Advertisement

Picture Berlin Partner Bionnale 2021 Digital Event 650x80px
Document › Details

Diploid. (6/21/16). "Press Release: InHelix – Next Generation Software for CNV Interpretation". Leuven.

Organisation Organisation Diploid (BE)
Products Product InHelix software for CNV interpretation
  Product 2 genomics
Persons Person Kint, Cyrielle (Diploid 201606 CSO)
  Person 2 Schols, Peter (Diploid 201509 CEO + Founder)
     


Diploid today announces the release of InHelix, software for annotating, visualising, filtering and reporting copy number variants (CNVs) obtained from NGS data. The software has been specifically designed for CNV analysis in rare disease diagnostics.

"CNV analysis has traditionally been carried out using array-based techniques, yielding tens or hundreds of CNVs", says Dr. Cyrielle Kint, Diploid’s CSO. "However, CNV analysis is now increasingly being performed on NGS data, resulting in the detection of about 7,000 CNVs in a single human genome, thousands more than would be detected using a routine array-CGH analysis. InHelix is the first CNV analysis software that has been designed from the ground up to handle the large amount of data generated by genome-wide NGS-based CNV detection. This allows InHelix to offer live filtering and smart ranking of CNVs, quickly guiding geneticists to the most relevant CNVs for a particular case."

InHelix sports a list of other unique features, such as the ability to run a CNV family analysis, leveraging the availability of NGS data from healthy family members to assist in filtering CNVs. InHelix also features innovative SmartPanels™: unique panels generated by InHelix which are based on HPO terms. In order to enable SmartPanels, InHelix mines the literature on a weekly basis, automatically adding new gene-phenotype correlations to the system. As well as SmartPanels, InHelix also features over 80 built-in gene panels manually curated by Diploid's geneticists. In addition, the software enables shortlisting of relevant CNVs and the easy generation of a PDF report. InHelix can import CNV data from callers such as CNVnator, Pindel, CoNIFER, CoNVaDING, Canvas, CNVkit, Control-FREEC and many others.

"We think that InHelix offers a great opportunity for undiagnosed rare disease patients" says Dr. Peter Schols, Diploid's CEO. "Geneticists can call CNVs on pre-existing WGS data - or even WES data - from undiagnosed patients, using InHelix to easily filter and report clinically relevant CNVs, providing a diagnosis for more patients."

InHelix is available as a cloud-based service. It runs on ISO 27001 certified infrastructure and is HIPAA compliant. On-site deployment is possible for larger hospitals and labs, or for nationwide genome projects.

Interested geneticists can create a free online account and will receive 5 complimentary analyses, allowing them to use the platform with their own data. More information is available on the InHelix website, including a 10 minute demonstration movie of the software.


Links
Website: http://www.diploid.com/inhelix

Press Contact
Dr. Peter Schols
pr@diploid.com
http://www.diploid.com
+1 855-855-6501 (US toll free number)

   
Record changed: 2016-07-23

Advertisement

Picture EBD Group Connector Personal Networking in Life Sciences 650x80

More documents for Diploid (BE)


To subscribe to our free, monthly newsletter for the European life sciences, please send an e-mail to info@iito.de and simply fill the subject line with the word »LSE Newsletter«

To get even more information, please take a look at our [gs] professional services offering and read the gene-sensor Product Flyer [PDF file]

Advertisement

Picture [iito] Back into Ad 650x80px




» top