Inactive due to current Twitter ownership Genetics lab director @illumina unlocking the 💪 of the 🧬
Los Angeles
Joined April 2008
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Anyone cares I'm over on threads.net more (username stromulus28). At least they are pretending to moderate.
Hey @VRDesktop, if someone offered you a free swap, would you turn in a Quest Pro for a Quest 3?
Not seeing many comparisons out there between these two, obviously the leap from Q2 to Q3 is massive and that is being focused on.
I review and finalize genetic test results, and help the world adopt whole genome sequencing from raw data to patient- and provider-friendly reports. @illumina
Sam Strom, PhD FACMG 💪🧬 retweeted
There has been tons of interest how @Illumina's Complete Long Read technology and assay work. Check out this blog post for details. #bioinformatics #longreads #wgs
If you want more from your genome, Illumina Complete Long Reads may be the solution you didn’t know you needed.
With a completely novel process, this breakthrough solution is helping researchers generate more accurate (and confident) genomes than ever: bit.ly/3X4ehhl
Makes 100% sense. I'm surprised it's even that high, considering the cost and how successful Quest 2 has been. Generally VD has worked great for me on Pro.
Yikes! Hopefully they'll squash this bug soon. Thanks as always for your engagement with the user community. Been enjoying Vertigo 2 lately via VD, so much fun. Can't believe I started my gaming life with a NES light gun, now this 😁
I'm having bad network "burping" on my Quest Pro. Not VD specific, also happens on AirLink too (debug only I swear!). It isn't related to when I move my head. Quest 2 on same setup works near perfect. Both on v54. Could this be the same issue?
My two kids are definitely going to get this shot (and be taught why) as soon as they are eligible. So thankful for this life-saving technology!
1 citizen is now happy? C'mon Sid, gotta give us more of a bonus than that! How is the "cure for cancer" equivalent to "gypsum for 30 turns"??
If you or anyone at a lab is interested in setting this up I have a lead on potential funding but no takers yet on the lab side. Everyone is so busy!
I think the best test for families and providers is WGS + methylation array. Unfortunately this is not available to patients. Despite having the tools needed to get a high chance of clear diagnosis fast, no lab even offers this because of the economics. Working on it!
"draw blood... and..." perform WGS on both!
You can check for deletions, point mutations in UBE3A, UPD (iso) as runs of homozygosity, UPD (hetero) as a lack of maternal variants on chr15. IC defects are usually deletions. Methyl MLPA on proband OK too, but won't get mechanism.
I am not deleting my account, but I did delete the app from my phone and I don't intent to post or read any Tweets given the current ownership.
I'll miss interacting with people on here but I'm not willing to participate in an unmoderated platform. Find me on LinkedIn instead.
Sam Strom, PhD FACMG 💪🧬 retweeted
I will present a poster on Oct 26th at 3pm in #ASHG22 on an application of @illumina Complete Long Read to aid ASO design for treatment of rare AD genetic disorders pathogenic de novo mutation. Many thanks to @n_lorem @ryanjtaft @aligenie and the ICLR team! See U at 2866!
I just heard them call your name at the poster printing session 😅
Didn't see you though! – at Los Angeles, CA