BioDiscovery

Current tools for assessing HRD status are limited to targeted detection of point mutations in HR genes predicted to be causative of HRD or cannot detect abnormalities across the entire genome. NxClinical software can help resolve this limitation by providing a genome-wide scarring approach coupled with integrated SNV analysis of HR genes that may reveal critical insights to tumor biology.

Read more in our latest white paper.

https://hubs.ly/Q01bMqBC0

Our team is growing! Bionano Genomics, Inc. is dedicated to transforming the way the world sees the genome. If you are creative, results-oriented, and enjoy being part of an interdisciplinary team that values extraordinary achievement – Apply Online Today!
https://hubs.ly/Q014JCMw0

In an October 2021 article published in The Journal of Molecular Medicine, members of an Association for Molecular Pathology working group focused on electronic health record (EHR) interoperability for clinical genomics data detailed many of the issues with institutions not having a place to store variant data, stating, “[t]he single most important architectural component that would facilitate the use of genomic data in EHRs is precisely what most, if not all, EHRs lack: the ability to consume and store individual variants discretely in the database in a scalable, standardized, and reliable way.”

The newest version of NxClinical fills this critical role and is a first-of-its-kind database, with its integrated Knowledgebase (KB) module. Read more about how the KB can efficiently organize your genomic variant data.

A first-of-its-kind clinical research genetics knowledgebase: Accelerate your case review with NxClinical: https://hubs.ly/Q013rNFL0

In our latest blog update, we compare the similarities and differences in CNV detection between WES and SNP microarray methods. Read now to learn more about these technologies and the standards being utilized for CNV calling in genomics labs across the world.

Comparison of CNV Detection from WES vs. SNP Microarray https://hubs.ly/Q011XSZl0

Calling all BioDiscovery customers 📣

Do you have a new or previously submitted poster that highlights the use of BioDiscovery software (NxClinical or Nexus Copy Number)? If so, submit it today to the upcoming Bionano Genomics, Inc. 2022 Symposium and share your work with a global audience, plus get a chance to win prizes!

https://hubs.ly/Q01133mF0

In response to valued NxClinical customer feedback, an upgraded version of the software is available now to help you detect, display and decide.

Bionano Genomics Announces the Launch of Version 6.1 of BioDiscovery’s NxClinical Software https://hubs.ly/Q010WLsk0

New learning opportunity alert for those in 🚨

Copy number variants (CNVs) and profiles have both demonstrated immense clinical utility in the molecular diagnosis of many cancers. From the basics of a somatic CNV biomarker to a genome-wide CN signature, read our latest offering on how labs are harnessing their diagnostic and prognostic power to improve patient care.

Cancer Copy Number Variants (CNVs): A Guide for Clinical Researchers https://hubs.ly/Q010mqfs0

Let's see it live, in action, and used by those in the field who are putting it to good use! 🎬
Join us for next week's webinar, presented by Amber Boys of VCGS, where she will highlight clinical case reviews using the new ACMG scoreboard in NxClinical, with details on how this new feature enabled her team to improve the speed and traceability of their curation while being compliant with the latest technical standards.

Rapid implementation of the latest technical standards with the NxClinical integrated ACMG scoreboard https://hubs.ly/H0_HwkW0

BAM! Did you check your reads? If you did, you would have found a nesting pathogenic homozygous deletion!!!

Learn more about how WGS has helped Fen Guo and her team at PerkinElmer Applied Genomics to solve this case and 3 more on rare disorders. Get some insights on how clarity, coverage, and resolution are achieved in detecting copy number variants by NGS with NxClinical.

Copy Number Variant Detection by NGS: Coverage, Uniformity & Resolution https://hubs.ly/H0_xmVK0