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Country flags are pretty colorful and some are even pretty.

Instead of drawing the flag in a traditional way (yawn...), I wanted to draw it purely based on the color proportions in the flag (yay!). There are lots of ways to do this, such as stacked bars, but I decided to go with concentric circles. A few examples are shown below.

Once flags are drawn this way, they can be grouped by similarity in the color proportions.

Check out the posters or read about the method below.

Or, download my country flag color catalog to run your own analysis.

To determine the proportions of colors in each flag, I started with the collection of all country flags in SVG from Wikipedia. The flags are conveniently named using the countries' ISO 3166-2 code. At the time of this project (21 Mar 2017), this repository contained 312 flags, of which I used 256.

I originally wanted to use the flag-icon-css collection, but ran into problems with it. It had flags in only either 1 × 1 or 4 × 3 aspect ratio, which distorted and clipped many flags. Many flags were also inaccurately drawn and had inconsistent use of colors. For example, in Turkey's flag the red inside the white crescent was slightly different than elsewhere in the flag.

I converted the SVG files to high resolution PNG (2,560 pixels in width) and sampled the colors in each flag, keeping only those colors that occupied at least 0.01% of the flag. I apply this cutoff to avoid blends between colors due to anti-aliasing applied in the conversion. When drawing the flags as circles, I only use colors that occupy at least 1% of the flag—this impacts flags that have detailed emblems, such as Belize. I apply some rounding off of the proportions and colors with the same proportion are ordered so that lighter colors (by Lab luminance) are in the center of the circle.

There are various ways to represent the proportions of the flag colors as concentric rings—in other words, to use symbols of different size to encode area.

The accurate way is to have the area of the ring be proportional to the area of the color on the map. The inaccurate way is to encode the area by the the width of the ring. These two cases are the `k=0.5` and `k=1` columns in the figure below, where `k` is the power in `r = a^k` by which the radius of the ring, `r`, is scaled relative to the area, `a`. A perceptual mapping using `k=0.57` has been suggested by some.

My goal here is not to encode the proportions so that they can be read off quantitatively. To find a value of `k`, I drew some flags and looked at their concentric ring representation. For example, with `k=0.57` the Nigerian flag's white center is too large for my eye while for `k=1` it is definitely too small. I liked the proportions for `k=1/\sqrt{2}` but wasn't happy with the fact that flags like France's, which have colors in equal areas, didn't have equal width rings.

In the end I decided on a hybrid approach in which the out radius of color `i` whose area is `a_i` is `r_i = a_i^k + \sum_{j=0}^{i-1} a_j^k` where the colors are sorted so that `a_{i-1} \le a_i`. If I use `k=0.25`, I manage to have flags like France have equal width rings but flags like Nigeria in which the proportions are not equal are closer to the encoding with `k=1/\sqrt{2}`. In this hybrid approach smaller areas, such as the white in the map of Turkey, are exaggerated. Notice that here `k` plays a slightly different role—it's used as the power for each color individually, `\sum a^k`, rather than their sum, `\left({\sum a}\right)^k`.

For the purists this choice of encoding might appear as the crime of the worst sort, representing neither correct (`k=0.5`) nor the conventionally incorrect encoding associated with `k=1`. Think of it this way—I know what rule I'm breaking.

The similarity between two flags is calculated by forming an intersection between the radii positions of the concentric rings of the flags.

For each intersection, the similarity of colors is determined using `\Delta E`, which is the Euclidian distance of the colors in LCH space. I placed less emphasis on luminance and chroma in the similarity calculation by fist transforming the coordinates to `(\sqrt L,\sqrt C, H)`) before calculating color differences. The similarity score is $$ S = \sum \frac{\Delta r}{\sqrt{\Delta E}} $$

Color pairs with `\Delta E < \Delta E_{min} = 5` are considered the same and have an effective `\Delta E = 1`.

I explored different cutoffs and combinations of transforming the color coordinates. This process was informed based on how the order of the flags looked to me.

I decided to start the order with Tonga, since it had the highest average similarity score to all other flags in some of my trials. The flag that is most different from other flags, as measured by the average similarity score, is Israel.

I couldn't find a list of colors in the flags of countries, so I provide my analysis here. Every country's SVG flag was converted into a 2,560 × 1,920 PNG file (4,915,200 pixels). Colors that occupied at least 0.01% of the pixels are listed in their HEX format, followed by the number of pixels they occupy. The fraction of the flag covered by sampled colors is also shown.

DOWNLOAD #code img_pixels sampled_pixels fraction_sampled_pixels hex:pixels,hex:pixels,... ... cm 4366506 4364514 0.999544 FCD116:1513103,007A5E:1456071,CE1126:1395340 cn 4369920 4364756 0.998818 DE2910:4260992,FFDE00:103764 co 4364800 4364800 1.000000 FCD116:2183680,003893:1090560,CE1126:1090560 ...

DOWNLOAD #code1 code2 similarity_score ad ae 0.0108360578506763 ad af 0.0288161214840692 ad ag 0.0510922121861494 ad ai 0.42746294322472 ... zw ye 0.473278765746989 zw yt 0.238101673130705 zw za 0.810589244643825 zw zm 0.573265751850587

Decision trees classify data by splitting it along the predictor axes into partitions with homogeneous values of the dependent variable. Unlike logistic or linear regression, CART does not develop a prediction equation. Instead, data are predicted by a series of binary decisions based on the boundaries of the splits. Decision trees are very effective and the resulting rules are readily interpreted.

Trees can be built using different metrics that measure how well the splits divide up the data classes: Gini index, entropy or misclassification error.

When the predictor variable is quantitative and not categorical, regression trees are used. Here, the data are still split but now the predictor variable is estimated by the average within the split boundaries. Tree growth can be controlled using the complexity parameter, a measure of the relative improvement of each new split.

Individual trees can be very sensitive to minor changes in the data and even better prediction can be achieved by exploiting this variability. Using ensemble methods, we can grow multiple trees from the same data.

Krzywinski, M. & Altman, N. (2017) Points of Significance: Classification and regression trees. *Nature Methods* **14**:757–758.

Lever, J., Krzywinski, M. & Altman, N. (2016) Points of Significance: Logistic regression. *Nature Methods* **13**:541-542.

Altman, N. & Krzywinski, M. (2015) Points of Significance: Multiple Linear Regression *Nature Methods* **12**:1103-1104.

Lever, J., Krzywinski, M. & Altman, N. (2016) Points of Significance: Classifier evaluation. *Nature Methods* **13**:603-604.

Lever, J., Krzywinski, M. & Altman, N. (2016) Points of Significance: Model Selection and Overfitting. *Nature Methods* **13**:703-704.

Lever, J., Krzywinski, M. & Altman, N. (2016) Points of Significance: Regularization. *Nature Methods* **13**:803-804.

The artwork was created in collaboration with my colleagues at the Genome Sciences Center to celebrate the 5 year anniversary of the Personalized Oncogenomics Program (POG).

The Personal Oncogenomics Program (POG) is a collaborative research study including many BC Cancer Agency oncologists, pathologists and other clinicians along with Canada's Michael Smith Genome Sciences Centre with support from BC Cancer Foundation.

The aim of the program is to sequence, analyze and compare the genome of each patient's cancer—the entire DNA and RNA inside tumor cells— in order to understand what is enabling it to identify less toxic and more effective treatment options.

Principal component analysis (PCA) simplifies the complexity in high-dimensional data by reducing its number of dimensions.

To retain trend and patterns in the reduced representation, PCA finds linear combinations of canonical dimensions that maximize the variance of the projection of the data.

PCA is helpful in visualizing high-dimensional data and scatter plots based on 2-dimensional PCA can reveal clusters.

Altman, N. & Krzywinski, M. (2017) Points of Significance: Principal component analysis. *Nature Methods* **14**:641–642.

Altman, N. & Krzywinski, M. (2017) Points of Significance: Clustering. *Nature Methods* **14**:545–546.

Similar to the `h` index in publishing, the `k` index is a measure of fitness performance.

To achieve a `k` index for a movement you must perform `k` unbroken reps at `k`% 1RM.

The expected value for the `k` index is probably somewhere in the range of `k = 26` to `k=35`, with higher values progressively more difficult to achieve.

In my `k` index introduction article I provide detailed explanation, rep scheme table and WOD example.

I've applied the char-rnn recurrent neural network to generate new words, names of drugs and countries.

The effect is intriguing and facetious—yes, those are real words.

But these are not: *necronology*, *abobionalism*, *gabdologist*, and *nonerify*.

These places only exist in the mind: *Conchar and Pobacia*, *Hzuuland*, *New Kain*, *Rabibus and Megee Islands*, *Sentip and Sitina*, *Sinistan* and Urzenia.

And these are the imaginary afflictions of the imagination: *ictophobia*, *myconomascophobia*, and *talmatomania*.

And these, of the body: *ophalosis*, *icabulosis*, *mediatopathy* and *bellotalgia*.

Want to name your baby? Or someone else's baby? Try *Ginavietta Xilly Anganelel* or *Ferandulde Hommanloco Kictortick*.

When taking new therapeutics, never mix *salivac* and *labromine*. And don't forget that *abadarone* is best taken on an empty stomach.

And nothing increases the chance of getting that grant funded than proposing the study of a new –ome! We really need someone to looking into the *femome* and *manome*.

An exploration of things that are missing in the human genome. The nullomers.

Julia Herold, Stefan Kurtz and Robert Giegerich. Efficient computation of absent words in genomic sequences. *BMC Bioinformatics* (2008) **9**:167