Just in case you weren’t aware, ASAPbio is currently underway and is likely going to influence the future of science publication!!
Accelerating Science and Publication in Biology (ASAPbio) will be an interactive meeting to discuss the use of preprints in biology held on February 16-17, 2016. The meeting will be streamed online, and we welcome participation from all interested parties through this website and on Twitter (#ASAPbio).
For background on the issues facing science publication, especially in biomedical science and biology, check out this primer from Nature last week (Does it take too long to publish research?). We here at CauseScience think that the answer to that title is a resounding YES!! One option that ASAPbio is considering are preprints – commonly used in other science fields. Nature this week featured another article related to ASAPbio about preprints (Biologists urged to hug a preprint).
For up to date info on the conference, check out the twitter hashtag #ASAPbio, which thus far has included tweets from well-known scientists, and fun pictures of former NIH directors and Nobel Laureates!! Or just visit the ASAPbio website!!
Definitely exciting to see people discussing the problems of science publication, but more importantly, discussing potential solutions!!
crestwind24- I am spending part of my day processing images (micrographs) that I took earlier on our labs confocal microscope. As I mentioned in a previous CauseScience Friday, the confocal allows me to take amazing pictures of neurons and their axons and dendrites. Today I am taking many images taken through the depth of a worm and making 3D animations. This allows you to see the morphology of the axons – or where they are in space. Below is a partial low-res GIF I made of one of my animations – it shows two neurons and their axons in C. elegans!!
psgurel- Part of joining a new lab involves developing a new project. Today, I’m doing some test runs as an initial step in developing a method for imaging different conformations of actin filaments for cryo Eelectron Microscopy. First, I have to coat EM grids in a mechanism that will allow the actin to bind properly, so I’m surveying different ways of coating EM grids. Wish me luck!