BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//Ignite II - ECPv6.15.20//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:Ignite II
X-ORIGINAL-URL:https://gmkb.org
X-WR-CALDESC:Events for Ignite II
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:America/New_York
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:20210314T070000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:20211107T060000
END:STANDARD
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:20220313T070000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:20221106T060000
END:STANDARD
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:20230312T070000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:20231105T060000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20220822T120000
DTEND;TZID=America/New_York:20220822T130000
DTSTAMP:20260427T122031
CREATED:20220819T193703Z
LAST-MODIFIED:20220819T193703Z
UID:2661-1661169600-1661173200@gmkb.org
SUMMARY:PTEN hamartoma tumor syndrome: A personalized healthcare journey
DESCRIPTION:PTEN hamartoma tumor syndrome: A personalized healthcare journey \nMonday\, August 22 | 12-1 p.m. ET | Virtual \nCharis Eng\, MD\, PhD\, FACP\, is a leader in the field of cancer genetics. She was the first to discover a link between mutations in the cancer suppressor gene PTEN and Cowden syndrome and other disorders that can put patients at an increased risk for several types of cancer. Read more about her work in this Q&A with Dr. Eng. \nThis lecture is part of the Precision Genomic Collaboratory’s Genomic Seminar Series\, a quarterly seminar series that highlights leading researchers and their high-level vision for genetics\, genomics\, and ‘omics broadly. \nLearn more about Dr. Eng’s virtual lecture on the Genomic Seminar Series website.
URL:https://gmkb.org/event/pten-hamartoma-tumor-syndrome-a-personalized-healthcare-journey/
LOCATION:Virtual
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20220825T110000
DTEND;TZID=America/New_York:20220825T120000
DTSTAMP:20260427T122031
CREATED:20220809T193910Z
LAST-MODIFIED:20220921T142943Z
UID:2630-1661425200-1661428800@gmkb.org
SUMMARY:The Routine Failure to Clinically Identify Monogenic Cases of Common Disease in Clinical Practice
DESCRIPTION:CDC Webinar – The Routine Failure to Clinically Identify Monogenic Cases of Common Disease in Clinical Practice: Addressing Diagnostic Misattributions and Errors\nThursday\, August 25 | 11 a.m. – 12 p.m. ET  | Virtual \nChanges in clinical and laboratory practice are needed to improve the diagnosis of monogenic forms of common diseases. This webinar seeks to focus attention on the need for universal genetic testing in common diseases for which the recommended clinical management of patients with specific monogenic forms of disease diverges from standard management and has evidence for improved outcomes. \nPlease note: registration is required. Visit the CDC’s website to learn more and sign up.
URL:https://gmkb.org/event/the-routine-failure-to-clinically-identify-monogenic-cases-of-common-disease-in-clinical-practice/
LOCATION:Virtual
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20220831T110000
DTEND;TZID=America/New_York:20220901T170000
DTSTAMP:20260427T122031
CREATED:20220715T131309Z
LAST-MODIFIED:20220921T142703Z
UID:2556-1661943600-1662051600@gmkb.org
SUMMARY:Genomic Medicine XIV: Genomic Learning Healthcare Systems
DESCRIPTION:Genomic Medicine XIV: Genomic Learning Healthcare Systems\nWednesday\, August 31 – Thursday\, September 1\, 2022 | 11 a.m. – 5 p.m. ET | Virtual \nOn August 31 – September 1\, 2022\, the National Human Genome Research Institute (NHGRI) will sponsor its 14th Genomic Medicine meeting\, Genomic Medicine XIV: Genomic Learning Healthcare Systems. \nThis meeting will discuss progress and identify generalizable solutions to the challenges of implementing genomic medicine we have encountered since the 2015 National Academy of Medicine’s Genomics-Enabled Learning Health Care Systems workshop. Persistent barriers and evidence gaps will be examined as opportunities for additional research.
URL:https://gmkb.org/event/genomic-medicine-xiv-genomic-learning-healthcare-systems/
LOCATION:Virtual
END:VEVENT
END:VCALENDAR