Видео

Video cuts off right when it was getting good

RIP roger. May your legacy continue to fluoresce.

Both the removal of scaffolding and the protein insertion machines as well as all the other unnamed irreducible complexity and interdependencies scream out Wonderfully Designed. Yet without any scientific evidence or explanation attributes their existence to the god of the evolutionary gaps, 'it evolved'. Has anyone ever explained a naturalistic process that could actually engineer this - or do we really have to rely on that oft repeated story?

Thank you very much for the tutorial! Can it be used for detecting cells in 3D images?

Isn't there a mistake on 9:27? I think the Fourier image should be rotated on 90 degrees, coz in the direction of x there are many freaquences due to sharp steps.

Very interesting about nothing.

great video. I needed this!

sir i need a little help in selecting probe for my research can u please help me by ur kind suggestion

FACS sorting hehe

Great explanation professor

The very first virus

This was crummy. There are many logical gaps in the presentation. E.g., it is not clear how clusters have the same sequence. There are other RUclips videos on NGS that are clearer.

Great explanation 👌

I found this video very interesting. I have experience with mass spectrometer (LCMS) but this was interesting as it uses a similar principle.

kon kon class 8 me h or kis kis ko ye video goggle se mila h like karo

What a revelation! That Huygens figured out the fundamentals in 1690 is also mind-blowing. Thank you for this fascinating presentation. It utterly changed the way I think about light and optics.

Can someone help me? I read a study that said they "looked at the various forms of the gene coding for a vasopressin receptor" among various people. Does that mean they only looked at active genes, or inactive ones as well?

How can you quantitate your images is vitally important because cellular processes are governed by the laws of physics. To help people with biology we need a physically accurate picture of the cell. Fluorescence excitation causes changes in the eigenstate of the electronic energy levels of the excited molecules, which can result in radiation that changes the state of neighboring molecules. However, fluorescence excitation still remains a powerful tool for measuring the rates of cellular processes. Dr. Dray always concludes her videos with sunscreen and subscribe because all humans are in a race against time to slow down the dynamics of radiation causing protein and DNA mutation in their cells.

Skip to 14:00 if you just care about microscope

I just want to say that you're a great teacher! Passing on not only knowledge but also the passion!

Thanks a lot to give this presentation!

How do i import images on cellprofiler and how can i get a software that works on windows 7

Thanks a lot. What would happen if instead of putting 5% PhiX in the cartridge, I mistakenly put more amount (60%). And I put the correct amount from the library?

amazing lifesaver

Thanks so much! Even the illumina webinar was not as clear as your presentation! 👏👏👏👏

Thank you for the great explaination!

this is great!

Is it safe then to assume that molecules that divide would be the point at which inorganic becomes organic and chemistry becomes biology?

Thanks. Can you clarify at 8:04 when you said each beads has many barcoded oligo-dT oligos on its surface. What is the scale of this "many"? Millions? Are these supposed to attach to the entire transcriptome of a cell?

17:13 quantifying proteins using DNA sequencing (CITE-Seq) 21:26 universal antibodies for a universal cell-surface protein that have unique barcodes for each cell to detect the unwanted doublets (droplet with one bead but two cells)

Awesome

What is the purpose of waving your hands?

Please don't wave your hands--it is very distracting

Amazing overview Excellent

Nice talk!

Very detailed and clear! No ads interrupting! Thank you very much professor!

Thank you! It helped me a lot

I looking for good videos in how analyzing the a dataset of Peripheral Blood Mononuclear Cells (PBMC) ?? Thank you

fourier transfer of fourier himself is such a nerd thing to do lol, love this lecture Thanks!

Great lecture!

Fantastic video! You explain very well

روى ابن ماجه وغيره أن النبي صلى الله عليه وسلم قال: إن مما يلحق المؤمن من عمله وحسناته بعد موته علما علمه ونشره، وولدا صالحا تركه، أو مصحفا ورثه، أو مسجدا بناه، أو بيتا لابن السبيل بناه، أو نهرا أجراه، أو صدقة أخرجها من ماله في صحته وحياته تلحقه بعد موته. m.ruclips.net/video/-qgsOvwlK0w/видео.html&pp=ygUg2KfZhdis2KfYr9mG2Kcg2LnZhdix2Ygg2YXYrNiv2Yk%3D

Thanks for this great presentation!

how does this not have more views

Best lecture

Great stuff, will be featuring you in our next episode!

If you are really interested on, u can dive in Jost 2018 (measuring differentiation). He argue about the limitations of Fst and its relative statistics (yes, there's a lot). You will see that comparing expected heterozygosity as a proxy of differentiation might fail at the populational level in several occasions. For instance, it can only reaches 1 if there are no allelic sharing, and put 11% of differentiation when there are 35% of allelic differences because it rely on the average of a possible heterozygosity that might comes from a loci in case of panmixing breeding (a lot of assumptions). Jost argue that it would be more helpful try to compare the frequency of alleles, mainly for those loci (or markers) that can measure a multialellic state ( more than two, usually). Fst still usefull, but you can't take that as the ultimate tool to measure everything. Remember, a 30 inch ruler is useless to measure the distance between the sun and the earth or the circumference of a cell.

Great video and great information

Great to hear

talking bullshit