Genomics researchers use different sequencing techniques to better understand biological systems, including single-cell and spatial omics. Unlike single-cell, which looks at data at the cellular level, spatial omics considers where that data is located and takes into account the spatial context for analysis. As genomics researchers look to model biological systems across multiple omics at…
]]>NVIDIA Parabricks v4.3 was released at NVIDIA GTC 2024, introducing new tooling and workflows that bring acceleration and the latest AI techniques to multiple omics data types. In addition to analyzing DNA and RNA, you can now also analyze methylation, single-cell, and spatial omics workloads at high speed and high accuracy with the power of GPUs and generative AI. Parabricks v4.3…
]]>NVIDIA BioNeMo Framework has been released and is now generally available to download on NGC, enabling researchers to build and deploy generative AI, large language models (LLMs), and foundation models in drug discovery applications. The BioNeMo platform includes managed services, API endpoints, and training frameworks to simplify, accelerate, and scale generative AI for drug discovery.
]]>Parabricks version 4.2 has been released, furthering its mission to deliver unprecedented speed, cost-effectiveness, and accuracy in genomics sequencing analysis. The latest version delivers a newly accelerated workflow for Oxford Nanopore sequencing (in the featured image), enables Parabricks to be run on the latest NVIDIA GPUs, and furthers Parabricks’ accelerated deep learning variant calling…
]]>The human exome is key to understanding and treating genetic disorders and disease. Although the exome consists of just over 1% of the human genome, it also contains approximately 85% of known variants with significant disease-associated mutations. This is why whole-exome sequencing, involving the extraction and sequencing of these regions, is popular in clinical research and practice…
]]>The upcoming 4.1 release of NVIDIA Parabricks, a suite of accelerated genomic analysis applications, goes further than ever before in accelerating sequencing alignment and increasing the accuracy of deep learning variant calling. The release includes a new workflow for PacBio long-read data, featuring an accelerated Minimap2 tool and Google’s DeepVariant for full GPU-enabled, end-to-end analysis…
]]>The field of computational biology relies on bioinformatics tools that are fast, accurate, and easy to use. As next-generation sequencing (NGS) is becoming faster and less costly, a data deluge is emerging, and there is an ever-growing need for accessible, high-throughput, industry-standard analysis. At GTC 2022, we announced the release of NVIDIA Clara Parabricks v4.0…
]]>Fast and cost-effective whole genome sequencing and analysis can bring answers quickly to critically ill patients suffering from rare or undiagnosed diseases. Recent advances in accelerated clinical sequencing, such as the world-record-setting DNA sequencing technique for rapid diagnosis, are bringing us one step closer to same-day, whole-genome genetic diagnosis in a clinical setting.
]]>