Location & dates EMBL Heidelberg, Germany 4 - 6 Nov 2019
Deadlines Registration closed Abstract submission closed

Coronavirus information for participants

The onsite course and conference programme at EMBL has been paused until the end of June 2020.


We aim to continue offering our advanced training for the scientific community however we safely can. While some events have been cancelled, many have been rescheduled for a later date and others will be delivered as virtual events.


Registration is open for onsite courses and conferences starting after 1 July and for the virtual events. All registration fees for any events which don’t take place due to the COVID-19 disruption are fully refundable.


More information for participants of events at EMBL Heidelberg can be found here.

Pre-Conference Workshop

The following optional pre-conference workshop will be hosted by the conference sponsor Samplix and will take place before the EMBL Conference: Cancer Genomics

Xdrop™ - Targeted Sequencing enabled into the Dark and Unknown

Date: Monday, 4 November 2019, from 11:30 to 12:30
Venue: Helix Seminar Room A, EMBL Advanced Training Centre

Peter Mouritzen, Ph.D.
VP of Market and Application Development, Samplix ApS

 

Targeted sequencing data will never be better than the input material generated during the targeted enrichment process! While this may seem trivial, very few targeted enrichment technologies allow the user to maintain the integrity and quality of the DNA during enrichment. This results in both false positives and false negative results and can significantly impact conclusions. The Xdrop™ technology, a novel automated microfluidics-based targeted enrichment system, enables fast targeted enrichment while maintaining the quality of the DNA and thus makes it possible to avoid the artefacts introduced with other enrichment technologies. Here we show the Xdrop™ system being employed to sequence integrated viruses and their surrounding unknown chromosomal sequence, sequence long GC repeats, and we show phasing of mutations from sub-nanograms of DNA. Regions of 40-70 kb are enriched and sequenced using Illumina, PacBio, and Oxford Nanopore sequencing at high coverage. Apart from the Xdrop™ reagents, just 0.2-10 ng of input DNA and two adjacent 20-25 bp primers are used for the enrichment of a chromosomal region and it is therefore fast and easy to set up for a new region. The primers are located in the central part of the enriched region which means that partially unknown regions can also be enriched using the system making it relevant for regions with structural variation, CRISPR gene editing, gap closing, variable viruses or bacteria, pseudogenes etc. We also show that the Xdrop™ system can be used for general, unbiased isothermal amplification of small amounts of samples of DNA for any type of downstream sequencing.

All conference participants will receive an email with a registration link. 

Participation in the workshop is first come - first served.