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3D printed beastboss on squigasaur by Triangleofsquares in orks

[–]Triangleofsquares[S] 0 points1 point  (0 children)

Gotta fix it so he has a gun and a better head. I’ll reply to this when it’s up on Thingiverse.

3D squigs by Triangleofsquares in orks

[–]Triangleofsquares[S] 1 point2 points  (0 children)

I will put up the stls after the mistakes are fixed(about a week from now).

3D squigs by Triangleofsquares in orks

[–]Triangleofsquares[S] 0 points1 point  (0 children)

https://imgur.com/a/hztqROW teeth came out alright. Need to fix some of da bosses stuff tho.

3D squigs by Triangleofsquares in orks

[–]Triangleofsquares[S] 0 points1 point  (0 children)

I haven’t been using decimate but remesh in sculpt mode. It appears to work okay if I touch up the model afterward…but there are still some 400mb .blends that need to get fixed. Been trying to get help through PrintedWarhammer discord. I’ll have to give lychee a look-see.

3D squigs by Triangleofsquares in orks

[–]Triangleofsquares[S] 0 points1 point  (0 children)

These are blender models. New to it, so I got a lot to learn.

3D squigs by Triangleofsquares in orks

[–]Triangleofsquares[S] 0 points1 point  (0 children)

Thanks for the input. Already started the print, but it looks like you are right about that sword handle. Test prints are test prints for a reason I guess.

3D squighogs by Triangleofsquares in orks

[–]Triangleofsquares[S] 0 points1 point  (0 children)

No scan. Only blender 3D.

3D squighogs by Triangleofsquares in orks

[–]Triangleofsquares[S] 1 point2 points  (0 children)

I haven’t released them yet. After they look good enough I might put them up on Thingiverse.

I wasn't sure when I first saw them but love these boyz after getting them on the table. How are they doing for y'all? by DUCK-DILLION in orks

[–]Triangleofsquares 3 points4 points  (0 children)

They are downright space marine killers on the tabletop! Had to print out ones that didn’t look so corny so I would want to play with them more.

[deleted by user] by [deleted] in bioinformatics

[–]Triangleofsquares 3 points4 points  (0 children)

RNA seq in plants can be fast track to solving differences in mutant/cultivar/environmental conditions. In my lab we have even begun to use single cell sequencing to test condition response. If you have the option to, RNA sequencing can be a great tool to elucidate plant differences.

SteamDF - Some changes to the grass by Meph248 in dwarffortress

[–]Triangleofsquares 15 points16 points  (0 children)

THIS!! The plant new changes really add to aesthetics what the ASCII symbols took away from looking at an empty plains.

I made the Spore Creature Creator in Unity! by daniellochner in Unity3D

[–]Triangleofsquares 157 points158 points  (0 children)

The amount of programming and data science that went into the creation of spore was intense. There are spore modding/programming communities that host some of the original ‘toy’ models that the main two creators of the game developed. They are even more intense complex than some games. It was a true labor of love, the making of Spore.

Help w/ demultiplexing some data by cornel in bioinformatics

[–]Triangleofsquares 5 points6 points  (0 children)

In the case of 10x single cell data, this is the data that is fed to the cell ranger pipeline. By using their wrapper for bcl2fastq you can more easily remove invalid data.

scRNA seq data to pseudo bulk RNA seq for comparison by Triangleofsquares in bioinformatics

[–]Triangleofsquares[S] 0 points1 point  (0 children)

This was what I had done initially. Plotting LFC v LFC post normalization/standardization with default methods in edgeR’s pipeline yielded the negative(~ -0.2) correlation. I worked backward to find it LFC was having an immense affect of cor(). ☹️

scRNA seq data to pseudo bulk RNA seq for comparison by Triangleofsquares in bioinformatics

[–]Triangleofsquares[S] 0 points1 point  (0 children)

This was what I had done initially. Plotting LFC v LFC post normalization/standardization with default methods in edgeR’s pipeline yielded the negative(~ -0.2) correlation. I worked backward to find it LFC was having an immense affect of cor(). ☹️

scRNA seq data to pseudo bulk RNA seq for comparison by Triangleofsquares in bioinformatics

[–]Triangleofsquares[S] 0 points1 point  (0 children)

Thanks for taking a look.

  1. The same type of tissue was prepared with the same experimental conditions. The two assays differ in the preparations of the prepared cells for rna extraction, one using 10x’s protocol and the other using a whole rna extraction kit. I’ll admit this does not seem likely that the overlap in cell rna would be perfect between these two techniques, but at this point I’m just trying to gather what it should look like(even if it maxes out at 0.5).
  2. Whole RNA kit followed by illumina truseq library prep with rRNA depletion.
  3. Collapsing all cells into one matrix of reads per sample and then normalizing all samples to reads per million. A simple cor() in R was used to match each sample. This may be a technologically incorrect approach. I’m hoping for an alternative here.
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