Mike Marsh

@TMSSociety, I want to learn more about MDiscovery and check out the data, but the webpage doesn't have any way to contact or get more info. What do you recommend? tms.org/SpecialtyCongr…

@IneRoss What would you want to change them to? You could use the intensity calibration tool to apply a different intensity scale if you know exactly what numbers you want to display. You can hide the legend altogether, but I don't think you can hide the numbers but show the colorbar.

@DragonflyWizard Help! Is it possible to change the numbers displayed on the intensity scale bar? Alternatively, removing the numbers and ticks? Thank you!

@jaimiAgray You should reach out, maybe we could have an informal webinar for the UTCT team to visit pain points and share best practice tips!

@danpaluh @jaimiAgray Probably yes to VGL/RAW image files. Maybe not on other saved VG results, but we could discuss further.

@jaimiAgray Nice! Sometimes when you get a good tool going, it's hard to consider switching to something else. I felt like it was hard to get you and your Florida Museum team to consider moving to Dragonfly. I suppose your new colleagues at Texas gave you a gentle nudge. And you like it!

@benjaminbarad Hi Ben, glad everything went well! Can you update your Dragonfly links to point to dragonfly.comet.tech ?

One of the coolest thing about this class is that the tutorials are almost all online already! Mine is at baradlab.com/michigan_tutor…. I caught a bunch of issues during the practical that I will clean up in the next few days, but hopefully this is a useful resource for some folks.

@parameciumbrain @MicroscopyToday @NicolasPiche Benjamin Provencher, Eric Yen, and @BetterVizBill . But I couldn't make it this year.

@MicroscopyToday Not sure who all is there this year!

You should also go harass whoever is at the Dragonfly booth (425) if you're at #MM2023. I do ALL of my segmentations and deep learning in Dragonfly and you should too! Go grab a license or a trial from them and make pretty segmentations too!

RT @AntonDragonfly: New logo, new brand, same Dragonfly software. There has never been a better time to get your perpetual Dragonfly licens…

@CygnusPlantXray I always had you pegged as the sort of hoopy frood who knows where his towel is.

@vinfernand I have 2-3 extra in my bag. Hope that is enough for whoever forgets.

Day 1 in the books. Breathing a little easier now. It helps when your user base is such a great community. Go Dragonfly Nation!

I don't recommend event planning as a side gig. The stress of planning your first conference (hybrid meeting) without neglecting your normal full time responsibilities. 😬

@HollyRHendo I believe Rigaku will post it pretty quickly...1-2 days.

@DragonflyWizard Hi Mike, any chance this will go up on YouTube after? As annoyingly will be on my daughter’s bathtime here in the UK!

So... Subject labelled me an expert... Register now so you can watch live.

Er... That should read "Someone labelled me an expert." Now we can be certain I am not an expert in posting to social media.

@saroberts @OrsDragonfly3D It's not as bad as you think. You can turn off data augmentation and see the CUDA usage exceed 90%. But I think your training will converge sooner if you maintain augmentation. Don't let it bother you that the CPU is doing its share.

Hey @OrsDragonfly3D users! What do you do to best utilize your GPU when training DL segmentation models! Some (Sensor3D) seem to work efficiently on their own, making the GPU burn! Others (U-Net) don't max out CUDA. Any tips?

@SwuliusLab @parameciumbrain Good luck getting home ahead of the storm! Safe travels.

@parameciumbrain I'm in.

So... our flight got delayed and we have 12 hours to kill. Anyone want to do dinner tonight? #BPS2023

If you're at Biophysics, by sure to check out Jess's poster today!

@Geo_XCT It seems to be standard everywhere except TEM. They have been looking at everything with inverted contrast for decades.

@Geo_XCT I definitely have a preference! White on black (where white is the abundance of signal and black is the absence of signal). That is what i call "positive contrast" and, it is the easiest to interpret in a way that is consistent with histogram and other image analysis tools.

The guessing game is back! just this time is way too easy so no guessing 🤣🤣but it will resume shortly (aka when I actually have the time!) but I had finally some time to put through the X-rays this beautiful shell found on the beach by our very own technician

@kisharrington Sorry. I shouldn't call these abstracts. These are short proceedings papers.

@kisharrington Wow! If you hadn't posted this, I would miss this oppty to present in exactly the perfect forum. Thanks Kyle! Look for my rushed--but otherwise perfect :) --abstract soon!