Travel time is approximately minutes. Taxis are available 24h in front of all terminals. The airport is just a five-minute walk from the railway station via a covered walkway.
Travel time is approximately 60 minutes. Tickets can be purchased online or at any of the vending machines in the station. For more information on tickets, zone maps and route planners visit the BVB website. A total of 12, parking spaces are available on and around the grounds. Please see here for an overview map.
6-9 June 2020 | ESHG 2020.2 – Live in your living room
Be aware of the Environmental Zone: The Environmental Zone is the area within the so-called S-Bahn ring, the light railway line encircling central Berlin. Vehicles may only enter this area if they display a valid sticker showing that their emissions do not exceed a specified level of fine particulates.
Road signs clearly indicate where this Environmental Zone begins. Although the southern section of the city expressway, the Stadtautobahn, is within the S-Bahn ring, it is not classified as part of the Environmental Zone because it is also used to enable vehicles to drive around the restricted area. The CityCube is located outside the Environmental Zone. The public transport system is operated by BVB Berliner Verkehrsbetriebe and offers an extensive network of metro lines, light railways lines, regional trains, express busses and night busses.
For further information on timetables, maps, ticket prices and route planners, please visit the BVB website. The German capital is a melting pot of ideas and innovation; a city of diversity, contrasts and a vibrant creative metropolis.
Regarded worldwide as a leading destination for events and conferences, Berlin sets a benchmark for high standards, service and unique experiences. Berlin has an eventful history, a pulsating lifestyle, and has reinvented itself as a cosmopolitan city with a unique flair. Open-minded and intriguing, multi-cultural and multi-lingual, but also with an outstanding infrastructure; Berlin has continued to evolve at a pace unmatched by almost any other city since German unification.
Its rich cultural offering includes approximately museums and historical monuments, a thriving international art scene portrayed in more than galleries, no less than three UNESCO World Heritage sites and an array of trendy shopping districts. When it comes to dining, Berlin has every taste covered with a diverse culinary offering from the humble Currywurst, kebab, and meatballs to extravagant Michelin-starred experiences, flexible creative catering, and fashionable street food; including delicious and authentic vegan, organic, kosher and halal dishes.
Check this website from Visit Berlin for more information and tips on places to go, eat and shop in the city. Search for:. How to reach the venue? Berlin Welcome to the City of Freedom — from walled city to world city!
If you continue to use this site we will assume that you are happy with it. Ok Read more.At ESHGBlueprint Genetics presented multiple posters, in-booth talks and held a corporate satellite session on difficult-to-sequence regions and high resolution CNV detection. Planning for the upcoming ESHG has already started, so stay tuned for the updates! We are looking forward for ESHG to meet you again. We have already confirmed our well attended Corporate Satellite for ESHG and it will be on the familiar slot during the Saturday lunch break.
Please be advised that we only accept specimen collection kit requests from medical professionals. If you are a patient or family member of a patient, please contact your provider to place a kit order on your behalf.Ramal İsrafilov - Eşq 2019 (Official Audio)
Blueprint Genetics. Diagnostic tests Menu Diagnostic tests. Menu Testing with us. Pricing Pricing. Menu Technology. Accessibility Nucleus Connecting Clinicians. Menu About us. Newsroom News. Meet Us Events. Menu Resources. Education Webinars White papers. Subscribe to our newsletter. Last modified: Deliver kit to patient Deliver kit to patient. Phone number.
Delivery address line 2. Number of Blood Kits. Number of Saliva Kits. Number of Exome Kits. My Retina Tracker Blood Kits. My Retina Tracker Saliva Kit. Other Information.At the ESHG meeting, we thrive to bring you what is at the forefront of human genetics both scientifically and technologically without losing sight of educating the upcoming generation of human geneticists. It invites the best speakers for the concurrent symposia and selects the best abstracts for oral presentations during the concurrent sessions to create a program that represents the breadth of our specialty.
These presentations are completed by a set of educational sessions given by invited speakers and which are aimed to update you on various topics in genetics. Our meeting would not be complete without our exhibitors who advertise their new products to help you in your clinic, your diagnostic laboratory and your experimental work. I am particularly pleased to see that year after year many young human geneticists present their results and compete for our multiple young investigators awards.
Their enthusiasm and passion when they take the stage is an integral part of the ESHG meeting. Booth: Event category: Conferences. Type of Event: Conference. Admission: Public. ESHG Thu 6th June - Mon 10th June Berlin, Germany At the ESHG meeting, we thrive to bring you what is at the forefront of human genetics both scientifically and technologically without losing sight of educating the upcoming generation of human geneticists.
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Search Search. Nanopore Search Search content across Nanopore Filter results by content type to refine searches and explore areas of interest. Most relevant Newest Oldest.Click here for information on upcoming Board Meetings. Click here for information on nomination procedures and task descriptions for new Board Members and President. Members who wish to raise issues for discussion at the Board should contact the Secretary-general or a member of the Board, whose members are shown below.
Term as board member ends at the general assembly in the year given in the according column. Gunnar Houge. Click here for information on nomination procedures and task descriptions for new Board Members and President Members who wish to raise issues for discussion at the Board should contact the Secretary-general or a member of the Board, whose members are shown below.
Carla Oliveira Porto Treasurer Prof. Ana Beleza Bristol Dr. Marta Bertoli Newcastle-upon-Tyne Prof. Olaf Bodamer Boston Prof. Jill Clayton-Smith Manchester Prof.
Meeting Calendar 2020
Johan den Dunnen Leiden Prof. Josef Gecz Adelaide Dr. Christian Gilissen Nijmegen Dr. Kinga Hadzsiev Pecz Dr. Ellen Heitzer Graz Prof. Robert Hofstra Rotterdam Prof. Bart L. Loeys Antwerp Dr. Christine Patch London Prof. Christina Rusu Iasi Dr. Sergio Sousa Coimbra Prof. Birute Tumiene Vilnius Dr. Laura Valle Barcelona Prof. Hilde Van Esch Leuven Dr. Reiner A. Veitia Paris Dr.
Kirmo Wartiovaara Helsinki Term ends. Milan Macek Jr. GertJan B. Alexandre Reymond. Maurizio Genuardi. Karin Writzl. Carla Oliveira. Andrew Read.Although exome sequencing is now routinely available both for research and clinical purposes, the interpretation of identified variants remains a major challenge. In this workshop, we will discuss publicly available resources to aid in variant interpretation from exome sequencing, methods to make the most of exome sequencing data, and lessons learned as part of theGenomes Project.
We will finish with real-life examples from clinical cases.
The highs and lows of whole genome sequencing for rare and inherited disorders in theGenomes Project 15 minutes Ellen Thomas. With this in mind, we propose a method of allowing clinicians to access this information promptly to benefit patients affected by rare disease and their families.
By including speakers with both a research and practical focus on genetic counselling and test delivery, we also aim to illuminate multiple approaches to addressing these. We will encourage critical analysis and discussion of these approaches to gain understanding of their effectiveness and replicability.
On-demand Sessions. Search for:. Please note that all live sessions will be available on-demand the next day. Welcome to ESHG View an outline of highlights of the day presented by an SPC member. E03 Pharmacogenomics in the Clinic.
E04 Hypermobility and the Ehlers Danlos Syndromes. E06 Brain Size Matters! Mancini ; The Netherlands E E08 Does Genetic Counselling Work? E09 Updates on Mitochondria Diagnostics. E10 Therapy for Rare Disorders. E11 Heritability Estimations.
E12 Artificial Intelligence in Biomedicine. E13 Mainstreaming Mitochondrial Replacement Techniques? Lockhart ; Australia E Tabrizi ; United Kingdom. More information soon. W02 Exome and Genome Variant Interpretation. Workshop Organiser: Kaitlin Samocha About the workshop: Although exome sequencing is now routinely available both for research and clinical purposes, the interpretation of identified variants remains a major challenge. W04 Pharmacogenomics in Practice. Live Sessions.Samplix will be attending - and presenting - at the Genome Editing conference on March To see the conference agenda and register for the event, please visit the conference website.
To see more and register for the event, please visit the conference website. Samplix is pleased to announce we will be attending the Genomic Medicine Nordic conference 13 - 14 November at Kennedy Center at Rigshospitalet in Copenhagen.
Scientists in the genomics field can now routinely capture up to kb long genomic regions, based upon very limited target sequence information bp of sequence. January The selection process was highly competitive with more than 1.
All rights reserved. For Research Use Only. Not for use in diagnostic procedures.
To read more, please see the full press release here:. Read more. Need more information? Contact us. Contact Mileparken 28 Herlev Denmark info samplix. Connect with us. Log ud.If you have not received any notifcation, please contact us at conference eshg. We can confirm that despite the translation to a virtual conferenceyour a bstract acceptance still applies and we would appreciate if your original commitment to present your research can be upheld in a virtual form.
We will contact you with further information on the technical side of this new and exciting format as soon as possible. We kindly ask all submitters to check their e-mails for further notifications on a regular basis. All applications made through the online abstract submission have been reviewed. Applicants will be informed about their application by e-mail until April 20, All fellowship holders will receive free registration to attend the ESHG Late Breaking Abstract Submission will be open from May The Programme Committee will consider a maximum of 6 abstracts being expected to have a major impact in the field.
All abstracts are peer-reviewed and ranked on the basis of scientific merit by experts in the category selected. The Scientific Program Committee uses these rankings to develop the scientific sessions.
Abstracts are assigned to either plenary, parallel, or poster sessions. Abstracts considered to be of particular interest to the media may be selected for press release. Please note that, once work has been published, it cannot be considered as a candidate for a press release. The enormous achievements in the field of Human Genetics during the last years are changing not only our understanding of genetics of diseases but also our research approaches and daily work in clinic.
Due to the new developments and insights traditional borders between clinical genetics, cytogenetics and molecular genetics as well as between research into monogenic and complex disorders are vanishing.
Therefore the Scientific Programme Committee of the European Society of Human Genetics decided to reflect these changes in its abstract submission categories. The disease categories as well as 12 are meant to cover all aspects of the specific disorders indicated, i.
Topic 13 is meant for abstracts discussing genomic variation and genome structure not necessarily related to a specific phenotype e. Topic 15 shall draw attention to brand new concepts or new genomic technologies and the evaluation of their potential. Topic 16 is dedicated to general aspects of technical approaches and quality control in genetic diagnostics and research.
Topic 17 is dedicated to abstracts related to bioinformatics and statistical approaches in genomics. Topic 18 is meant for abstracts studying the role of genomics to personalize medicine, including but not limited to the application of pharmacogenomics. Topic 19 is meant for abstracts in genetic epidemiology, population genetics and evolutionary genetics. Topic 20 is for abstracts dedicated to epigenetic studies and functional genomic studies. Topic 21 is for abstracts related to novel therapeutic opportunities for genetic disorders.
EMPAG has now become an integral and yearly part of the programme, and covers general issues of genetic counselling, education and public services, psychological, ethical and legal issues. We hope that these categories will enhance the communication between researchers using different approaches to investigate the respective phenotypic groups and facilitate the selection of workshops by attendees according to their field of interest.
Sensory Disorders Eye, Ear, Pain Cardiovascular Disorders Metabolic and Mitochondrial Disorders Immunology and Hematopoietic System Intellectual Disability Neurogenetic and Psychiatric Disorders Neuromuscular Disorders Cancer Genetics Genome Variation and Architecture