@MichaelGallad

Commercial Sales Leader- Canada and Latin America for Illumina. Also, a terrible runner, please wave.

 Vancouver, British Columbia
illumina.com
Joined October 2013
  • Tweets2.3K
  • Following637
  • Followers605
111Media
Michael Gallad retweeted
Mena Farag@_menafarag10 Nov 2023
Capitalize on high-quality, low-cost, ILMN data! Especially with constantly improving DRAGEN analysis: specialized calling (CYP2D6, HLA, SMA, GBA), repeat expansions, SVs, CNVs..it all comes stock with DRAGEN germline ...dont get me started on somatic pipelines!
Ryan Hegarty@RyanHegarty139 Nov 2023
Most large structural variants in cancer genomes can be detected without long reads | Nature Genetics nature.com/articles/s41588-0…

Most large structural variants in cancer genomes can be detected without long reads

Nature Genetics - JaBbA v1 pinpoints the ‘loose ends’ of large (>10-kb) unmapped structural variants in short-read DNA sequencing, suggesting that about 90% of cancer chromosomal...

nature.com
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Michael Gallad retweeted
CGEn@CGEnSeq4 Aug 2023
Led by CGEn Toronto node's Scientific Director Dr. Stephen Scherer, The Centre for Applied Genomics (TCAG) @SickKidsNews has published 'Gene copy number variation and pediatric mental health/neurodevelopment in a general population' in @hmg_journal academic.oup.com/hmg/article…

Gene copy number variation and pediatric mental health/neurodevelopment in a general population

Abstract. We assessed the relationship of gene copy number variation (CNV) in mental health/neurodevelopmental traits and diagnoses, physical health and co

academic.oup.com
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Running both boxes – at Vancouver, British Columbia
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I s add leads thought that level was made up
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@BCCancer_GSC is pleased to announce the acquisition of an @illumina NovaSeq X Plus sequencer via support from the @InnovationCA as part of the @CGEnSeq. 8 Tb of sequence in 24 hours. For access and any sequencing enquiries please contact [email protected]
Illumina NovaSeq X Plus Sequencer

ALT Illumina NovaSeq X Plus Sequencer

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The Silent Genomes project co led by Drs. Arbour, Caron, and Wasserman (@WyWyWa) is a major step to inclusiveness for First Nations in Canada to have access to genomics. Just a start, but incredible work by this team of collaborators! illumina.com/company/news-ce…

Bridging the diagnosis gap for Canada’s Indigenous children

The Silent Genomes Project is building a first-of-its-kind variant library for First Nations, Inuit, and Métis populations

illumina.com
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Michael Gallad retweeted
Rami mehio@mehio_rami11 Jul 2023
Download DRAGEN v4.2 today! best SNV accuracy yet, with new #ML, multigenome graph, 4 new targeted callers, High sensitivity Mosaic variants in segdup detection, major improvement for CNV < 10kb, T2T and more #bioinformatics #genomics #geneticdiseases shorturl.at/bmwX6
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