World orphan drug congress 2020 2 5 november 2020 terrapinn. During the webinar, amy discusses the most common types of hereditary heart diseases, including coronary heart. Genetic alliance offers this series of monthly webinars, on the second tuesday of each month at noon, beginning in february 20 and ending in december. After viewing this 1hour webinar, learners will be able to. An overview of ftd genetics and the role of genetic counseling. All of our webinars are available on our youtube channel.
The alliance is a recognized leader for providing education to the organ donation and transplantation community. Betty jeans story forensic genealogy, dna and adoption. We support and develop communities by providing an excellent range of services to our members, new groups and everyone affected by these conditions. Jan 17, 2015 the 15 best webinar software products from around the web posted on january 17, 2015 by b. Genetic alliance has and will continue to host a number of featured webinar.
Benjamin solomon and assistant director of neurogenetics, dr. Softgenetics software powertools for genetic analysis. The ts alliance is dedicated to finding a cure for tuberous sclerosis complex, while improving the lives of those affected. Click on the link below to discover why you should host a webinar and how it can. The alliance has hosted more than 30 webinars on thematic areas of interest and relevance to social service provision and workforce strengthening across many stakeholder groups. We work with our members on campaigns, consultations and engagement projects to ensure our work accurately reflects the needs and concerns of patients and families affected by all types of genetic conditions. The 15 best webinar software products from around the web. Genetic alliance improves health systems through novel partnerships and the dynamic engagement of communities and individuals. Genetic analysis webinars thermo fisher scientific fr. Apr 17, 2018 genetic alliance has and will continue to host a number of featured webinar series in order to offer a forum for professionals and lay people to hear about new programs and policies in genetic medicine. Join the genetic alliance uk policy team, on december, 10. Click on a previous webinar to read a summary and listen to a recording.
The platform for engaging everyone responsibly peer is a community engagement and data collection. During the webinar, amy discusses the most common types of hereditary heart diseases, including coronary heart disease and heart attacks, aneurysms, abnormal heart rhythms called arrhythmias, a very common form of hereditary high cholesterol called familial hypercholesterolemia, as well. This virtual platform enables the active exchange of information and expertise across and within countries and provides a costeffective method of identifying and. Empowering individuals as advocates genetic alliance. Genetic alliance south africa gasa is a nonprofit, membership organisation uniting patient support groups, healthcare professionals and other stakeholders relevant to the care and prevention of congenital disorders. For one year from the date of software release, the contractor shall. Registries for all reg4all is an innovative new registry platform that aims to. In general, the webinars will last one hour and leave ample time for questions and answers. The genetic counselors and you series turns complex genetics into information you can use for your personal healthcare. Webinars the association for x and y chromosome variations. Please note that some features may not function properly. This webinar is presented by rebecca miller, genetic counselor at inova translational medicine institute,along with our managing director, dr. These genetic results, sharpened by oriens clinical data and the significant size of the sample set, accurately elucidate known drivers of cancer, identify new genetic alterations, and reveal novel potential therapeutic targets. The genetic counselors and you series is now available as a podcast subscribe by searching for genetic counselors.
The following webinar is presented by amy sturm, cgc lgc. The webinars listed below will introduce you to technologies and. This webinar is free and open to all genetic alliance uk members and rare disease uk supporters. We are an alliance of over 200 patient organisations providing information and support for patients affected by genetic and rare conditions. Clinical genetic and genomic testing for autism and related disorders. This webinar walks you through the all new online advocacy atlas highlighting resources around advocacy and leadership, employment success. The genetic alliance uk submitted a presentation entitled the wales webinar on the consultation on the uk plan for rare diseases the alliance believes that everyone living with a rare disease should be able to receive high quality services, treatment and support. Genetic solutions are being applied within the fields of human identity testing, oncology research, infectious disease research, pharmacogenomics, and inherited disease research to name a few.
The focus of the software is to infer tree models that relate genetic aberrations to tumor progression. Visit our webinar archive for previous webinar recordings and presentations. Mdas genetic counseling webinar, which occurred feb. We use cookies and tracking to improve your browsing experience on our website, to analyze our website traffic, and to understand where our visitors are coming from.
All webinars are free of charge and are also archived for later viewing. We invite your suggestions for future webinar topics and speakers. Her presentation focuses on the importance of the family history. Genetic alliance webinars offer information and discussion on a variety of topics, including hotbutton issues in genetics and advocacy, public policy, and. Respondents to mdas transitions survey in other words, people with a neuromuscular disease who are in their teens through late 30s made it clear they had questions about the genetics of their disease, as well as questions about family planning and the value of diagnostic testing. Ambry genetics has joined institutional partnersincluding the diagnostic. This webinar is a mustsee for anyone seeking to reduce the cost of sequencing from gene expression studies or who wish to perform pilot studies inexpensively. Program director, office of rare diseases research. This webinar is brought to you by the science aaas custom publishing office. Cris kinross of thermo fisher scientific provides an overview of the differences between 3 mrnaseq, mrnaseq, and wholetranscriptome sequencing. There iswas a problem with your internet connection.
This printable guide from the genetic alliance is a paper based tool that helps you gather. The webinars listed below will introduce you to technologies and applications that are advancing scientific research. The software is designed to analyze data generated by a technique called comparative genomic hybridization, but it has also been used to analyze cytogenetic breakpoint data. To help you, genetic alliance hosted a webinar with heather joseph of. An introduction to the analysis of deep sequencing data using clc bios genomics workbench and genomics server presented by rob mervis, field applications scientist at clc bio march 20th at 10am in holden auditorium this will be an interactive demonstration and discussion of the various applications and workflows that can be performed on deep sequencing. Information for patient organisations genetic alliance uk. This webinar focuses on a recent genetics in medicine publication that showed a strong association of breast cancer in patients with a pathogenic variant in lynch syndrome genes. Webinar series organ donation and transplantation alliance. If youre or a small business or startup looking to implement webinar solutions at minimum cost, heres a list of 6 highquality free webinar software used by a large number of people. You can try out each of the best free webinar software for startups and opt for the most userfriendly option that suits your business needs.
We supply 40% of the commercial hog market in ontario with genetics the largest market share of any company. Agc offers the best genetic package in the industry. From regulatory matters to donor management and transplant practices, you will find a webinar topic that meets your needs and improves your knowledge. Jul 31, 20 most of the rest of the webinar will use the term patient. Develop an accessible webopen source softwarebased patient registry. An overview of ftd genetics and the role of genetic. Webinar playlist on the official axys youtube channel conference and webinar presenters share their professional and personal opinions. Matloff describes which patients are candidates for genetic. An overview of ftd genetics and the role of genetic counseling march 22, 2018 emily dwosh from ubc hospital clinic for alzheimer disease and related disorders explores how genetic counseling can help support individuals and families as they adjust to an ftd diagnosis. As part of these settings, peer also features content from communitybased guides. Information blocking, and the onc health it certification program rule, june 3, 2019. This webinar will present screener for mechanistic analysis, a software solution that ensures consistent and reliable processing of mechanistic high throughput assays, with the potential to dramatically increase the yield of highquality lead candidates. Applying genetic biomarkers to personalize treatments.
Resource provider opportunities parent project muscular dystrophy. Learn about genetics there are over 6,000 genetic conditions caused, at least partly, by changes in the dna. Harb, md, facs, fascrs, is a boardcertified colorectal surgeon, specializing in the treatment of diseases of the colon and continue reading. Alliance for hope international hosts a variety of onsite trainings and events, webinar, and conference calls. Nextgene software is the perfect analytical partner for the analysis of desktop sequencing data produced by illumina iseq, miniseq, miseq, nextseq, hiseq, and novaseq systems, ion torrent ion genestudio s5, pgm, and proton systems as well as other platforms. A replay of each webinar will be available shortly after the live session so you can share with those unable to attend the live session. Genetic alliance webinars offer information and discussion on a variety of topics, including hotbutton issues in genetics and advocacy, public policy, and organizational development. Bring programming questions to the live sessions for our technical experts to answer. Genetic alliance has and will continue to host a number of featured webinar series in order to offer a forum for professionals and lay people to hear about new programs and policies in genetic medicine. Includes dfm, dfa, material and process selection advice and recommended analysis work to ensure robustness. Understanding rare disease registries global genes. The role of the social service workforce in supporting children on the move.
The platform was developed by genetic alliance in 2011 in partnership with private access, inc. Emily dwosh from ubc hospital clinic for alzheimer disease and related disorders explores how genetic counseling can help support individuals and families as they adjust to an ftd diagnosis. See the link below for an archive of informative webinars featuring presentations by professionals in various fields relating to x and y chromosome variations. Genetic alliance south africa gasa is a nonprofit, membership organisation uniting patient support groups, healthcare professionals and other stakeholders. Genetic analysis webinars thermo fisher scientific us. The alliance provides training on numerous topics including domestic violence, sexual assault, strangulation prevention, adverse childhood conditions aces, trauma informed care, leadership, sustainability and more. Program for engaging everyone responsibly genetic alliance. Farhana ali, our public affairs manager, lead the webinar, to inform patient organisations and rare disease uk supporters on our exciting new concept for rare disease day 2019 and how to get involved. In the course of running a blog or owning a business, there is probably going to come a time when putting on a webinar is necessary.
The alliance hosts several monthly webinar programs on the latest cuttingedge and timely topics impacting the donation and transplant community. Alliance genetics products and services consistently deliver the highest genetic gains in the swine business, thanks to our purebred nucleus the largest in canada. Clinician or health professionalreported data the addition of some clinicianentered data andor data from medical records and laboratory tests is optimal, but not always. Keeton in resources 91 comments in the course of running a blog or owning a business, there is probably going to come a time when putting on a webinar is necessary. Making your organizations registry andor biobank a reality. This year you will be able to access and personalise resources, for example, to raise awareness. The first webinar of 2020 will provide an overview of whos executive board 146th session including updates on cervical cancer elimination, alcohol control, eye care and involvement of nonstate actors in whos governing bodies, a recap of the global ncd alliance forum 2020 and information about how to engage on world obesity day 4 march. We are an alliance of over 200 patient organisations. Data sources for a patient registry patientreported data patients live with diseases every day and can provide very accurate information about their experiences, patientreported outcomes, quality of life, etc. Oct 16, 2012 the genetic alliance uk submitted a presentation entitled the wales webinar on the consultation on the uk plan for rare diseases the alliance believes that everyone living with a rare disease should be able to receive high quality services, treatment and support. Using the igs feeder profit calculator, cattlemen are able to provide sire information, regardless of breed, as well as preconditioning, weaning and health data in exchange for a total relative value that compares the profit potential of their calves to the industry at large.
More than 1 in every 100 people has a genetic predisposition to a hereditary type of heart disease. In this page, you can find information about dna, genes and genomes and genetic conditions. Forum established by the advocacy and community organizations around special topics offer workgroups to dive into. Some of the unique aspects of garb are its lack of commercial interests and continual improvements in response to the needs of its members. A replay of each webinar will be available shortly after the live session so you. Except where otherwise noted, content on this site is licensed under a creative commons attribution 3. From newborn screening to genetic testing regulation, family health history, and tools for running an advocacy organization. During this webinar youll learn more about the rapid progress being made in linking genetic testing and personalized medicine to better health outcomes. Useful links overview genetic alliance south africa gasa is a nonprofit, membership organisation uniting patient support groups, healthcare professionals and other stakeholders relevant to the care and prevention of congenital disorders. Family history tools heartland regional genetics network.
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