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UPCOMING EVENTS

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Clinical Decision Support-based Reporting: The Power of a Comprehensive Curated Knowledgebase.

 

Date: November 7th 2024

Time: 8 AM PST/ 11 AM EST/ 4 PM GMT

Key takeaways:

Explore what our Knowledgebase has to offer, including everything from relevant therapies, clinical trials, literature, and databases.

Learn how we maintain the highest level of quality in our Knowledgebase that enabled us to power tumor profiling in Illumina’s TSO Comp assay that was recently granted FDA-approval.

Hear about the limitations of IVD-grade reports and how supplemental clinical decision support can help.

Explore how CGW Plus utilizes our best-in-class Knowledgebase to simplify and increase transparency of clinical decisions for laboratories.

videos

On-demand library.

Improving Accuracy and Efficiency Leveraging a Human Pangenome Reference Webinar.
October 24, 2024

Improving Accuracy and Efficiency Leveraging a Human Pangenome Reference Webinar.

What will you learn in this webinar: 

  • Enhanced Genomic Accuracy: See how pangenome references improve equity, scientific rigor, and clinical utility over standard methods.
  • Superior Alignment: Learn how better sequencing read alignment leads to more accurate variant calling, particularly in complex regions like MHC.
  • Efficiency Gains: Understand how these technologies cut computational costs and time, removing the need for expensive joint calling.
watch here
Instagram - Blog FDA LDT (LinkedIn Video Ad)
October 2, 2024
The Variant Interpretation for Cancer Consortium (VICC) - FDA LDT Discussion

Drs. Eric Konnick, Yassmine Akkari, and Andy Bredemeyer discuss the recent decisions and actions surrounding FDA governance of laboratory developed tests (LDTs) - the Final Rule, current lawsuits, and what it all means for those of us in cancer genomics.

watch here
Product Documentation Video (5)
October 3, 2024
Optimizing RCM with 2024 CPT Code Updates.
Explore how the new 2024 CPT codes could impact your organization's reimbursement rates, along with the latest trends in NGS reimbursement and insights into the Medicare Gapfill process. We also discuss how Velsera can help your organization maximize reimbursement and streamline your revenue cycle management workflow.
watch here
Improving Accuracy and Efficiency Leveraging a Human Pangenome Reference Webinar.
October 24, 2024

Improving Accuracy and Efficiency Leveraging a Human Pangenome Reference Webinar.

What will you learn in this webinar: 

  • Enhanced Genomic Accuracy: See how pangenome references improve equity, scientific rigor, and clinical utility over standard methods.
  • Superior Alignment: Learn how better sequencing read alignment leads to more accurate variant calling, particularly in complex regions like MHC.
  • Efficiency Gains: Understand how these technologies cut computational costs and time, removing the need for expensive joint calling.
watch here
Instagram - Blog FDA LDT (LinkedIn Video Ad)
October 2, 2024
The Variant Interpretation for Cancer Consortium (VICC) - FDA LDT Discussion

Drs. Eric Konnick, Yassmine Akkari, and Andy Bredemeyer discuss the recent decisions and actions surrounding FDA governance of laboratory developed tests (LDTs) - the Final Rule, current lawsuits, and what it all means for those of us in cancer genomics.

watch here
Product Documentation Video (5)
October 3, 2024
Optimizing RCM with 2024 CPT Code Updates.
Explore how the new 2024 CPT codes could impact your organization's reimbursement rates, along with the latest trends in NGS reimbursement and insights into the Medicare Gapfill process. We also discuss how Velsera can help your organization maximize reimbursement and streamline your revenue cycle management workflow.
watch here
09/10/2024

Tackling Complexity in Oncology Biomarker Interpretation with CGW Plus.

A discussion of challenges and innovative solutions in clinical genomics workflows. Discover how laboratories leverage variant databases and medical genomics knowledge to automate and...
A discussion of challenges and innovative solutions in clinical genomics workflows. Discover how laboratories leverage variant databases and medical genomics knowledge to automate and...
08/10/2024

RHEO in Action: A snapshot of innovation

Discover how users can effortlessly automate complex bioinformatics analyses with RHEO's push-button solution, designed to handle any use case or data modality. With seamless integration into existing external systems like cloud storage buckets, local databases, and...
Discover how users can effortlessly automate complex bioinformatics analyses with RHEO's push-button solution, designed to handle any use case or data modality. With seamless integration into existing external systems like cloud s...
08/01/2024

Expanding Your Research Horizons: Single Cell and Spatial Transcriptomics Capabilities in Biomedical Research

Discover how single-cell RNA sequencing and spatial transcriptomics are transforming our understanding of tissue cell diversity, developmental...
Discover how single-cell RNA sequencing and spatial transcriptomics are transforming our understanding of tissue cell diversity, developmental...
04/03/2024

Accelerating Drug Discovery: How GRAF Pangenomes Enable Enhanced Insights From Sequencing Data.

Uncover solutions to the pressing challenges in Next-Generation Sequencing (NGS) data analysis with Velsera. Join our upcoming webinar to address a pivotal...
Uncover solutions to the pressing challenges in Next-Generation Sequencing (NGS) data analysis with Velsera. Join our upcoming webinar to address a pivotal...
02/29/2024

State of the Union: NGS Reimbursement

Learn about how the new 2024 CPT codes may impact your organization's reimbursement rates, current trends for NGS reimbursement, the Medicare Gapfill process and more!
Learn about how the new 2024 CPT codes may impact your organization's reimbursement rates, current trends for NGS reimbursement, the Medicare Gapfill process and more!
11/14/2023

High Quality, Automated Oncology ‘Omics Reporting

In this session, we highlight how Velsera’s Knowledgebase powers these insights based on our expert curation of current medical knowledge and clinical trial opportunities.
In this session, we highlight how Velsera’s Knowledgebase powers these insights based on our expert curation of current medical knowledge and clinical trial opportunities.
10/13/2023

Unleashing the Power of Neoantigens

Discover how the identification of neoantigens is opening doors to more effective cancer treatments, as well as the potential for personalized therapeutic strategies.
Discover how the identification of neoantigens is opening doors to more effective cancer treatments, as well as the potential for personalized therapeutic strategies.
10/3/2023

MolDX at a Glance for NGS

This webinar provides information about the following changes and how you can stay reimbursed. Recent policy changes from United Healthcare will significantly impact how organizations are reimbursed for NGS testing.
This webinar provides information about the following changes and how you can stay reimbursed. Recent policy changes from United Healthcare will significantly impact how organizations are reimbursed for NGS testing.
09/21/2023

Comprehensive Clinical Molecular Results Reporting

Velsera’s CGW reveals clinical insights for genomic and other biomarkers in oncology and inherited disease indications, enabling your laboratory staff to rapidly assess, interpret, and report patient management impact to the ordering clinician.
Velsera’s CGW reveals clinical insights for genomic and other biomarkers in oncology and inherited disease indications, enabling your laboratory staff to rapidly assess, interpret, and report patient management impact to the order...
08/29/2023

Multi-Modal Analysis and Imaging for Enhanced Diagnosis and Treatment

Explore the significance of imaging in precision medicine applications and the transition towards integrating ML-AI techniques in multi-modal analysis in the cloud.
Explore the significance of imaging in precision medicine applications and the transition towards integrating ML-AI techniques in multi-modal analysis in the cloud.
07/03/2023

Interpreting the Tumor Genome

How Velsera uses sources of medical knowledge and an understanding of the biology of oncology biomarkers to power the insights you see in the CGW.
How Velsera uses sources of medical knowledge and an understanding of the biology of oncology biomarkers to power the insights you see in the CGW.
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