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Hey folks! Before launching into this week’s visualization, I’m looking for a bit of feedback. Since November, I’ve settled into a new routine with this newsletter and the YouTube channel. Each week this newsletter introduces a visualization at a 30,000 ft view or discusses a specific topic in some depth (example). The following Monday I post a video critiquing the visualization (example). Then on Wednesday (or Tuesday like this past week), I livestream a video where I recreate the visualization and refactor or modify the visualization based on Monday’s critique (example). This is working well for me. I’m honestly surprised that I’m able to find new things each week in Nature and its upper echelon journals without too much effort. How is this flow working for you? Could you reply to this email and let me know? I’m curious what you think of the livestreams. The metrics YouTube gives me for livestreams are not as strong as they were for my recorded and edited videos. But, I honestly don’t have the time to produce the more polished videos. What could I do to make the livestreams more effective and engaging? A question I asked in the community forum was whether people wanted me to only do the refactoring or if it was ok to do both the recreation and refactoring even if it was clear I didn’t like the plot. The feedback I received was 3 to 1 in favor of doing both rather than just the refactoring. What do you think? Here’s my take. I think recreating the plot has value even if I don’t like it. There are two main reasons. As an example, consider the stacked bar plot I discussed last week. First, recreating a visualization forces me to do things that I wouldn’t normally do. For example in last week’s visualization the authors were able to create what were effectively section headings within the legend for taxa that stained Gram-positive or -negative. If I went directly to the line plots without recreating the stacked bar plot, I wouldn’t have had the chance to think about how to recreate that look. I think this blew people’s brains when I did this on the livestream. The second reason is that recreating a visualization tells me a lot about the data and the approach the investigators took to creating the plot. For example, in the stacked bar plot example, it was only by digging into the actual data that I was able to see that there were actually other minor populations not shown in the legend. It also helped me notice they were doing weird things with pooling time points in Figure 5. Even if I never publish a stacked bar plot of my own data I was able to learn a lot by recreating this one. Do you find my logic compelling? Let me know! This leads in nicely to this week’s visualization. I’ll show my cards right away and tell you I’m not a fan of this set of panels from the paper, “Specialized RNA decay fine-tunes monogenic antigen expression in Trypanosoma brucei” published earlier this week in Nature Microbiology. I’ll say more on Monday, but it’s effectively a volcano plot in a polar coordinate system (WHY!?!?). Even if I never use The thing I’m most excited to figure out is the legend. You’ll notice that they have three colored circles under the title of “VEX known interactors” and the two other categories have a single circle. How would we recreate this look? I think it’s actually a lot like the legend in last week’s visualization. As a reminder, here it is: I recreated it by using an aesthetic (e.g., For this week’s legend, imagine if we had taken the same legend we had last week and replaced the The other added wrinkle here is that we effectively have three legends. For the radial volcano plot, I’ll likely use the I’m not sure when I’d want to add this type of structure to my legends. But these types of recreation exercises allow me to do two things. First, they force me to do something that I wouldn’t naturally think of doing. If I jumped directly to the refactoring, this design element wouldn’t be necessary and I’d easily blow off doing it. Second, it forces me to do some problem-solving using the powerful tools I have at my disposal. This reminds me of how I was bothered by the bleed through of a grid line behind a dashed line that I had in a recent visualization. My solution was to put a thick white line down followed by a thin dashed line. I noticed that I still had bleed through of the dashed line from behind my jittered points because I was using
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Hey folks! I just got back from a seminar. I’m still trying to stretch out my eyes from straining to see the small text on each slide! If you don’t know why I’m brining this up, then you must have missed the videos I posted earlier this week. I was discussing the factors we should consider when converting figures designed for papers to figures designed to a slide deck. You can see me critique a figure from my own lab here and the livestream where I refactor the figure can be found here. I’d...
Hey folks, I was a student-invited speaker at the Syracuse University Biology department this week. It was great to meet with them and hear how they are benefiting from these newsletters and my videos. As much as I love posting newsletters and videos, seeing people light up at ideas, laugh at my jokes, and tell me how they are using what I teach them is like jet fuel. I actually gave two talks. One talk covered what I’ve learned about data visualization by critiquing, recreating, and remaking...
Hey folks, If you missed Wednesday’s livestream, I encourage you to go back and check it out. I recreated a panel from a paper published in Nature that is pretty typical. It was made up entirely of photographs. Sometimes I feel like I’m the only PI that doesn’t merge panels into figures using Illustrator or Powerpoint. I prefer to use R with some help from {cowplot} or {patchwork} to do this for me. That way I can write a single script to generate the entire set of panels. The result is a...