Current Press Releases:
For Immediate Release
Contact: Kathy Ridgely Beal, MBA
Media Alert: Complimentary Press Registration is Now Open for the
ACMG 2016 Annual Clinical Genetics Meeting
Health, science and genetics media are invited to register now for the American College of Medical Genetics and Genomics Annual Clinical Genetics Meeting, March 8-12, 2016...
Ambry Genetics (Ambry), a leader in clinical genetic diagnostics and genetics software solutions, announced today that seven abstracts from the company's scientific internal and external collaborative research will be presented at the 2016 American College of Medical Genetics and Genomics (ACMG) Annual Clinical Genetics Meeting taking place March 8-12 in...
Ambry Genetics Shares New Data on Genetic Causes for Neurodevelopmental Conditions, Further Adding to Growing Body of Evidence in Neurology
Oral platform presentation suggests link between KIAA2022 gene mutations and epilepsy, mild to severe intellectual disability, autistic features, and behavioral disturbances in females
Second presentation reveals ASPM gene mutations as likely cause...
BioDiscovery’s Nexus Copy Number software is a leading solution for researchers across the globe for analysis of sequence and structural variation. The software is built on over a decade of research, design, and development in the genomics field and offers unique and user-friendly features to advance research studies.
A cutting-edge feature...
BioDiscovery, Inc. a leader in innovative genomic data analysis software recently released NxClinical 2.1, a comprehensive software solution for molecular genetics and cytogenomics labs. NxClinical is a flexible, platform-agnostic database solution for efficient analysis, interpretation, and reporting of genomic variations and is rapidly being implemented by both hospital and independent...
Analyzing samples from all over the world allows us to constantly expand our unique portfolio. Behind every reported variant there is a clinical case analyzed at CENTOGENE by following a standardized workflow with accredited quality.
CentoMD®2.1 - the world’s largest mutation database of rare diseases. This unique, CE-labeled collection of more...
CentoMD®, the largest genotype-phenotype database for rare diseases
› CentoMD® - CENTOGENE’s mutation database: the vital importance of clinical data
Prof. Peter Bauer, COO, Centogene AG
› CentoMD® in the era of NGS diagnostics and HPO phenotyping
Daniel Trujillano, Phd, Senior Director Bioinformatics, Centogene AG
› CentoMD® - Questions & Answers
Prof. Peter Bauer, COO, Centogene...
Introducing Color's Provider Platform: Bringing Efficiency and Simplicity to Genetic Testing
Color’s mission is to democratize access to genetic testing in a responsible way. A major part of responsible access is ensuring that healthcare providers can easily order Color for their patients, and then understand and engage with their patients’ Color...
Color Genomics Partners with University of California Health System in Landmark Athena WISDOM Study
We are excited to announce that Color has been selected as the genomics partner for the Athena WISDOM Study, a $14.1 million-funded University of California (UC) Health system-wide program in collaboration with Salesforce and Blue Shield of...
Simple and convenient. Those are the words that we use to describe our favorite products in our everyday lives. At Color, one of our top priorities is to build simple and convenient tools for healthcare providers so that they can efficiently get the genetic information they need for their patients.
With a reputation for innovation in pre-analytics, COPAN is a worldwide leading manufacturer of collection and preservation systems for microbiological investigation of infectious diseases and biological samples for genetics and forensic applications. Copan's sample collection devices are designed to maintain chain of custody, facilitate automation, preservation, storage, and enable high...
Call for Research Proposals Issued at the American College of Medical Genetics and Genomics (ACMG) Annual Meeting 2016
FDNA Inc. (Boston, MA) issued today a call to geneticists to submit research proposals to the third cycle of the GIVE A FACE TO A SYNDROME research program. The announcement coincides with the...
BioReference/GeneDX Presentation Slate
at ACMG ‘16
NOTE TO MEDIA: Electronic copies of all GeneDx presentations are available to members of the media by emailing firstname.lastname@example.org. In addition to oral presentations, GeneDx scientists will also make poster presentations over the duration of ACMG16; GeneDx will also be at Booth #418 on the exhibit...
Mawi DNA Technologies is pleased to introduce iSWAB-Blood, a unique new product designed to greatly streamline the collection and processing of blood drops. iSWAB-Blood overcomes issues associated with the use of dried blood spots on filter paper such as insufficient yield, fragmented DNA, potential cross-contamination, and laborious extraction procedures. Using...
Mawi DNA Technologies, a biotechnology company focusing on the development of innovative technologies for biosampling, announces that the US Patent and Trademark Office has issued US Patent No. 9,138,205 for a Sample Recovery and Collection Device.
“The issuance of this patent is a first step towards our vision of providing efficient...
Parabase Genomics is donating two NewbornDx™ tests for families in need. Register to win a NewbornDx™ test for one of your patients. Visit booth #720 to sign up or click here.
This test empowers medical professionals to determine the best possible treatment options within the therapeutic window through early diagnosis.
The NewbornDx™ test:
Hundred of rare genetic...
Take a minute to discover PedigreeXP, the #1 pedigree drawing and managing software and get your free trial!
Make the most of this event to meet with our experts. To plan a meeting ahead, please send us an e-mail at email@example.com or call 00 33 1 69 53 46 20.
We’re at booth...
SciGene (Sunnyvale, CA) has introduced a high capacity system for performing FISH hybridization assays. The system consists of a one CytoBrite Slide Incubation System for performing rapid probe denaturation on batches of 12 FISH slides and one CytoBrite Slide Oven for overnight hybridizations of 60 slides. Removable slide trays streamline...
Manchester, UK and Gentbrugge, Belgium – February 16, 2016 – EMQN, Europe’s leading organization for quality promotion and assessment in Clinical Genetic Testing, and Trinean, provider of microfluidic spectrophotometry platforms, today announced that the DropSense™96 has been integrated by EMQN as the standard QC tool for DNA samples used in...
Gentbrugge, Belgium, January 13 2015 – Trinean, the leading provider of microfluidic spectrophotometry platforms, today announced that its DropSense96TM droplet reader has been chosen by UK Biobank for automated quantification of 500,000 purified DNA samples in its Genotyping project.
UK Biobank’s Genotyping project is one of the largest genetic studies, designed...
WuXi NextCODE and Fudan Children’s Hospital Partner to Lead Whole Genome Diagnostics for Rare Diseases in China
Bringing the world’s leading genomics infrastructure into China’s top pediatric hospital will create national center of excellence for integrated diagnostics, research, treatment and care
SHANGHAI; CAMBRIDGE, Mass.; and REYKJAVIK, 16 September 2015 –...
Genomics England Contracts with WuXi NextCODE as Clinical Interpretation Partner in both Rare Disease and Cancer
LONDON; SHANGHAI; CAMBRIDGE, Mass.; REYKJAVIK, 12 November 2015 – Genomics England has today announced that it has contracted with WuXi NextCODE as a Clinical Interpretation Partner for the 100,000 Genomes Project. The China, US...
Sidra Selects WuXi NextCODE to Power Population Genomics and Precision Medicine in Qatar
In landmark partnership, Sidra Medical and Research Center, the genomics and informatics hub for the Qatar Genome Project, adopts the leading infrastructure for large-scale research and clinical genomics
Whole-genome pilot for 3000 samples using WuXi NextCODE system...
Cancer, Meet the Alamo: San Antonio Enlists WuXi NextCODE to Speed Unparalleled Open-access Cancer Genome Project
World’s leading genomics system to power the first longitudinal study of tumor-normal whole genome data matched in real time with patient progress and outcomes, freely available worldwide
The San Antonio 1000 Cancer Genome Project...
Register will open in October 2016
March 21 - 25, 2017
Phoenix Convention Center
Reserve your room early to get the best choice.
Tweeting about the ACMG Annual Meeting? Use our official hashtag #ACMGMtg16
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