Inocras

Very excited to be presenting at #AACR25 our whole genome MRD assay! Stop by our booth (3340) to learn more and learn about our special promotional offer for MRD.

Whole genome testing with actionable insights can help you find a diagnosis. Learn more about RareVision to help get more answers on your symptoms. Use code WELCOME40OFF on your next order! portal.inocras.com/register/?prod… #biotech #genetictesting #rarediseasetesting #rarevision

The National Society of Genetic Counselors meeting starts tomorrow! Stop by and visit us at booth #335. We hope to see you there!

We're gearing up for NSCG! Join us from September 17-21 to learn more about key advancements in genetic counseling to provide education and better serve patients and build community. We hope to see you there! Learn more. nsgc.org/conference

The AGBT Precision Health Conference is next week! Stop by and visit us at booth #207 and learn alongside amazing innovators in biotechnology and healthcare. agbt.org/events/precisi… #AGBT2024 #precisionhealth #genomicinnovation #genomics #biotech

Dr. Erin Connolly-Strong and Dr. Islam Oguz Tuncay will be presenting their respective posters at the upcoming AGBT Precision Health Conference! Stop by and see us at booth #207! #AGBT2024 #precisionhealth #genomicinnovation #genomics #biotech

We're excited to be attending the AGBT Precision Health Conference from September 4th to September 6th! To register and see the agenda, click here. agbt.org/events/precisi…

Our digital ordering platform makes it easy for patients to access comprehensive genetic testing, and get easy-to-understand result reports, actionable findings, genetic counseling support and clinical trial matching. Walking with them through every step inocras.com/get-started/

With over 30 collaborative research studies in partnership with academia and pharmaceutical partners, we are advancing the world’s understanding of genomic science, all with one main goal: improving patient health. #genetictesting #genetics #cancer inocras.com

Fast turnaround times, flexible output file formats and WGS coverage. Additionally, we accept a variety of sample types including gDNA, saliva, whole blood, fresh frozen tissue, and FFPE. Send us a DM to connect. #geneticresearch

Have you been diagnosed with solid tumor cancer? Are you looking for more answers about your symptoms or a clear diagnosis? Our whole genome genetic tests may be able to support you in your health journey. Learn more about CancerVision and RareVision - inocras.com/get-started/

RareVision is a whole genome sequencing test for patients who are looking for a clearer diagnosis or answers. Learn more about RareVision whole genome testing and how you can order the test for your patients. #genetictesting #rarediseasegenetictesting inocras.com/rare-provider/

We want to be your trusted WGS lab partner. Send us an inquiry at inquiry@inocras.com to learn more about our research services. #wgs #wholegenomesequencing #bioinformatics #CLIAlab #geneticresearch #genomics #DNAsequencing inocras.com/researchers/

@WatchmakerGeno1 DNA Library Prep Kit with Fragmentation is the backbone of our assay, and we're thrilled to partner them! Read more about this exciting collaboration as we forge the future of genomic innovation 🧬businesswire.com/news/home/2024…

Are you looking for more answers about your symptoms or help getting to a diagnosis? RareVision can help you learn more about your genes to determine how they may be impacting your health. Learn more and use code LAUNCHPROMO30 for 30% off your test before July 31.

CancerVision is a whole genome test that unveils a comprehensive picture of your genome to help you learn more about your cancer and explore treatment options. Learn more about CancerVision and get 30% off of your test order through July 31 with code LAUNCHPROMO30.

The #MENA Congress for Rare Diseases starts this week! Stop by our booth to meet our team and attend our presentation on identifying complex genetic mutations with whole genome sequencing for the advancement of rare disease detection. We look forward to seeing you!

The MENA Congress for Rare Diseases begins next week! Join us as Dr. Erin Connolly-Strong presents on uncovering previously undetected, complex genetic mutations with whole genome sequencing. For more information and to view the agenda, visit menararediseases.com. #MENA2024

We're excited to present at AACR 2024 Annual Meeting! Our research demonstrates how machine learning helps overcome issues with distorted genomic profiles in FFPE tissues, enhancing the accuracy and reliability of genomic analysis. abstractsonline.com/pp8/#!/20272/p… #AACR2024 #INOCRAS

Welcome to Inocras!🥳