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Distractions and amusements, with a sandwich and coffee.

Without an after or a when.
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On March 14th celebrate `\pi` Day. Hug `\pi`—find a way to do it.

For those who favour `\tau=2\pi` will have to postpone celebrations until July 26th. That's what you get for thinking that `\pi` is wrong.

If you're not into details, you may opt to party on July 22nd, which is `\pi` approximation day (`\pi` ≈ 22/7). It's 20% more accurate that the official `\pi` day!

Finally, if you believe that `\pi = 3`, you should read why `\pi` is not equal to 3.

2013 was the first year in which I made `\pi` day art. It was a year of dots and love.

René Hansen has created an interactive version of this year's posters! Why not go to the Feynman point directly!

All the posters are also available without the "`\pi` day 3 · 14" inscription.

`\pi_i` / grey 80% opacity

`\pi_i`/`\pi_{i+1}` 80% opacity

`\pi_i` / grey 80% opacity (equal neighbours connected)

`\pi_i` / `\pi_{i+1}` 80% opacity (equal neighbours connected)

— / `\pi_{i+1}` (equal neighbours connected, unconnected digits not shown)

`\pi_i` / `\pi_{i+1}` (equal neighbours connected with line width proportional to difference in neighbour digits `d in \{0,1,2\}`, unconnected digits not shown)

`\pi_i` / `\pi_{i+1}` (equal neighbours connected with line width proportional to difference in neighbour digits `d in \{0...5\}`, unconnected digits not shown)

`\pi` : — / red (equal neighbours connected, unconnected digits not shown)

`\phi` : — / white (equal neighbours connected, unconnected digits not shown)

`e` : — / grey (equal neighbours connected, unconnected digits not shown)

`\pi_i` / grey 80% opacity (equal neighbours connected)

`\pi_i` / `\pi_{i+1}` 80% opacity (equal neighbours connected)

`\pi_i` / grey 80% opacity (equal neighbours connected, unconnected digits not shown)

`\pi_i` / `\pi_{i+1}` 80% opacity (equal neighbours connected, unconnected digits not shown)

Data visualization should be informative and, where possible, tasty.

Stefan Reuscher from Bioscience and Biotechnology Center at Nagoya University celebrates a publication with a Circos cake.

The cake shows an overview of a de-novo assembled genome of a wild rice species *Oryza longistaminata*.

The presence of constraints in experiments, such as sample size restrictions, awkward blocking or disallowed treatment combinations may make using classical designs very difficult or impossible.

Optimal design is a powerful, general purpose alternative for high quality, statistically grounded designs under nonstandard conditions.

We discuss two types of optimal designs (D-optimal and I-optimal) and show how it can be applied to a scenario with sample size and blocking constraints.

Smucker, B., Krzywinski, M. & Altman, N. (2018) Points of significance: Optimal experimental design *Nature Methods* **15**:599–600.

Krzywinski, M., Altman, N. (2014) Points of significance: Two factor designs. Nature Methods 11:1187–1188.

Krzywinski, M. & Altman, N. (2014) Points of significance: Analysis of variance (ANOVA) and blocking. Nature Methods 11:699–700.

Krzywinski, M. & Altman, N. (2014) Points of significance: Designing comparative experiments. Nature Methods 11:597–598.

An illustration of the Tree of Life, showing some of the key branches.

The tree is drawn as a DNA double helix, with bases colored to encode ribosomal RNA genes from various organisms on the tree.

All living things on earth descended from a single organism called LUCA (last universal common ancestor) and inherited LUCA’s genetic code for basic biological functions, such as translating DNA and creating proteins. Constant genetic mutations shuffled and altered this inheritance and added new genetic material—a process that created the diversity of life we see today. The “tree of life” organizes all organisms based on the extent of shuffling and alteration between them. The full tree has millions of branches and every living organism has its own place at one of the leaves in the tree. The simplified tree shown here depicts all three kingdoms of life: bacteria, archaebacteria and eukaryota. For some organisms a grey bar shows when they first appeared in the tree in millions of years (Ma). The double helix winding around the tree encodes highly conserved ribosomal RNA genes from various organisms.

Johnson, H.L. (2018) The Whole Earth Cataloguer, Sactown, Jun/Jul, p. 89

An article about keyboard layouts and the history and persistence of QWERTY.

My Carpalx keyboard optimization software is mentioned along with my World's Most Difficult Layout: TNWMLC. True typing hell.

McDonald, T. (2018) Why we can't give up this odd way of typing, BBC, 25 May 2018.

The theme of the April issue of Molecular Case Studies is precision oncogenomics. We have three papers in the issue based on work done in our Personalized Oncogenomics Program (POG).

The covers of Molecular Case Studies typically show microscopy images, with some shown in a more abstract fashion. There's also the occasional Circos plot.

I've previously taken a more fine-art approach to cover design, such for those of Nature, Genome Research and Trends in Genetics. I've used microscopy images to create a cover for PNAS—the one that made biology look like astrophysics—and thought that this is kind of material I'd start with for the MCS cover.