Next Generation Sequencing in Human Health and Translational Medicine

[Paul Butler]

Meeting focused on the NGS Sample preparation workflow. Free to attend. Aula Medica, Karolinska Institute, Conference room 507, Nobels väg 6,171 65 Stockholm, 1st November 2016. Organized by PerkinElmer

AGENDA
10:00 Welcome and Registration Louise Hebert, PerkinElmer
10:10 Solutions for the NGS Workflow Paul Butler, PerkinElmer
10:35 KI Biobank DNA Services James Thompson, KI Institute
11:10 First experiences and future plans for our Sciclone NGSx Morten Skage, Norwegian Sequencing Centre, UiO(University of Oslo
11:40 Use Less, Get More – New Ultra Sensitivity
Assay for LabChip® GX Touch: HT DNA NGS 3K Ilse Villman, PerkinElmer
12:10 Lunch and Laboratory Tours
13:15 Genomics-empowered healthcare: how next generation sequencing is transforming clinical work Pawel Zajac, Illumina
13:45 Applying NGS to clinical diagnostic and research at MOMA Jakob Hedegaard, MOMA, Aarhus, Denmark
14:15 TBA TBA
14:45 Coffee
15:15 PerkinElmer Informatics: Getting Answers from Big Data in Precision Medicine Simone Sharma, PerkinElmer
15:45 Exomes, copy-number and RNA-seq in a cancer genomics core facility James Hadfield, Head of Genomics at CRUK Cambridge Institute
16:15 Questions, Wrap up and Meeting Close

Register at - https://www.eventbrite.co.uk/e/ngs-i...on-27302260797