding human health and diagnosing, monitoring, and treating disease. Such maps reveal rich biology to help us understand in which cells disease genes act, which cells are disrupted in disease, what mechanisms underlie their (dys)regulation, and what impact therapies would have. In this talk, Aviv Regev, head of Genentech Research and Early Development, will describe how atlases illuminate the relation between genotype to phenotype, especially in the context of human genetics and diseases such as cancer and COVID-19, using single cell genomics as a conceptual and technical framework. She will also describe how this deeper approach to directly probing human biology, in combination with new computational algorithms and new therapeutic modalities, is poised to accelerate the drug discovery process.

Where & When

Zoom Webinar
1:00 to 2:00 PM PT, Wednesday, February 9, 2022

About the Speaker

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As Executive Vice President, Genentech Research and Early Development (gRED), Aviv Regev is responsible for the management of all aspects of Genentech’s drug discovery and drug development activities. She is a member of the Genentech Executive Committee and the expanded Corporate Executive Committee for Roche.

Prior to Genentech, Regev served as Chair of the Faculty, Core Institute Member, founding director of the Klarman Cell Observatory, and member of the Executive Leadership Team of the Broad Institute of MIT and Harvard, as well as Professor of Biology at MIT and Investigator at the Howard Hughes Medical Institute. She is a founding co-chair of the Human Cell Atlas.

Regev has served on multiple corporate advisory, scientific advisory, and journal editorial boards, including the advisory committee to the National Human Genome Research Institute at the National Institutes of Health.

Regev is a leader in deciphering molecular circuits that govern cells, tissues and organs in health and their malfunction in disease. Her lab has pioneered foundational experimental and computational methods in single-cell genomics, working toward greater understanding of the function of cells and tissues in health and disease, including autoimmune disease, inflammation and cancer. She is a member of the National Academy of Sciences and National Academy of Medicine, and she is also a Fellow of the International Society of Computational Biology.

Regev has a Ph.D. in computational biology and a Master of Science from Tel Aviv University.

QB3 Webinar: Kelly Harkins Kincaid, Astrea Forensics. "Cold Case Files: How Astrea Forensics Empowers Law Enforcement"

Forensic genealogy is the art of identifying victims or perpetrators by tracing family connections derived from DNA evidence left at the crime scene. But it's not easy; many detectives solving cold cases must work with fragments of human remains decades old that may fail traditional forensic testing. How can you extract and sequence DNA from a rootless hair or a heavily degraded sample? Astrea Forensics, spun out of Ed Green's lab at UC Santa Cruz, can help, using techniques derived from paleogenetics. In this talk, Astrea CEO and co-founder Kelly Harkins Kincaid will explain how her company empowers law enforcement to bring closure to families of victims who once would have remained anonymous using samples long thought to contain no DNA.

Where & When

Zoom Webinar
Thursday, December 9, 2021, 1:00 to 2:00 PM PT

About the Speaker

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Kelly Harkins Kincaid has BA, MA, and PhD degrees in anthropology and is currently running two genetics companies: Claret Bioscience and Astrea Forensics. As the PI and CEO, she is involved with the design, validation, and commercialization of NGS tools, whether for application in research and the clinic (ClaretBio), or in law enforcement contexts (Astrea Forensics).

Dr. Kincaid has long been interested in hypotheses about the evolutionary and anthropogenic processes associated with the emergence and persistence of human pathogens and their concomitant diseases. Her doctoral work at Arizona State combined paleopathology, bioarchaeology, and genetics and employed enrichment strategies and short read sequencers to recover and reconstruct the genomes of ancient pathogens infecting once-living humans. She worked primarily on tuberculosis and leishmaniasis in the Americas, with experience in the genomes of plague and syphilis, as well as with non-infectious skeletal pathology. During her postdoctoral fellowship at UC Santa Cruz, she moved into NGS technology development.

QB3 Webinar: Christopher Ategeka. "The Unintended Consequences of Technology"

Scientists and entrepreneurs work every day to develop new technologies to meet society's needs. But every disruptive new technology is a double-edged sword that can have unintended consequences. Atomic energy brought the threat of annihilation. The internal combustion engine led to climate change. Social media has led to isolation. Now think about the promise of gene editing and other new life science technologies and where they might lead. How can we do our best to ensure that new technologies have the most favorable outcomes now and in the future? Join us to hear from author, entrepreneur, investor and TED speaker Christopher Ategeka.

WHERE & WHEN

Zoom Webinar
Wednesday, November 17, 2021, 1:00 to 2:00 PM PT

ABOUT THE SPEAKER

Christopher Ategeka is an award-winning engineer, entrepreneur, and an author.

He is the author of the book, titled "The Unintended Consequences of Technology" which focuses on the challenges and opportunities at the intersection of technology, humanity, and our planet.

He is also the founder and general partner at Startup playbook. A pre-seed fund that supports software startup companies run by women and other entrepreneurs traditionally underrepresented in the Venture Capital Market.

Before that, he was the founder and board chair at Health Access Corps, which focuses on strengthening healthcare systems in Africa using local talent to combat the extreme shortage of healthcare services in underserved regions. He has done this by building bicycle and motorcycle ambulances to facilitate the emergency transport of patients to health care facilities. He also built mobile clinics by refurbishing abandoned school buses converting them into "hospitals on wheels" to allow patients access to healthcare services in underserved areas of Africa.

He has won many international honors for his work: He was named to Forbes magazine’s “30 Under 30” list, Ashoka Fellow, TED Fellow, World Economic Forum Young Global Leader and most recently was honored by Chancellor Carol Christ and the UC Berkeley Foundation Board of Trustees with a 2021 Mark Bingham Award for excellence in achievement by a young alumnus in the last 10 years.

QB3 Webinar: Vasant Jadhav, Alnylam Pharmaceuticals. "Delivering on the Promise of RNAi Therapeutics"

Alnylam, based in Cambridge, MA, has led the translation of RNAi from Nobel Prize-winning discovery into an entirely new class of medicines. In 2018, their first medicine, ONPATTRO (patisiran), became the world’s first approved RNAi therapeutic. Their second medicine, GIVLAARI (givosiran), was approved in 2019, followed closely by OXLUMO (lumasiran), cleared in 2020. They are advancing a robust pipeline of innovative RNAi-based medicines in four therapeutic areas: genetic medicines, cardio-metabolic diseases, infectious diseases, and CNS and ocular diseases. Join us to learn how Alnylam conceives and develops therapies in this exciting new area.

Where & When

Zoom Webinar
1:00 to 2:00 PM PT, Wednesday, November 3, 2021

About the Speaker

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Dr. Vasant Jadhav is Senior VP, Research at Alnylam Pharmaceuticals. He has over 20 years of experience in the chemical biology research of nucleic acids spanning academic, biotech and big pharma industry for basic, diagnostic and therapeutic applications. He has a proven record of delivering insightful breakthroughs as an individual contributor and then growing in the role of team leader overseeing several large multi-disciplinary teams in highly collaborative and timely manner to deliver on the objectives.

Dr. Jadhav optimized fully modified siRNA technology and conceived novel siRNA designs, both key assets of Sirna Therapeutics. In addition, he managed collaborations with GSK and Allergan as a scientific lead in the field of respiratory and ocular diseases respectively.

He initiated, established and oversaw biology efforts of Merck’s industry leading siRNA conjugate delivery platform.  He led comprehensive efforts to engage internal and external scientific experts to unearth novel ways of enhancing cytosolic release of siRNA- the biggest barrier to fully realize potential of siRNA.

Dr. Jadhav earned his PhD from the National Chemical Laboratory in Pune, India, and completed a postdoctoral fellowship at the University of Colorado, Boulder.

QB3 Webinar: Gene Yeo, UCSD. "RNA-Binding Proteins as Regulators of Gene Expression, as Drugs, and as Drug Targets"

Gene Yeo’s lab at UC San Diego develops technologies and algorithms to explore how RNA-binding proteins (RBPs) influence RNA processing and how dysfunction is associated with human disease. Recently, Gene’s lab has been focused on developing RBPs as drugs and also as drug targets. Gene is a co-founder and member of the board of directors and scientific advisory board of Eclipse Bioinnovations, Enzerna, Locanabio, Trotana and Proteona. View Gene’s slide deck

Where & When

Zoom Webinar
1:00 to 2:00 PM PT, Wednesday, October 13, 2021

About the Speaker

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Gene Yeo PhD MBA is a Professor of Cellular and Molecular Medicine at the University of California San Diego (UCSD), a founding member of the Institute for Genomic Medicine and member of the UCSD Stem Cell Program and Moores Cancer Center. Dr. Yeo has a BSc in Chemical Engineering and a BA in Economics from the University of Illinois, Urbana-Champaign, a Ph.D. in Computational Neuroscience from Massachusetts Institute of Technology and an MBA from the UCSD Rady School of Management.

Dr. Yeo is a computational and experimental scientist who has contributed to RNA biology and therapeutics. His primary research interest is in understanding the importance of RNA processing and the roles that RNA binding proteins (RBPs) play in development and disease. Since inception, Dr. Yeo’s lab has focused on uncovering molecular principles by which RBPs affect gene expression, how RBP- mediated post-transcriptional gene networks contribute to cellular homeostasis in stem cells and the brain, and how mutations in RBPs lead to human developmental and neurodegenerative disease. His lab pioneered computational algorithms and experimental methods in human disease-relevant systems to conduct systematic and large-scale studies. These multidisciplinary methods combine machine learning, biochemistry, molecular biology, genomics, chemistry and materials research. His lab develops methods that are systematic, robust and adoptable, such as enhanced CLIP for the purposes of large-scale mapping of protein-RNA interactions (Van Nostrand et al, Nature Methods, 2016). Gene’s lab is a major contributor of resources to study RBPs that enable hundreds of labs across many areas of bioscience, such as the world’s largest resource of RBP-specific antibodies that facilitated generation and interpretation of the most comprehensive maps of RBP-binding sites to date for hundreds of RBPs (Van Nostrand et al, Nature, 2020). They have also systematically uncovered RBPs that condense into RNA granules during stress and demonstrated strategies to leverage these for therapeutic use in neurodegeneration (Markmiller et al, Cell, 2018; Fang et al, Neuron, 2019; Wheeler et al, Nature Methods, 2020). His lab also demonstrated in vivo RNA targeting with CRISPR/Cas proteins (Nelles et al, Cell, 2016) with proof of concept in repeat expansion disorders (Batra et al, Cell, 2017; Batra et al, Nature Biomedical Engineering, 2020). Work from the Yeo lab has been highlighted in Nature Methods and Nature Reviews Genetics as “Method to Watch” and featured as a top story in Discover magazine in 2016. These efforts have led to clinical programs to develop medicines for RNA-related diseases.

Dr. Yeo has authored more than 200 peer-reviewed publications including invited book chapters and review articles in the areas of neurodegeneration, RNA processing, computational biology and stem cell models; and served as Editor on two books on the biology of RNA binding proteins. Gene is on the Editorial Boards of the journals Cell Reports, Cell Research and eLife, and on the Advisory Board of Review commons. Gene joined UCSD as an Assistant Professor in 2008, was promoted with tenure to Associate Professor in 2014 and to Professor in 2016. Gene was the first Crick-Jacobs Fellow at the Salk Institute (2005-2008) and is a recipient of the Alfred P Sloan Fellowship in recognition of his work in computational molecular biology (2011), Alpha Chi Sigma-Zeta Chapter Krug Lecturer (2016), Singapore National Research Foundation Visiting Investigatorship Award (2017), the inaugural Early Career Award from the International RNA Society (2017), the Blavatnik National Award Finalist (2018 & 2019), San Diego Xconomy Awardee for ‘Big Idea’ (2019) and 2019 recipient of the Highly Cited Researcher in Cross-Field category, recognizing the world’s most influential researchers of the past decade. Gene’s research has been funded by the National Institute of Health, National Science Foundation, California Institute for Regenerative Medicine, TargetALS, ALS Foundation, Department of Defense, Myotonic Dystrophy Association, Myotonic Dystrophy Foundation and Chan-Zuckerberg Initiative. Gene has also been funded and collaborates with biotech and pharmaceutical companies such as Takeda, Genentech and Roche.

Gene is a co-founder of biotech companies which includes Locana, Eclipse Bioinnovations, Enzerna and Proteona. Gene played a critical role in the successful raising of $55M for Locana at series A (2019). Gene serves or had served on the scientific advisory boards of the Allen Institute of Immunology, Locana, Eclipse Bioinnovations, Proteona, Aquinnah, Cell Applications, Nugen (now Tecan), Sardona Therapeutics and Ribometrix. Gene is a senior advisor to Accelerator Life Sciences Partners.

Gene is the founder of the SCREEN (San Diego Covid-19 Research Enterprise Network, 2020) and founding member of the SEARCH (San Diego Epidemiology and Research for Covid Health, 2020) alliances in San Diego. SCREEN has ~1000 scientist members in San Diego focusing on grassroots research coordination and community outreach. SEARCH is focused on epidemiology studies of the prevalence of the virus completing a 12000-person study of viral spread. Gene is on the Return to Work task force in Biocom. Gene is the faculty founder of DASL (Diversity and Science Lecture Series, 2020) providing a voice for scientists to discuss diversity, equity and inclusion challenges and celebrating their scientific achievements. Gene was a Sword of Honor recipient (the highest honor) in Officer Cadet School in 1999 and has served in the Singapore Navy as a Naval officer. Gene has completed 2 full Ironman-distance and multiple half-ironman-, olympic-, sprint-distance triathlons, full marathons and half-marathons, but now spends time rock climbing.