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X-WR-CALDESC:We are pleased to announce the 13th in our series of meetings 
 on rare diseases\, which will present an exciting blend of genomic science
  and clinical medicine. This meeting will explore how cutting-edge genomic
  research translates into clinical care and informs our understanding of t
 he biology of rare disease.\n\nThe programme features the latest findings 
 related to the genomic basis of rare diseases\, providing powerful insight
 s into human biology\, disease mechanisms and therapeutic approaches. As g
 enomic sequencing becomes more available in the hospital setting\, we also
  examine the opportunities and challenges for clinical practice.\n\nThis y
 ear’s meeting will focus on large-scale whole genome sequencing studies an
 d discuss the intersection of polygenic and monogenic disorders and the im
 pact on our understanding of rare diseases. There will also be the opportu
 nity for bioinformaticians working in this area to showcase the innovative
  tools that they have developed. We will also include sessions on the lega
 l and ethical issues around sharing patient data and explore the new thera
 peutic approaches to rare diseases.\n\nThis conference provides an excelle
 nt multi-disciplinary forum for clinicians (consultants and trainees)\, re
 search and clinical scientists\, bioinformaticians and technology develope
 rs interested in understanding the impact of recent advances in genomics a
 nd technology on the care of patients with rare diseases.
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X-WR-TIMEZONE:America/New_York
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TZID:America/New_York
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TZNAME:EST
DTSTART:20191103T020000
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
RDATE:20201101T020000
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TZNAME:EDT
DTSTART:20200308T020000
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
RDATE:20210314T020000
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BEGIN:VEVENT
UID:483fba05-d075-4194-afe4-393b5afdafe5
DTSTAMP:20260428T231234Z
DESCRIPTION:We are pleased to announce the 13th in our series of meetings o
 n rare diseases\, which will present an exciting blend of genomic science 
 and clinical medicine. This meeting will explore how cutting-edge genomic 
 research translates into clinical care and informs our understanding of th
 e biology of rare disease.\n\nThe programme features the latest findings r
 elated to the genomic basis of rare diseases\, providing powerful insights
  into human biology\, disease mechanisms and therapeutic approaches. As ge
 nomic sequencing becomes more available in the hospital setting\, we also 
 examine the opportunities and challenges for clinical practice.\n\nThis ye
 ar’s meeting will focus on large-scale whole genome sequencing studies and
  discuss the intersection of polygenic and monogenic disorders and the imp
 act on our understanding of rare diseases. There will also be the opportun
 ity for bioinformaticians working in this area to showcase the innovative 
 tools that they have developed. We will also include sessions on the legal
  and ethical issues around sharing patient data and explore the new therap
 eutic approaches to rare diseases.\n\nThis conference provides an excellen
 t multi-disciplinary forum for clinicians (consultants and trainees)\, res
 earch and clinical scientists\, bioinformaticians and technology developer
 s interested in understanding the impact of recent advances in genomics an
 d technology on the care of patients with rare diseases.
DTSTART;TZID=America/New_York:20200325T000000
DTEND;TZID=America/New_York:20200328T235900
LOCATION:Wellcome Genome Campus\, UK
SUMMARY:Genomics of Rare Disease
END:VEVENT
END:VCALENDAR