The Nordic Alliance for Sequencing and Personalized Medicine is an independent, non-governmental, not-for-profit, Nordic association that has received initial funding from Nordforsk. The overall mission is to share trustworthy genomics data and technology competence for improved diagnosis and treatment, and as a resource for research.
On behalf of the organising committee it is my pleasure to invite you to the first meeting of the Nordic Alliance for Sequencing and Personalised Medicine. We are excited to share the attached agenda which includes prominent speakers from the Nordics and beyond. The meeting is arranged in cooperation with Nordforsk and will take place 15.-16. November 2017 at the Veritas centre, Høvik, Norway. Please register for the meeting here within 1. November, no participation fee.
Organising committee:

  • Dag E. Undlien, Oslo University Hospital
  • Joakim Lundeberg, SciLifeLab
  • Valtteri Wirta, SciLifeLab
  • Stephen McAdam, DNV GL

Participation in the consecutive workshops on day two are for Nordic Alliance Members and invitations handled separately. 

Time and place: Nov. 2, 2017 9:30 AM - 4:00 PM, 5th floor, Ole Johan Dahls hus  

The workshop will feature presentations by leading international researchers in the field, as well as presentations on on-going work that addresses this problem. The workshop will furthermore provide a meeting-place for both academic and industrial partners with an interest in clinical NLP with the aim to stimulate further collaboration.

More information at the workshop web page: https://www.mn.uio.no/ifi/english/research/news-and-events/events/bigmed-workshop.html

 

Big Data
Big Data i helsetjenesten- rettslige aspekter

Vi ønsker med dette å invitere deg til å delta på konferansen, og til å bidra med et foredrag og/eller et vitenskapelig bidrag, på et skandinavisk språk.  

Konferansen har som mål å samle aktører som befatter seg med digitalisering av helsetjenesten, og akademiske miljøer i de nordiske land, for å dele erfaringer og ekspertise, samt å få diskutert og belyst utfordringer og muligheter innenfor dette nye rettsfeltet.  

Vi ønsker aktører i juridiske fagmiljø i offentlig og privat virksomhet/samfunnsliv til å presentere foredrag om aktuelle tema og til å levere notater med problemsstillinger (paper) og artikler. Det samme ønsker vi fra forskere, i tillegg til at det er en anledning til å legge frem pågående forskningsprosjekter og/eller resultater eller artikler.

Presentasjoner fra møtet:

IT-løsninger for mer presis pasientbehandling 
Arbeidspakke 5, Juss og etikk
Juridiske teamer

 

Job announcement from DNV GLArbeidsgiverDNV GLStillingstittelSenior Researcher - Life SciencesStedOslo, NorwayFrist16.07.2017VarighetFast

Bli kjent med DNV GL

The ideal candidate has both big picture understanding of personalized medicine and clinical genomics, as well as practical experience with bioinformatic tools used for analysis of clinical Next Generation Sequencing (NGS) data.

You are inspired by the promise of this field, but are aware of and critical to the technological, analytical, ethical and organizational barriers hindering its effective implementation. You bring strategic and systems thinking approaches to the table to enable quality assurance and data sharing in this area.

The successful candidate will be a part of a unique multidisciplinary and international research team with the opportunity of influencing DNV GL’s.

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