Ultima Genomics’ Post

A data science roadmap for open science organizations engaged in early-stage drug discovery A nice report by The Structural Genomics Consortium (SGC) working group outlines key strategies to accelerate scientific discovery. It highlights the importance of standardized data management and open collaboration between data scientists and experimentalists. Standardization and automation will enable real-time data integration and analysis, leading to faster development of new drugs and chemical probes. #Science #MachineLearning #Collaboration #openscience

Explore the LATEST 3x3x3 Challenges like this one on Fore Genomics and make sure to check out the most watched 3x3x3 Challenges for July 2024 at BenefitsAlly.com!

The 1st NovaSeq X Plus right here in the heartlands of #SoutheastAsia!  See how we're bringing greater access to genomics services and discover the exciting capabilities the #NovaSeqXPlus offers to researchers. Our journey is just getting started.   Watch what Thomas Neo at Illumina and Justin Lee at Novogene AMEA (APAC, Middle-East & Africa) have to say. https://lnkd.in/gxyGcPHj

Mapping variant effects for a healthier future! Explore the Atlas of Variant Effects Alliance's 2023 Annual Report. From membership growth to global collaborations, discover how we're advancing genomics and making a difference. https://lnkd.in/gxweq3wq

Curious about what it's like to work with us? Listen as Genomenon, Inc, a genomics intelligence company, talks about the benefits of their association with NashBio. 🧬 Watch the full video here: https://hubs.li/Q02Jr1-M0

Explore the LATEST 3x3x3 Challenges like this one on Fore Genomics and make sure to check out the most watched 3x3x3 Challenges for July 2024 at BenefitsAlly.com!

DISGENET — our gene-disease association knowledge platform — was created in 2010. The need for reliable, high-quality genomics data hasn’t faltered, but the way we access data has vastly changed. Which is why the DISGENET platform has undergone a rebrand. We are proud to share the meaning behind our new logo ✨ The DISGENET logo features an elegant “s” shape, reflecting how we support you in transforming complex data into easy-to-understand insights inside our platform. It mirrors our heritage in genomics too, resembling a DNA strand 🧬 What do you think? 👉🏼 Follow DISGENET to learn more about the world’s most extensive and reliable gene-disease association network.

Within the #PublicHealthGenetics and Genomics system, individuals and organizations work to build tools and resources to help support said system. Download today's fact sheet on the #PHGW website to explore select resources. https://lnkd.in/grkvJCCJ #PublicHealthGenomics

GDC 2.0 centers around the idea of building cohorts, or custom groups of cases for genomic analysis. Use the Cohort Builder tool to create and modify cohorts, import and export cohorts, and load cohorts for analysis using the GDC’s other tools https://buff.ly/3OGTHAC #NCIGDC #ResearchDiscovery

Want to learn about #3Dgenomics? #ProximityLigation? This webinar will provide an introduction to 3D Genomics and cover: ~ What Role Does It Play? ~ How Is It Studied? ~ How Is The Data Visualized? ~ Case Studies ~ Accessing 3D Genomics Through Dovetail® Assays ~ The Dovetail® Difference https://lnkd.in/eq9xPTqG