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X-ORIGINAL-URL:https://www.med.unc.edu/flowcytometry
X-WR-CALDESC:Events for Flow Cytometry Core Facility
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DTSTART:20180311T070000
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BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190730T090000
DTEND;TZID=America/New_York:20190731T170000
DTSTAMP:20260404T031137
CREATED:20190529T172430Z
LAST-MODIFIED:20190712T175041Z
UID:10000139-1564477200-1564592400@www.med.unc.edu
SUMMARY:Flow Cytometry Boot Camp
DESCRIPTION:Two Day intensive advanced Flow Cytometry Training by Expert Cytometry\nTuesday-Wednesday July 30-31\, 2019 \nRegister here:  https://unc2019.eventbrite.com \n$500 for two days. \nUNC Flow Core users\, please email the core for a discount code to save $200. \nRegistration extended to 7/20/19. \nThis training is aimed at investigators who wish to improve their understanding of Flow Cytometry. The Introductory Flow Cytometry Training is a pre-requisite for UNC investigators. \n\nSyllabus:\nDay 1 \nPrinciples and best practices for compensation -Starting with the three rules of compensation\, this lecture will delve into the process of compensation\, and provide an understanding of the underlying assumptions of the three rules. \nEssential controls in cytometry – With the reproducibility crisis in science at the fore of peoples minds\, it is critical that your flow cytometry experiments contain the necessary controls for proper data interpretation.  Lacking these controls\, or overinterpreting a control can prove disastrous to your data. \nPractical 1:  Compensation practice – using a 5-color dataset with both beads and cells to practice automated compensation and while testing the assumptions of the three rules of compensation. \nData analysis – Data analysis starts during the experimental design process\, and ends with statistical analysis.  Learn what Capablanca meant by “In order to improve your game\, you must study the endgame before everything else.” \nDesigning experimental workflows – A flow cytometry experiment is more than adding some cells and antibodies together\, especially if the experiment will be part of a larger study.  This process includes the design\, optimization\, validation\, execution\, analysis and reporting of the final results. This lecture will focus on these steps and how each builds on the previous. \nPractical 2:  Data analysis – Using a high-dimensional dataset\, learn how to establish an analysis workflow\, along with some tips and tricks to make secondary analysis easier.\nTroubleshooting – Murphy’s law is bound to strike when you least expect it.  This lecture will cover some important concepts in identifying and solving some of the most common flow cytometry errors. \nDay 2 \nPanel Optimization – This lecture will focus on a deep dive on steps to help improve the quality of your flow cytometry panel.  This will cover topics including choosing the right machine\, implementing experimental controls and the theory of validation. \nPrinciples of Panel Design – The panel is central to the flow cytometry experiment.  Building on the concepts already presented\, this lecture will provide a theoretical guide to designing a flow cytometry panel using the information about the instrument\, fluorochromes and the cells. \nPractical 3:  Panel Design Exercise – Using the theory described in the course\, we will design a polychromatic panel designed to answer a pressing biological question.  With the information provided groups will design and present their best panels. \nAddressing reproducibility – Glen Begley described the fact that only 11% of 53 landmark oncology studies were reproducible.  With the time\, money and effort poured forth in biomedical research\, it is critical that we do better.  This lecture will use “Begley’s rules” to review the mindset for improving reproducibility. \nStatistical Analysis – When all is said and done\, flow cytometry data can be used to support or refute an experimental hypothesis.  This lecture will discuss some theory and considerations that should be considered for proper statistical analysis. \nRare event detection – With the ability to measure millions of events in short order\, flow cytometry is an ideal tool for looking for the cellular needle in the body’s haystack.  This lecture will cover three areas that are critical to monitor to be successful in rare event analysis. \nPrinciples of cell sorting – Isolation of cells for downstream applications\, especially genomic analysis\, is an extremely valuable tool for researchers.  Even if you are not running a cell sorter\, this lecture will provide practical tips for designing your next sorting experiment. \n  \n 
URL:https://www.med.unc.edu/flowcytometry/event/flow-cytometry-boot-camp/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190827T120000
DTEND;TZID=America/New_York:20190827T140000
DTSTAMP:20260404T031137
CREATED:20190715T224439Z
LAST-MODIFIED:20190716T222139Z
UID:10000140-1566907200-1566914400@www.med.unc.edu
SUMMARY:High Parameter Flow Cytometry Group
DESCRIPTION:Are you running flow cytometry experiments with more than 7 fluorophores? Do you want to go higher but are unsure of compensation and spreading error (what exactly is spreading again?)?  Are you ready to ditch boolean gating for tSNE but don’t know how to get started?  Join our High Parameter Flow Cytometry group. Bring your lunch and your laptop. This will be an ongoing group to help you with your flow cytometry panel design and data analysis.
URL:https://www.med.unc.edu/flowcytometry/event/high-parameter-flow-cytometry-group/
LOCATION:Marsico 5004
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190911T123000
DTEND;TZID=America/New_York:20190911T140000
DTSTAMP:20260404T031137
CREATED:20190910T151855Z
LAST-MODIFIED:20190910T151928Z
UID:10000142-1568205000-1568210400@www.med.unc.edu
SUMMARY:HIgh Parameter Flow Group
DESCRIPTION:Today’s meeting will focus on tools for panel design \nBring your lunch\, your laptop and your panel to discuss
URL:https://www.med.unc.edu/flowcytometry/event/high-parameter-flow-group/
LOCATION:5002 Marsico
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20190913T100000
DTEND;TZID=America/New_York:20190913T140000
DTSTAMP:20260404T031137
CREATED:20190903T150711Z
LAST-MODIFIED:20190903T150711Z
UID:10000141-1568368800-1568383200@www.med.unc.edu
SUMMARY:FCS Express training
DESCRIPTION:We will be having our Fall FCS Express Training on September 13\, 2019 in the Mary Ellen Jones Building Room 3112 from 10am-2pm (lunch will be provided for those who register).  Sarah Schuett with Denovo Software will be here to discuss getting started with the software\, working with plots\, gates\, stats\, spreadsheets and graphing\, batch processing\, compensation\, and transformations.  In the afternoon there will be time available for Q/A for our advanced users and/or you can book time with Sarah to discuss your specific layouts. \nThe link to register is:  https://denovosoftware.agilecrm.com/forms/5775503328673792
URL:https://www.med.unc.edu/flowcytometry/event/fcs-express-training/
LOCATION:3112 Mary Ellen Jiones Bldg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20191009T123000
DTEND;TZID=America/New_York:20191009T140000
DTSTAMP:20260404T031137
CREATED:20190910T152758Z
LAST-MODIFIED:20190910T152811Z
UID:10000143-1570624200-1570629600@www.med.unc.edu
SUMMARY:HIgh Parameter Flow Group
DESCRIPTION:Christian Aguilera-Sandoval from FlowJo will continue his tutorial on high parameter flow data analysis using custering algorithms. \nBring your lunch\, your laptop and your panel with data if you want to follow along.
URL:https://www.med.unc.edu/flowcytometry/event/high-parameter-flow-group-2/
LOCATION:3112 MEJB
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20191024T130000
DTEND;TZID=America/New_York:20191024T140000
DTSTAMP:20260404T031137
CREATED:20191018T174928Z
LAST-MODIFIED:20191018T175207Z
UID:10000148-1571922000-1571925600@www.med.unc.edu
SUMMARY:Fluorescence Compensation webinar
DESCRIPTION:“Advanced 4-18 Color Compensation Strategies For 2019” – Free webinar from Excyte \nThe webinar starts Thursday\, October 24th at 1 PM EDT. \nOne of the most common mistakes that has been passed down incorrectly by word of mouth over the years is the idea that it’s “okay” to do manual compensation. \nManual compensation is not okay. \nManual compensation is the process of adjusting the compensation based on how the data visually looks. \nIf you have manually compensated data in your lab notebook – strike it out\, and then redo your experiment. \nWhy? \nBecause manual compensation results in overcompensated data\, yielding incorrect conclusions. \nThe best practice is to use automatic compensation algorithms that are available in the most current versions of flow cytometry software. \nFor automatic compensation to be successful\, the following 3 rules must be followed: \n\nControls must be at least as bright as the samples they will be applied to. Brighter is better\, but not off scale.\n\n\nBackground fluorescence should be the same between the negative and positive population. Avoid using the universal negative for compensation.\n\n\nThe compensation color must be the same as the experimental color. For example\, don’t use Alexa488 to compensate for FITC.\n\nFollowing these three rules is easy when you’re doing a 1-color\, 2-color\, or even a 3-color flow cytometry experiment. \nHowever\, the process of compensating your experiment properly becomes much more complicated when you’re preparing 4-18 color experiments. \nFor this reason\, we’ve put together a rare\, FREE public webinar that will show you how to compensate 4-18 color experiments \n 
URL:https://www.med.unc.edu/flowcytometry/event/compensation-webinar/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20191105T130000
DTEND;TZID=America/New_York:20191105T140000
DTSTAMP:20260404T031137
CREATED:20191010T205928Z
LAST-MODIFIED:20191010T205928Z
UID:10000146-1572958800-1572962400@www.med.unc.edu
SUMMARY:Antibody validation for reproducible flow cytometry analysis
DESCRIPTION:Antibody validation for reproducible flow cytometry analysis \n30 minute webinar sponsored by Miltenyi Biotec \nProducing consistent data in flow cytometry experiments is a challenging endeavor. Besides instrument-related issues\, inconsistent reagents are a key source of irreproducible results. \nIn this webinar\, Mona Al-Maarri highlights how Miltenyi Biotec’s antibody production and validation efforts improve the quality and reproducibility of your flow cytometry results. In this 30-minute presentation\, you will learn about: \n\nThe antibody-related reproducibility crisis\nCommon causes of low reproducibility in flow cytometry experiments and lot-to-lot variations of antibody reagents\nRecombinant antibodies and how they improve reproducibility\nQuality control and validation steps employed in Miltenyi Biotec´s antibody production\n\nThere will be time for questions and discussion after the 30-minute webinar. \nNovember 5\, 2019\nEastern Standard Time 01:00 PM \nRegistration here \n 
URL:https://www.med.unc.edu/flowcytometry/event/antibody-validation-for-reproducible-flow-cytometry-analysis/
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20191106
DTEND;VALUE=DATE:20191109
DTSTAMP:20260404T031137
CREATED:20190917T203915Z
LAST-MODIFIED:20190917T203915Z
UID:10000145-1572998400-1573257599@www.med.unc.edu
SUMMARY:NERLSCD/MADSSCi 2019
DESCRIPTION:Exploring New Technologies to Drive Advances in Basic\, Clinical and Translational Research \nNovember 6-8\, 2019 Philadelphia PA
URL:https://www.med.unc.edu/flowcytometry/event/nerlscd-madssci-2019/
LOCATION:Philadelphia\, PA
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20191119T120000
DTEND;TZID=America/New_York:20191119T130000
DTSTAMP:20260404T031137
CREATED:20191108T021046Z
LAST-MODIFIED:20191108T021123Z
UID:10000150-1574164800-1574168400@www.med.unc.edu
SUMMARY:Flow Cytometry Best Practices - Lunch and Learn
DESCRIPTION:Ramiro Diz\, Ph.D.\, will present tips on best practices for flow cytometry experimental design\, data collection\, analysis and reporting. \nLunch will be provided by the Flow Core
URL:https://www.med.unc.edu/flowcytometry/event/flow-cytometry-best-practices-lunch-and-learn/
LOCATION:Pagano Conference Room\, 450 West Drive\, Chapel Hill\, NC\, United States
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20191205T110000
DTEND;TZID=America/New_York:20191205T120000
DTSTAMP:20260404T031137
CREATED:20191108T022732Z
LAST-MODIFIED:20191108T022901Z
UID:10000151-1575543600-1575547200@www.med.unc.edu
SUMMARY:FluoroFinder tutorial
DESCRIPTION:Live Tutorial/Webinar Dec 5th:\nIf you are new to FluoroFinder check out their Dec 5th webinar.  Anyone who registers will receive the recording as soon as the webinar ends\, even if they cannot attend the webinar. \nNew Spectra Viewer!\nFluoroFinder recently released a new Spectra Viewer! . \nwww.fluorofinder.com/ffsv/spectra_viewers
URL:https://www.med.unc.edu/flowcytometry/event/fluorofinder-tutorial/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200117T090000
DTEND;TZID=America/New_York:20200117T103000
DTSTAMP:20260404T031137
CREATED:20191114T194315Z
LAST-MODIFIED:20191219T221101Z
UID:10000152-1579251600-1579257000@www.med.unc.edu
SUMMARY:High dimensional cytometry with the Cytek Aurora
DESCRIPTION:Join us for a presentation on the new wave of Spectral Flow Cytometry. Learn what it is and how it is changing the landscape of flow cytometry world wide. \nThis is part of the Research Triangle Cytometry Association (RTCA) series. \nBagels and coffee provided by the Flow Core
URL:https://www.med.unc.edu/flowcytometry/event/high-dimensional-cytometry-with-the-cytek-aurora/
LOCATION:Pagano Conference Room\, 450 West Drive\, Chapel Hill\, NC\, United States
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200213T080000
DTEND;TZID=America/New_York:20200214T170000
DTSTAMP:20260404T031137
CREATED:20191018T145258Z
LAST-MODIFIED:20191018T145433Z
UID:10000147-1581580800-1581699600@www.med.unc.edu
SUMMARY:South East Flow Cytometry Interest Group (SEFCIG 2020)
DESCRIPTION:SEFCIG 2020\nOUR 11TH ANNUAL MEETING WILL BE FEBRUARY 13 &14 IN MOBILE\, ALABAMA  THIS IS DURING MARDI GRAS!!!  MOBILE IS THE BIRTHPLACE OF MARDI GRAS CELEBRATION IN THE US\, AND THIS IS A SPECIAL OPPORTUNITY TO ENJOY THE FESTIVITIES AND HEAR ABOUT THE LATEST ADVANCEMENTS IN THE WORLD OF CYTOMETRY.\nCONFIRMED SPEAKERS:\nJONNI MOORE\, UNIVERSITY OF PENNSYLVANIA\, PRESIDENT-ELECT ISAC\nPRATIP CHATTOPADHYAY\, NYU\nBILL TELFORD\, NCI\nJESSICA HOUSTON\, NEW MEXICO STATE UNIVERSITY\nTONY MARION\, UNIVERSITY OF TENNESSEE HSC\nDEREK JONES\, UNIVERSITY OF PENNSYLVANIA\nPETER LOPEZ\, NYU
URL:https://www.med.unc.edu/flowcytometry/event/south-east-flow-cytometry-interest-group-sefcig-2020/
LOCATION:Mobile\, AL
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20200229
DTEND;VALUE=DATE:20200304
DTSTAMP:20260404T031137
CREATED:20190917T203645Z
LAST-MODIFIED:20190917T203654Z
UID:10000144-1582934400-1583279999@www.med.unc.edu
SUMMARY:ABRF 2020 - Empowering Team Science
DESCRIPTION:The Association of Biomolecular Resource Facilities (ABRF) is pleased to invite you to join us for the 2020 ABRF Annual Meeting\, February 29 – March 3 in Palm Springs\, CA.  As the largest international organization representing shared resource cores\, the ABRF Annual Meeting is THE annual conference for technology-enabled multidisciplinary research. ABRF 2020 will offer an exciting mix of cutting edge science\, novel technology\, data science\, and the latest on rapidly evolving applications and methodology. \nThe 2020 ABRF Annual Meeting\, ABRF 2020: Empowering Team Science represents the collaborative energy of technology\, scientific research and core leadership. ABRF 2020 offers new programming options for and beyond the booth to drive traffic to the exhibitors\, and content integral to all core laboratories\, as well as targeted programming for Genomics\, Core Administration Leadership/Management\, Imaging\, Cytometry\, Bioinformatics\, and Mass Spectrometry enabled ‘Omics. Along with ample opportunities for networking\, collaboration and career development\, ABRF 2020 is the meeting to attend!
URL:https://www.med.unc.edu/flowcytometry/event/abrf-2020-empowering-team-science/
LOCATION:Palm Springs\, CA
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200402T090000
DTEND;TZID=America/New_York:20200402T100000
DTSTAMP:20260404T031137
CREATED:20200331T192215Z
LAST-MODIFIED:20200331T192310Z
UID:10000160-1585818000-1585821600@www.med.unc.edu
SUMMARY:Labroots Webinar: A Multi-Omic Approach to Detection and Characterization of Viral Pathogens and Their Impact on the Immune System
DESCRIPTION:Abstract \nA growing body of researchers around the world is working to mount an aggressive and sustained response to the COVID-19 pandemic. By building on past successes and harnessing insights from current efforts\, the scientific community will be better able to detect and characterize pathogens\, identify treatments\, and prepare for future outbreaks. \n  \nA comprehensive multi-omic approach is required to understand the complex biological mechanisms involved in SARS-CoV-2 infection\, improve the ability to detect and characterize the virus\, and assess the subsequent impact on the immune system and the response to therapeutic intervention. Fluidigm microfluidics-based genomic analysis tools and mass cytometry capabilities for highly multiplexed immune cell quantitation are uniquely enabling for virus detection and immune profiling of individuals and will be increasingly important to government and medical institutions. In this presentation\, we will describe our genomic analysis solutions for PCR- and NGS-based applications leveraging the benefits of nanoliter-scale automated microfluidics technology. We will also present the best-in-class immune profiling and monitoring capabilities of mass cytometry\, powered by our CyTOF® technology. Our discussion will reflect the use of these tools in research efforts currently underway. \n  \nRegister here
URL:https://www.med.unc.edu/flowcytometry/event/labroots-webinar-a-multi-omic-approach-to-detection-and-characterization-of-viral-pathogens-and-their-impact-on-the-immune-system/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200402T130000
DTEND;TZID=America/New_York:20200402T140000
DTSTAMP:20260404T031137
CREATED:20200401T134212Z
LAST-MODIFIED:20200401T134213Z
UID:10000162-1585832400-1585836000@www.med.unc.edu
SUMMARY:Intro to FlowJo
DESCRIPTION:“Hi everyone\, this is Christian Aguilera-Sandoval\, your FlowJo Application Scientist.  On Thursday April 2\, 2020 at 1pm EST\, I will be hosting a webinar on Intro to FlowJo. I would be great if you and your FlowJo users could join me and learn more or get a refresher on FlowJo v10. You do not need to have a license to view/join our webinars. All you need to do is register at” \nhttps://lnkd.in/e85VvpY
URL:https://www.med.unc.edu/flowcytometry/event/intro-to-flowjo/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200414T120000
DTEND;TZID=America/New_York:20200414T130000
DTSTAMP:20260404T031137
CREATED:20200409T142440Z
LAST-MODIFIED:20200409T142440Z
UID:10000165-1586865600-1586869200@www.med.unc.edu
SUMMARY:Introduction to the Cytobank platform and machine learning algorithms
DESCRIPTION:Join us for an introduction to data analyses and data management within the Cytobank platform \n  \nBootcamp Session 1
URL:https://www.med.unc.edu/flowcytometry/event/introduction-to-the-cytobank-platform-and-machine-learning-algorithms/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200416T120000
DTEND;TZID=America/New_York:20200416T130000
DTSTAMP:20260404T031137
CREATED:20200409T142603Z
LAST-MODIFIED:20200409T142603Z
UID:10000163-1587038400-1587042000@www.med.unc.edu
SUMMARY:Cytobank Platform in-app introduction
DESCRIPTION:Join this session to learn specifics on data security\, data pre-processing\, exporting statistics\, and figure generation within the Cytobank platform \n  \nBootcamp Session 2
URL:https://www.med.unc.edu/flowcytometry/event/cytobank-platform-in-app-introduction/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200420T093000
DTEND;TZID=America/New_York:20200420T150000
DTSTAMP:20260404T031137
CREATED:20200116T142841Z
LAST-MODIFIED:20200324T184758Z
UID:10000154-1587375000-1587394800@www.med.unc.edu
SUMMARY:POSTPONED due to Covid19  - FlowJo Cytometry Analysis Software Training
DESCRIPTION:This event has been postponed to a later date\, TBD.  – Please refer to FlowJo’s online content for help\, or contact the flow core for remote assistance. \n  \nChristian Aguilera-Sandoval will provide training for FlowJo software. \nMorning session – introductory and advance data analysis \nAfternoon – Spectral Flow Cytometry analysis\, High Parameter analysis with clustering algorithms (tSNE\, etc)
URL:https://www.med.unc.edu/flowcytometry/event/flowjo-cytometry-analysis-software-training/
LOCATION:G405 Koury
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200421T120000
DTEND;TZID=America/New_York:20200421T130000
DTSTAMP:20260404T031137
CREATED:20200409T142713Z
LAST-MODIFIED:20200409T142713Z
UID:10000161-1587470400-1587474000@www.med.unc.edu
SUMMARY:Dimension reduction with viSNE
DESCRIPTION:Come join us for a demonstration on how to set up viSNE\, optimize it and interpret the results within the Cytobank platform. \n  \nBootcamp Session 3
URL:https://www.med.unc.edu/flowcytometry/event/dimension-reduction-with-visne/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200423T120000
DTEND;TZID=America/New_York:20200423T130000
DTSTAMP:20260404T031137
CREATED:20200409T142836Z
LAST-MODIFIED:20200409T142836Z
UID:10000159-1587643200-1587646800@www.med.unc.edu
SUMMARY:Clustering with FlowSOM
DESCRIPTION:This session will take you through the FlowSOM algorithm; how to set it up\, when to use it and combining FlowSOM with viSNE. \n  \nBootcamp Session 4
URL:https://www.med.unc.edu/flowcytometry/event/clustering-with-flowsom/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200423T120000
DTEND;TZID=America/New_York:20200423T130000
DTSTAMP:20260404T031137
CREATED:20200407T160418Z
LAST-MODIFIED:20200409T143300Z
UID:10000164-1587643200-1587646800@www.med.unc.edu
SUMMARY:A Solid Foundation for Simpler and Smarter Panel Design
DESCRIPTION:BD Presents a Seminar on using a BD Harmony to enhance your flow experiments. See more details and register here https://event.on24.com/wcc/r/2261951/7AEF02176AB4EF2E778513D051413E97
URL:https://www.med.unc.edu/flowcytometry/event/a-solid-foundation-for-simpler-and-smarter-panel-design/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200428T120000
DTEND;TZID=America/New_York:20200428T130000
DTSTAMP:20260404T031137
CREATED:20200409T142936Z
LAST-MODIFIED:20200409T142936Z
UID:10000157-1588075200-1588078800@www.med.unc.edu
SUMMARY:Biomarker discovery with CITRUS
DESCRIPTION:Join us in learning how to utilize CITRUS algorithm for identification of differences between experimental groups. \n  \nBootcamp Session 5
URL:https://www.med.unc.edu/flowcytometry/event/biomarker-discovery-with-citrus/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200429T110000
DTEND;TZID=America/New_York:20200429T140000
DTSTAMP:20260404T031137
CREATED:20200129T214412Z
LAST-MODIFIED:20200324T184853Z
UID:10000156-1588158000-1588168800@www.med.unc.edu
SUMMARY:POSTPONED - Flow Cytometry Education and Outreach Day
DESCRIPTION:This event will be rescheduled for a later date. \n  \nJoin us to learn about Flow Cytometry offerings at UNC and meet with vendors of reagents to help you plan your experiments. \nLunch and door prizes!!
URL:https://www.med.unc.edu/flowcytometry/event/flow-cytometry-education-and-outreach-day-2/
LOCATION:MBRB Lobby and 2nd floor
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200429T130000
DTEND;TZID=America/New_York:20200429T140000
DTSTAMP:20260404T031137
CREATED:20200423T133049Z
LAST-MODIFIED:20200423T133049Z
UID:10000168-1588165200-1588168800@www.med.unc.edu
SUMMARY:How to Perform Spectral Unmixing with FCS Express 7
DESCRIPTION:
URL:https://www.med.unc.edu/flowcytometry/event/how-to-perform-spectral-unmixing-with-fcs-express-7/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200430T120000
DTEND;TZID=America/New_York:20200430T130000
DTSTAMP:20260404T031137
CREATED:20200409T143107Z
LAST-MODIFIED:20200409T143107Z
UID:10000166-1588248000-1588251600@www.med.unc.edu
SUMMARY:Apply machine learning algorithms to non-cytometry data
DESCRIPTION:Join this session to learn how to analyze other types of single-cell data\, including CITE-seq and Single-cell RNA-seq data. \n  \nBootcamp Session 6
URL:https://www.med.unc.edu/flowcytometry/event/apply-machine-learning-algorithms-to-non-cytometry-data/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200430T130000
DTEND;TZID=America/New_York:20200430T140000
DTSTAMP:20260404T031137
CREATED:20200417T180411Z
LAST-MODIFIED:20200417T180411Z
UID:10000167-1588251600-1588255200@www.med.unc.edu
SUMMARY:Applying Panel Design Principles to Investigate COVID-19 Immune Response with the Cytek Aurora
DESCRIPTION:Upcoming Webinar\n\n\n\n\n\n\n\n\n\n\n\n\n\nJoin us on Thursday\, April 30th\, 10AM PST for our next webinar: Applying Panel Design Principles to Investigate COVID-19 Immune Response with the Cytek Aurora. We’ll begin with an overview of the system and its features\, and then dive in to panel design principles and guidance on how to adapt our 35 color panel to your research applications
URL:https://www.med.unc.edu/flowcytometry/event/applying-panel-design-principles-to-investigate-covid-19-immune-response-with-the-cytek-aurora/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200511T120000
DTEND;TZID=America/New_York:20200511T130000
DTSTAMP:20260404T031137
CREATED:20200506T161706Z
LAST-MODIFIED:20200506T162102Z
UID:10000155-1589198400-1589202000@www.med.unc.edu
SUMMARY:ISAC Live Webinar Adaptive Immunity: Memory\, Protection\, and Immunopathology in COVID-19
DESCRIPTION:About the Presenter \nProfessor Andreas Radbruch is a biologist by training\, having done his Ph.D. at the Genetics Institute of Cologne University.  He has been the Director of the German Rheumatism Research Centre Berlin\, a  Leibniz institute\, since 1996 and Professor of Rheumatology at the Charité Medical School of the Humboldt University of Berlin since 1998.  Andreas Radbruch is a former President of ISAC and the current President of the European Federation of Immunological Societies (EFIS). \nWebinar Description \nThe situation that we are facing with the COVID-19 pandemic is unprecedented. The IUIS is collaborating with Frontiers and launching a series of weekly expert commentaries and scientific webinars to accelerate the development of novel diagnostics\, therapeutics and vaccines. \nWhat do we know about the adaptive immune reaction to Sars-CoV-2?  Why do humans react so heterogeneously to Sars-CoV-2?  Does the adaptive immune system provide protection and for how long?  How can we challenge the system with a vaccine to establish longlasting\, efficient immunity?
URL:https://www.med.unc.edu/flowcytometry/event/isac-live-webinar-adaptive-immunity-memory-protection-and-immunopathology-in-covid-19/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200519T110000
DTEND;TZID=America/New_York:20200519T120000
DTSTAMP:20260404T031137
CREATED:20200515T150829Z
LAST-MODIFIED:20200515T150829Z
UID:10000118-1589886000-1589889600@www.med.unc.edu
SUMMARY:Microfluidic Sorting of Biohazardous Material on the MACSQuant Tyto
DESCRIPTION:Join our webinar as we discuss: \n\n•Gentle sorting in a closed cartridge system without sheath fluid \n•Operator safety (no aerosols or droplet formation) \n•Intuitive handling suitable for any lab professional \n•Biohazardous sorting data sets (anaerobic bacteria\, T cell subsets from HIV infected PMBC\, Plasmodium bergei sporozoites\, Pichia pastoris yeast\, and E. Coli bacteria)
URL:https://www.med.unc.edu/flowcytometry/event/microfluidic-sorting-of-biohazardous-material-on-the-macsquant-tyto/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200522T130000
DTEND;TZID=America/New_York:20200522T140000
DTSTAMP:20260404T031137
CREATED:20200515T145213Z
LAST-MODIFIED:20200515T145438Z
UID:10000115-1590152400-1590156000@www.med.unc.edu
SUMMARY:Tips and Tricks in FCS Express 7
DESCRIPTION:Join us for a potpourri of handy tips and tricks to enhance your analysis experience in FCS Express 7. We’ll cover things like keyboard shortcuts for oft-executed actions\, easy ways for formatting multiple plots or your entire layout at once\, displaying and sorting on keyword metadata within the layout\, choosing and tweaking axis scaling\, commonly edited default User Options\, and more. Plus\, as usual\, there will be several minutes reserved for Q&A\, so we can address anything else of special interest to you!
URL:https://www.med.unc.edu/flowcytometry/event/tips-and-tricks-in-fcs-express-7/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200527T130000
DTEND;TZID=America/New_York:20200527T140000
DTSTAMP:20260404T031137
CREATED:20200515T145342Z
LAST-MODIFIED:20200515T145342Z
UID:10000116-1590584400-1590588000@www.med.unc.edu
SUMMARY:The Importance of Iteration Management for Batch Processing
DESCRIPTION:Iterations determine the logic by which the Batch Process advances through your data files. In this webinar\, we will learn how to effectively manage iterations in FCS Express. We will begin by defining what an iteration is\, how to determine if iterations are active (i.e.\, available for the Batch Process)\, and uncovering common practices that inactivate iterations. The Data Navigator will be introduced as a tool to restore active iterations. We will also explore how Panels can redefine the number of data files per iteration\, for more complex analysis strategies. We will then review Batch Processing Options\, inspect how to manipulate iterations for output files\, and run the Batch Process
URL:https://www.med.unc.edu/flowcytometry/event/the-importance-of-iteration-management-for-batch-processing/
END:VEVENT
END:VCALENDAR