BaseSpace Suite
@BaseSpace
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Illumina BaseSpace Suite: integrated informatics to power precision medicine. Learn about our recent developments: https://t.co/q7ZZSoFCu7 #DRAGEN #BaseSpace
San Diego
Joined November 2012
Considering running @10xGenomics Visium libraries on your @illumina sequencer? Check our fourth post from the series about publicly available sequencing data on BaseSpace to see what to expect:
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Interested in running @10xGenomics Multiome libraries on your @Illumina sequencer? Check our third post from the series about publicly available sequencing data on BaseSpace to see what to expect:
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See our new post on the blog to learn about the Demo Data section of BaseSpace Sequence Hub, where we post typical run data from the latest sequencers and prep products from @illumina and others:
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Customers often ask how to tell if their sequencing run looks good. See our new post on the blog for things to check for: Does my sequencing run look good?
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We're proud to share the updated @Illumina Research and Innovation website for the latest in cutting-edge genomics research from the scientists that help drive progress in how we aggregate, analyze, and interpret genomic data for meaningful insights.
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#DRAGEN pipelines deliver highly accurate variant identification, and are available on BaseSpace Sequence Hub for easy access. Learn more at
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Take advantage of our #DRAGEN accelerated COVID analysis pipeline to call variants with accompanying Lineage tools, available as easy to deploy docker containers onsite or in the cloud.
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One of the big challenges to doing COVID variant surveillance is interpretation of SARS-CoV-2 sequencing data. Kudos to the @illumina DRAGEN team for releasing these free @basespace Apps to analyze and share data. https://t.co/3Zwvf5NrM2
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Committed to reducing the genomic data deluge, DRAGEN v3.8 can compress the human #genomic data footprint by up to 5x. The realization of our Enancio acquisition, v3.8 offers lossless compression reducing storage costs by up to 80%. https://t.co/NsxyAHT8be
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Great paper in @NEJM showing the superiority of WGS over traditional cytogenetics for Myeloid Cancers. NovaSeq data analysed with #DRAGEN and @BaseSpace demonstrating the speed & accuracy of the full @illumina workflow https://t.co/Ww4KXO5tBB
nejm.org
Genomic analysis is essential for risk stratification in patients with acute myeloid leukemia (AML) or myelodysplastic syndromes (MDS). Whole-genome sequencing is a potential replacement for conven...
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#DRAGEN v3.8 enables cost-savings with ORA Compression technology, extended biomarker capabilities, and more! Learn more in our upcoming webinar.
Join us to learn what the #DRAGEN team has been busy with the last few months. @HeidiHnorton
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Excited to announce that customers using @nanostringtech #GeoMx with @illumina NGS can now use @basespace to streamline and accelerate analysis using #DRAGEN technology. Read more here on our blog post:Â https://t.co/cOnGjiKeF7 Â #spatial
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A catalyst for scientific discovery, ICA allows our customers to quickly analyze new samples & leverage under-utilized #genomic data with a sophisticated data science environment. Illumina Connected Analytics is commercially available now. https://t.co/X5gDikwNMd
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We’re excited to share about our #collaboration with @nanostringtech to bring #GeoMx digital #spatial profiling to @illumina NGS and @basespace users! We're in early access now, and will roll out rapid developments throughout 2021. More on the blog:
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All the main #DRAGEN pipelines and DRAGEN Enancio compression are now available on Illumina's Connected Analytics platform #ICA. https://t.co/NbnjoVB5TF
@susantousi @HansCobben @HeidiHnorton @jaylpatel
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DRAGEN v3.7 is now available!
The Illumina informatics team is excited to announce DRAGEN v3.7 with winning PrecFDA Germline pipeline, major somatic variant calling improvements, super fast #singlecellRNA pipeline, full UMI support, & a targeted CYP2D6 caller! https://t.co/VFKDgWCXAF
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ICYMI: @illumina's #DRAGEN Bio-IT platform provides accurate secondary analysis of #NGS data. Partnering w/@AWScloud, we’re honored to serve the scientific community by making the comprehensive reanalysis of the 1kGP freely available. Great work, team. https://t.co/dHmhYpgdEI
aws.amazon.com
Guest authored by Bryan Lajoie, Staff Bioinformatics Scientist at Illumina Inc. — We are pleased to announce the release of a comprehensive reanalysis of 3,202 deeply-sequenced samples from the 1000...
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Illumina's ExpansionHunter Software Shows Clinical Promise for STR Expansions
genomeweb.com
The firm's CLIA lab presented data at the virtual ASHG meeting showing how it validated WGS-based STR expansion analysis to diagnose rare disease.
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DRAGEN v3.7 is out, another monster release that introduces our first version of accelerated Single Cell RNA pipeline, integration of CYP2D6 caller, extension of UMI based pipelines, major accuracy improvements for T-only samples and more. #DRAGEN
https://t.co/wAROEJeMSM
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Missed today's @GenomeWeb #DRAGEN-GATK webinar featuring Eric Banks @gatk_dev & Severine Catreux @illumina? Here's a great writeup from @VdaGeraldine
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