See for example some details on their 2014 pumpkin:
The @phylogenomics lab pumpkin started out simple: @casettron @hhollandmoritz (1/2) pic.twitter.com/gZJNMqPzaf— David Coil (@davidacoil) October 29, 2014
And thus, the @phylogenomics lab annual pumpkin was created. You have to look through the objectives to see it. pic.twitter.com/G3t5Iyo6gL— Russell Neches (@ryneches) October 29, 2014
The pumpkin entry from @phylogenomics's lab is a little unusual! pic.twitter.com/4sNslv9x8x— The Genome Center (@genomecenter) October 30, 2014
From the front of @phylogenomics's lab 'pumpkin' entry pic.twitter.com/Ym55nQ7eba— The Genome Center (@genomecenter) October 30, 2014
From the front of @phylogenomics's lab 'pumpkin' entry pic.twitter.com/Ym55nQ7eba— The Genome Center (@genomecenter) October 30, 2014
And I have on and off carved pumpkins on sciency themes every once in a while.
So this year, when the Genome Center admins sent around an email saying they had bought pumpkins for people to use, I decided it would be fun to do something this year. But then 10/30 came and we had still not done anything.
So I came up with a crazy idea. Cut up pumpkins in different ways as an example of genome sequencing strategies. And, with the help of a few people in my lab and some of the people in neighboring labs, this is what we did.
So - first - we took three pumpkins.
And we decided to make one of them a representation of long read sequencing and another a representative of short read sequencing. So - using a saw provided by people in Justin Siegel's lab, I cut one pumpkin into horizontal slices and remove the innards and made that the "long read sequencing" example. And then I took pumpkin #2 and again cut into horizontal slices but this time I then cut those slices up into chunks. And we then stored the pumpkin pieces overnight and Katie Dahlhausen in my lab made some nice signs to add to the display. In addition, the decorated pumpkin #3 with some "Shotgun sequencing" motifs. And voila, we had our pumpkins ready for the contest for 10/31.
So I headed in to work early, and set up our display.
And I posted about it to Twitter.
Our pumpkin assembly challenge has begun cc: @PhDKD pic.twitter.com/jXyBFv9gBx— Jonathan Eisen (@phylogenomics) October 31, 2018
But something seemed lacking. So I went and got another pumpkin
And before anyone complains I am running the HiC pumpkin reds now but the cross linking is hard to get right pic.twitter.com/AssYCdJPZ1— Jonathan Eisen (@phylogenomics) October 31, 2018
And now it felt complete.
Ok have added the short piece w/ cross linking set to the display pic.twitter.com/Z2ugCb7n7A— Jonathan Eisen (@phylogenomics) October 31, 2018
And then, after the symposium I decided - hey - we should try to reassemble these. I took some pics of this and made them into videos / gifs.
Long piece assembly.
Assembling the long piece pumpkin shotgun was easy.
OK - so - with the help of @casettron @PhDKD @MDeLeon_frogger we were able to use the long pieces and do a whole pumpkin assembly -- pic.twitter.com/LFFOaJ9ziU— Jonathan Eisen (@phylogenomics) October 31, 2018
Linking assembly.
Assembling from the linking pieces was harder. And in the end we did not quite get it back together.
SO - the pumpkin assembly from the short pieces with cross linking was, um, more challenging - but we (me, @casettron @PhDKD @MDeLeon_frogger) got it nearly perfect in the end) pic.twitter.com/XLZEDnzlAE— Jonathan Eisen (@phylogenomics) November 1, 2018
We did not even try to assemble the small pieces. But the next day I did ponder recovering them and the other pieces and doing a meta pumpkin assembly.
So - this morning I checked the CompostBin in the @genomecenter and our pumpkin pieces were still there - am thinking of trying to recover them to a pumpkin piece forensics project - time for some #MetaPumpkin Assemblies pic.twitter.com/0eLJw2Ah8O— Jonathan Eisen (@phylogenomics) November 1, 2018
Anyway - this ended up being pretty fun. Lots of ideas about how to do it better (e.g., we should have barcoded / labelled the pieces so that we could guide the assembly if we failed to do it without guidance). And thanks to all the discussions with people out there and to the people in my lab who helped put this all together.
Also I made a Wakelet of some of the Twitter discussion
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