Meetings/Workshops on Medicine (in general) in Sweden

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1
NGS Workshop 2017 Nordic — NGS Data Analysis Workshop - Genomic Medicine 2017 Nordic
07 Nov 2017 • Lund, Sweden
Abstract:
The NGS Data Analysis Workshop 2017 in Sweden is led by Genome Diagnostics Nijmegen. It is held on the 7th November at Lund University, Sweden. The course will be useful for people who are not too experienced in data-analysis but have already some knowledge about NGS. The course will start by providing a good overview of the raw sequencing data, an explanation about the formats and how delegates can check the quality of the data. Following on from this and during the NGS Diagnostics interpretation sections delegates will learn how to work with the analyzed data, how they should interpret the data and how to prioritize the variants to look for the interesting ones. At the conclusion of the course, delegates will be asked to solve diagnostic patient cases by searching for the pathogenic variant(s).
Contact:
Biotexcel;     Email: genmednordic@biotexcel.com
Topics:
Genomics, Genetics, NGS, Next Generation Sequencing, Bioinformatics, Clinical Genetics, Oncology, Cancer, Clinical Genomics, Molecular Biology, Data Analysis, Human Genetics, Biomarkers, Data Storage, Rare Disease, Micro RNA, Circulating Tumour DNA, Cfdna, Mirna, Epigenetics, Transcriptomics, Oncogenomics, Microbiome, Metagenomics, NGS Data Analysis, Personalized Medicine, Diagnostics, Infectious And Inherited Diseases, Molecular Diagnostics
Event listing ID:
911465
Related subject(s):
2
Nordic 2017 — Genomic Medicine 2017 Nordic Conference
08 Nov 2017 - 09 Nov 2017 • Lund, Sweden
Abstract:
Genomic Medicine 2017 Nordic is the fourth annual conference and will take place at Medicon Village in Lund on the 8th and 9th November. The conference will focus on the use of Genomics & Next Generation Sequencing (NGS) technologies and tools to look at human disease whether in a research or a clinical setting. We will cover the following areas: Genomics, Next Generation Sequencing Applications and Workflows, Personalized Genomics, the Metagenomics link to health/disease, Non-invasive Prenatal testing (NIPT), Cancer and Rare Disease genetics as well as Data Analysis and Storage.
Contact:
Biotexcel;     Email: genmednordic@biotexcel.com
Topics:
Genomics, Genetics, NGS, Next Generation Sequencing, Bioinformatics, Clinical Genetics, Oncology, Cancer, Clinical Genomics, Molecular Biology, Data Analysis, Human Genetics, Biomarkers, Data Storage, Rare Disease, Micro RNA, Circulating Tumour DNA, Cfdna, Mirna, Epigenetics, Transcriptomics, Oncogenomics, Microbiome, Metagenomics, NGS Data Analysis, Personalized Medicine, Diagnostics, Infectious And Inherited Diseases, Molecular Diagnostics
Event listing ID:
911477
Related subject(s):

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Last updated: 04 June 2017