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Discussing the future of precision medicine.

Level Up your Documentation Processes and Systems to Comply with FDA Final Rule Stages 1 & 2

FDA’s ruling on enforcement of in vitro diagnostic (IVD) medical device requirements for laboratory-developed tests (LDTs) was published in May of 2024. Barring delays from legal or legislative action, enforcement of Stage 1 will begin in 9 months. W...
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Enhancing the Precision Medicine Journey

Five Focus Areas for Our Chief Customer Officer
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Get Ready to Comply with FDA Final Rule Stages 1 & 2: Yeah, We Mean You

FDA's New LDT Rule: An Overview
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Navigating your molecular lab’s test selection and development over the next two years

With the FDA’s publication of the final rule on laboratory developed tests (LDTs) on May 6, 2024, cl...
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Unravelling Cellular Complexity: Exploring 3D Genome Structure and DNA Methylation with the snM3C Pipeline

Understanding the three-dimensional genome architecture is an important feature when analysing gene ...
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Four Years, Five Stages: the FDA's Final Rule on LDTs

After over a decade-long saga, the Food and Drug Administration (FDA) published its final rule on La...
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Making the Most of Multi-Modal Tissue Atlases with Cloud Compute

Why Tissue Atlases? The omics revolution has fundamentally altered our understanding of cellular het...
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Meeting the NIH Data Management and Sharing (DMS) policy requirements

The Velsera suite of NIH-funded platforms including Cancer Genomics Cloud (CGC), BioData Catalyst Po...
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Teaching Introduction to Bioinformatics on the Cancer Genomics Cloud

Velsera is deeply committed to enabling precision medicine not only through accelerating discoveries...
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Highly Customizable Multi-sample Single Cell RNA-Seq Pipeline on CGC

The reasons and rationale behind single-cell RNA-Seq “To study human biology, we must know our cells...
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