A @velsera project enabling cancer multiomics research at petabyte scale.

Joined November 2014
CancerGenomicsCloud retweeted
Bioinformatics’ growth leads to the recognition of its value in healthcare. Can a condensed intro course teach students authentic analysis? Prof. Jeremy Chien taught 14 first-year biology students cancer genomics using CGC. Learn more: sevenbridges.com/teaching-in…
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CancerGenomicsCloud retweeted
Great success for our Velsera sales team and science experts at #AACR23 Engaging with potential clients, presenting talks and posters, and showcasing our solutions for precision R&D, global omics, and insights. #AACR23 #CancerResearch #EraofVelsera
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CancerGenomicsCloud retweeted
IT'S WORLD PANCREATIC CANCER DAY! Let's turn the world purple today! 🎗️📣🗣 Here's how you can join in: 💜 Put on your best purple! 📷 Take a picture (or 2 or 3)! 🏷️ Tag @PanCAN and #PanCANawareness It takes all of us together to raise awareness for #pancreaticcancer! 💜
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CancerGenomicsCloud retweeted
What a tour-de-force review of the biology, genomics, research ecosystem, and development of promising treatments for Neurofibromatoses (NF) by @brkorf at #CGCAnnual2022
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Welcoming our keynote speaker at #CGCAnnual2022 Dr. Bruce Korf @brkorf explaining the genomics of #neurofibromatosis through his lenses of years of experience. For LGG board exam takers, I highly recommend checking out Dr Korf’s lectures! @CG_Consortium #cancergenomics
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CancerGenomicsCloud retweeted
"Bioinformatics tools developed to support BioCompute Objects" New #BioComputeObject Tools paper in @biocurator's #openaccess journal Database discussing #BCO on Cloud-based platforms: HIVE, Cancer Genomics Cloud (CGC) and @galaxyproject , academic.oup.com/database/ar… #BioCompute
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CancerGenomicsCloud retweeted
The first of many CWL-BCOs are under development! Check back here for updates and examples that incorporate BCO with #CommonWorkflowLanguage #CWL
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CancerGenomicsCloud retweeted
In 1997, Prince Hitachi—the younger brother of the Japanese Emperor and a cancer researcher—met with @theNCI scientist Dr. Ira Pastan, who had collaborated with colleagues in Japan.
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CancerGenomicsCloud retweeted
webinar starting in about an hour, slides definitely ready ;)
Happy to share my "human learning" talk on Tuesday. Will briefly cover challenges in training data scientists (& bioinformaticians); how we've leveraged NIH-funded platforms to train diverse users - spanning high school to post-doc; and what's worked best buff.ly/3jbXJj1
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CancerGenomicsCloud retweeted
As director of @theNCI, I am concerned that delayed and deferred cancer care will increase cancer mortality. The strong, steady progress we have seen the past three decades is at risk.
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CancerGenomicsCloud retweeted
👋 academic twitter, please help me share - opportunity for folks at any university to drive heart, lung, blood, & sleep research. @nih_nhlbi accepting apps for BioData Catalyst Fellows; supporting ambitious research & new tool dev. June 26th deadline biodatacatalyst.nhlbi.nih.go…
CancerGenomicsCloud retweeted
Thanks to funding from @cziscience, looking forward to making new @commonwl learning materials with real-world data from the global Personal Genome Projects and using the Arvados platform. #FOSS #FreeKnowledge #OpenScience
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CancerGenomicsCloud retweeted
Patient derived xenograft models from across PDXNet consortium (@jeffgenome @dennisadean2) reproducibly predict drug responses despite experimental protocol variability. Analysis and data on the @genomicscloud; Open-access article @CR_AACR buff.ly/2KSfAeR
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CancerGenomicsCloud retweeted
Get started with the Common Workflow Language (@commonwl) and #CWL reference implementation cwltool in our latest remote #training session with Stian Soiland-Reyes @soilandreyes & Robin Long. Register now! 📅 29 April 🕜13:00 – 15:30 BST bioexcel.eu/events/reproduci…
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CancerGenomicsCloud retweeted
Five years ago we released our first version of Seurat. Since then, its been extraordinary to watch the growth of this field and to be part of an uplifting, open, and collaborative community developing analytical tools for single cell genomics.
Try out 1st software release from my lab at @nygenome - Seurat: R toolkit for single cell genomics. Code, tutorials- satijalab.org/seurat
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To help design a potential new #CommonWL feature, we are crowd-sourcing examples of non-toy workflows that use dynamic looping: github.com/common-workflow-l… #SciWorkflows
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CancerGenomicsCloud retweeted
Our LDlinkR paper is online today in @FrontGenetics. LDlinkR is a new R package for rapidly calculating linkage disequilibrium statistics in diverse populations. Great work @tim_myers! frontiersin.org/articles/10.… #NCI_ITEB #rstats #LDlink #LDlinkR @NCIEpiTraining