At ACMG 2025, Dr. Moez Dawood announced a groundbreaking initiative: the global democratization of deidentified allele count and frequency data…
Blog Post
As a part of our ongoing effort to update our variant effect predictors with calibration for ACMG/AMP classifications, we have…
On the final day of OpenCRAVAT’s Adventurer’s Guide, we celebrate you—our community. OpenCRAVAT thrives because of the passion, creativity, and…
On the 11th day of OpenCRAVAT, we’re diving into a standout feature: widgets. Widgets transform data into interactive visualizations and…
As we approach the end of our 12 Days of OpenCRAVAT, let’s dive into how the OpenCRAVAT API can revolutionize…
Cloud computing has transformed genomic variant analysis by enabling scalable and accessible workflows. With OpenCRAVAT, you can run your analyses…
Computational methods for predicting the effects of genetic variants are used by clinicians for interpreting genetic test results and by…
Efficient data filtering is critical to making sense of your analysis. OpenCRAVAT offers eight customizable filtering options to help you…
OpenCRAVAT is designed with flexibility in mind, offering users the ability to tailor their genomic variant analyses to specific research…
On the sixth day of OpenCRAVAT, we’re highlighting six essential tools that transform your genomic data into actionable insights. These…