Bio-IT World 2020 features five Informatics/Bioinformatics tracks focusing on Bioinformatics, Pharmaceutical R&D Informatics, Genome Informatics, Clinical Research & Translational Informatics, and Cancer Informatics. Click on each track to view its full agenda. Can't decide on a single track? Bio-IT World encourages track hopping to help attendees maximize their onsite experience.

CONFERENCE PROGRAMS


The Bioinformatics track assembles thought leaders who will present case studies using computational resources and tools that discuss the problems and challenges of taking data from multiple -omics sources and aligning it with clinical action. Turning big data into smart data can lead to real-time assistance in disease prevention, prognosis, diagnostics, and therapeutics. With the ever-increasing volume of information generated for curing or treating diseases and cancers, bioinformatics technologies, tools, and techniques play a critical role in turning data into actionable knowledge to meet unstated and unmet medical needs. Case studies will be presented on addressing these problems and challenges, including making the jump from prototyping to production code, defining what a "validated" informatics pipeline means, how to balance agility needs with requirements to be consistent/compliant, pipeline and workflow frameworks, containerization for reproducibility, and more. How do your approaches deal with inconsistencies in definitions and meta-data across the multiple datasets that form the basis of big data?

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Pharmaceutical R&D departments are at a crossroads – we have more technology and data than ever before, priming us for novel discoveries, yet there are still many challenges informatics strategies must address. The digitalization of the lab is at the forefront, and it necessitates quality data as well as knowledge management strategies, especially in the search for effective, real-world uses of AI and machine learning. We must also address how these new technologies are transforming day-to-day workflow and knowledge exchange, and what change management, investment, and regulatory strategies must be employed to make them successful. The Pharmaceutical R&D Informatics track will explore real-world projects related to digitalization, FAIR data, knowledge management systems, and artificial intelligence development and implementation, and how such initiatives are driving precision medicine.

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Biological information from genome sequences is derived by the application of computer and statistical techniques. Additionally, protein sequence and structure can be predicted by analyzing DNA sequence information. Tremendous advancements have been made to broaden sequencing applications from research to the clinic, especially as genomics becomes more integrated with precision medicine and AI initiatives. In spite of this, enormous problems still exist with data integration and analysis pipelines and sensitivity to accuracy in diagnosis and/or disease stratification. What is the role of computer science in modeling cells, analyzing and mapping data networks, and incorporating clinical and pathological data to determine how diseases arise from mutations? How do Bio-IT approaches help relate SNPs, expression, and disease? What is the role of AI in data curation techniques, text mining approaches, and statistical analytics to discover disease or drug response pathways to identify personalized and focused treatments and cures? Presentations in the Genome Informatics track will explore these issues and how organizations and research teams are implementing computational approaches to understand the biology of genomes.

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Advancing clinical trials and translational research requires transforming biological insights and raw research data into clean, actionable data for integration, visualization, and analysis. The Clinical Research and Translational Informatics track explores new and innovative tools and techniques—including big data analytics, machine learning, and artificial intelligence—and how they can be leveraged to address specific challenges faced across the drug discovery spectrum to accelerate the translation of scientific discoveries from the bench to medical care. Gain practical recommendations and real-world insights from case studies across pharma and academia. Actionable insights require making the results of complex analysis readily convertible into the common workflows of the clinician and researcher. How do you approach this problem?

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The Cancer Informatics track explores the important technology, informatics trends, and challenges of applying computational biology to cancer research and care. Themes that will be covered in expert-led presentations include: collaboration and network models; data access/management/integration strategies; and applications of biological interpretation to aid in research at the benchside or care at the bedside. Most clinical diagnoses involve the use of clinical testing, much of which is not standardized locally/nationally/internationally. How do your approaches address this reality?

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RECOMMENDED WORKSHOPS*

Workshop 1 - Data Management for Biologics: Registration and Beyond
The research IT systems that are used to support biologics pharma and biotech organizations are maturing to go beyond registration and support assay data collection, analytics and decision support. Additionally, new software providers are bringing forward innovative solutions to address structured data capture and automation. In this workshop we bring together some of the pharma, biotechs, and software providers who will share their approaches to registration and management of biologics data
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Workshop 3 - Introduction to Data Visualization for Biomedical Applications
In biology and other data-driven research areas, data visualization has become an integral part of the analysis toolkit. Data visualization approaches serve as the primary interface between analysts and the data. While great data visualization approaches can accelerate new discoveries, poor data visualization approaches can mislead and slow down progress. Participants of this introductory course will acquire the skills necessary to identify appropriate visualization methods for a given problem and learn about the state of the art in biological data visualization. This is an introductory course to the principles of data visualization.
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Workshop 9 - Digital Biomarkers and Wearables in Pharma R&D and Clinical Trials
There is a wealth of data in the form of digital information from sensors we use daily, from smart watches to fitness trackers, and this data has the potential to uncover new insight in the form of digital biomarkers. This workshop will cover the role of digital biomarkers in clinical trials and drug development, as well as technical challenges related to extracting data from sensors such as wearables and developing analytics, from the infrastructure to the algorithms. This workshop will also address the role of digital biomarkers in real-world practice in wellness programs and the pharmacy, and ultimately outline how digital biomarkers can advance personalized medicine.
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Workshop 12 - Cancer Genome Analysis
Cancer treatment is currently guided by the use of DNA- and RNA-sequencing. This use of sequencing is transforming the course of cancer therapy and greatly improving patient outcomes. This analysis is aided by large databases that have collected the sequencing data from tens of thousands of tumors. In this workshop, Dr. Rosenfeld will explain use of these databases both for research and clinical practice. After a simple tutorial, he will guide attendees through their own analysis of public tumor data and they will be able to perform their own studies without assistance. In addition, he will explain the procedures that are undertaken for the sequencing and interpretation of a tumor genome in a clinical context.
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Workshop 13 - Structuring Data for Drug Development and Regulatory Submissions: The Role of Standards and Ontology
Although the amount of chemical, biological, genetic and clinical data is rapidly increasing and the techniques for analyzing data are advancing, the lack of data standards and consistent data structures and ontologies often limits the utility and use of this data in drug development, regulatory and clinical decisions. This workshop will focus on four areas:

  • The development of global ISO data standards and tools to describe medicinal products,
  • The standardization and development of data structures and ontologies for bioassay data
  • NCATS is establishing the Biomedical Data Translator
  • The standardization of clinical laboratory data will focus on the SHIELD effort

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