![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
NGS Data Analysis Workshop in Frankfurt, Germany | ecSeq Bioinformatics | Bioinformatics | 0 | 03-28-2017 05:11 AM |
NGS Data Analysis Workshop & Conference: NGS 2017 Glasgow (15-16 May) | Biotexcel | Events / Conferences | 0 | 02-09-2017 11:11 AM |
Upcoming NGS Workshop: A Beginner's Guide to NGS Data Analysis (early march 2015) | ecSeq Bioinformatics | Events / Conferences | 9 | 07-01-2015 01:39 AM |
Upcoming NGS Workshop: A Beginner's Guide to NGS Data Analysis (early march 2015) | ecSeq Bioinformatics | Clinical Sequencing | 1 | 06-29-2015 08:31 AM |
Upcoming NGS Workshop: A Beginner's Guide to NGS Data Analysis (early march 2015) | ecSeq Bioinformatics | Bioinformatics | 1 | 01-15-2015 02:35 AM |
![]() |
|
Thread Tools |
![]() |
#1 |
Member
Location: Manchester, UK Join Date: Jan 2015
Posts: 18
|
![]()
CLINICAL NGS DATA ANALYSIS WORKSHOP, 12th November 2019 at Kennedy Center (Copenhagen)
This workshop will aim to go over the steps from acquisition of sequencing data to the generation of the bam- and vcf- files that will be used in the subsequent filtering for variants. Variants will be evaluated using various databases and prediction tools to establish potential pathogenic variants. Workshop delegates will be given tutorials and examples and will be expected to handle the data themselves on their own laptops under the teacher's guidance. The teachers of this workshop will be from the Bioinformatics team of Odense University Hospital (OUH) led by Prof Klaus Brusgaard. This workshop is part of the Genomic Medicine 2019 Nordic conference. Please contact us if you would like to book the workshop only. Last edited by Biotexcel; 08-02-2019 at 05:36 AM. Reason: More information added |
![]() |
![]() |
![]() |
Tags |
bioinformatics, clinical bioinformatics, data analysis, sequecing, variant interpretation |
Thread Tools | |
|
|