Designing for Color blindness
Color choices and transformations for deuteranopia and other afflictions
Here, I help you understand color blindness and describe a process by which you can make good color choices when designing for accessibility.
The opposite of color blindness is seeing all the colors and I can help you find 1,000 (or more) maximally distinct colors.
You can also delve into the mathematics behind the color blindness simulations and learn about copunctal points (the invisible color!) and lines of confusion.
Color blindness R code
R code for converting an RGB color for color blindness. For details see the math tab and the resources section for background reading.
--- title: 'RGB color correction for color blindess: protanopia, deuteranopia, tritanopia' author: 'Martin Krzywinski' web: http://mkweb.bcgsc.ca/colorblind --- ```{r} gamma = 2.4 ############################################### # Linear RGB to XYZ # https://en.wikipedia.org/wiki/SRGB XYZ = matrix(c(0.4124564, 0.3575761, 0.1804375, 0.2126729, 0.7151522, 0.0721750, 0.0193339, 0.1191920, 0.9503041), byrow=TRUE,nrow=3) SA = matrix(c(0.2126,0.7152,0.0722, 0.2126,0.7152,0.0722, 0.2126,0.7152,0.0722),byrow=TRUE,nrow=3) ############################################### # XYZ to LMS, normalized to D65 # https://en.wikipedia.org/wiki/LMS_color_space # Hunt, Normalized to D65 LMSD65 = matrix(c( 0.4002, 0.7076, -0.0808, -0.2263, 1.1653, 0.0457, 0 , 0 , 0.9182), byrow=TRUE,nrow=3) # Hunt, equal-energy illuminants LMSEQ = matrix(c( 0.38971, 0.68898,-0.07868, -0.22981, 1.18340, 0.04641, 0 , 0 , 1 ), byrow=TRUE,nrow=3) # CIECAM97 SMSCAM97 = matrix(c( 0.8951, 0.2664, -0.1614, -0.7502, 1.7135, 0.0367, 0.0389, -0.0685, 1.0296), byrow=TRUE,nrow=3) # CIECAM02 LMSCAM02 = matrix(c( 0.7328, 0.4296, -0.1624, -0.7036, 1.6975, 0.0061, 0.0030, 0.0136, 0.9834), byrow=TRUE,nrow=3) ############################################### # Determine the color blindness correction in LMS space # under the condition that the correction does not # alter the appearance of white as well as # blue (for protanopia/deuteranopia) or red (for tritanopia). # For achromatopsia, greyscale conversion is applied # to the linear RGB values. getcorrection = function(LMS,type="p",g=gamma) { red = matrix(c(255,0,0),nrow=3) blue = matrix(c(0,0,255),nrow=3) white = matrix(c(255,255,255),nrow=3) LMSr = LMS %*% XYZ %*% apply(red,1:2,linearize,g) LMSb = LMS %*% XYZ %*% apply(blue,1:2,linearize,g) LMSw = LMS %*% XYZ %*% apply(white,1:2,linearize,g) if(type == "p") { x = matrix(c(LMSb[2,1],LMSb[3,1], LMSw[2,1],LMSw[3,1]),byrow=T,nrow=2) y = matrix(c(LMSb[1,1],LMSw[1,1]),nrow=2) ab = solve(x) %*% y C = matrix(c(0,ab[1,1],ab[2,1],0,1,0,0,0,1),byrow=T,nrow=3) } else if (type == "d") { x = matrix(c(LMSb[1,1],LMSb[3,1], LMSw[1,1],LMSw[3,1]),byrow=T,nrow=2) y = matrix(c(LMSb[2,1],LMSw[2,1]),nrow=2) ab = solve(x) %*% y C = matrix(c(1,0,0,ab[1,1],0,ab[2,1],0,0,1),byrow=T,nrow=3) } else if (type == "t") { x = matrix(c(LMSr[1,1],LMSr[2,1], LMSw[1,1],LMSw[2,1]),byrow=T,nrow=2) y = matrix(c(LMSr[3,1],LMSw[3,1]),nrow=2) ab = solve(x) %*% y C = matrix(c(1,0,0,0,1,0,ab[1,1],ab[2,1],0),byrow=T,nrow=3) } else if (type == "a" | type == "g") { C = matrix(c(0.2126,0.7152,0.0722, 0.2126,0.7152,0.0722, 0.2126,0.7152,0.0722),byrow=TRUE,nrow=3) } return(C) } # rgb is a column vector convertcolor = function(rgb,LMS=LMSD65,type="d",g=gamma) { C = getcorrection(LMS,type) if(type == "a" | type == "g") { T = SA } else { M = LMS %*% XYZ Minv = solve(M) T = Minv %*% C %*% M } print(T) rgb_converted = T %*% apply(rgb,1:2,linearize,g) return(apply(rgb_converted,1:2,delinearize,g)) } # This function implements the method by Vienot, Brettel, Mollon 1999. # The approach is the same, just the values are different. # http://vision.psychol.cam.ac.uk/jdmollon/papers/colourmaps.pdf convertcolor2 = function(rgb,type="d",g=2.2) { xyz = matrix(c(40.9568, 35.5041, 17.9167, 21.3389, 70.6743, 7.98680, 1.86297, 11.4620, 91.2367),byrow=T,nrow=3) lms = matrix(c(0.15514, 0.54312, -0.03286, -0.15514, 0.45684,0.03286, 0,0,0.01608),byrow=T,nrow=3) rgb = (rgb/255)**g if(type=="p") { S = matrix(c(0,2.02344,-2.52581,0,1,0,0,0,1),byrow=T,nrow=3) rgb = 0.992052*rgb+0.003974 } else if(type=="d") { S = matrix(c(1,0,0,0.494207,0,1.24827,0,0,1),byrow=T,nrow=3) rgb = 0.957237*rgb+0.0213814 } else { stop("Only type p,d defined for this function.") } M = lms %*% xyz T = solve(M) %*% S %*% M print(T) rgb = T %*% rgb rgb = 255*rgb**(1/g) return(rgb) } ############################################### # RGB to Lab rgb2lab = function(rgb,g=gamma) { rgb = apply(rgb,1:2,linearize,g) xyz = XYZ %*% rgb delta = 6/29 xyz = xyz / (c(95.0489,100,108.8840)/100) f = function(t) { if(t > delta**3) { return(t**(1/3)) } else { return (t/(3*delta**2) + 4/29) } } L = 116*f(xyz[2]) - 16 a = 500*(f(xyz[1]) - f(xyz[2])) b = 200*(f(xyz[2]) - f(xyz[3])) return(matrix(c(L,a,b),nrow=3)) } # CIE76 (https://en.wikipedia.org/wiki/Color_difference) deltaE = function(rgb1,rgb2) { lab1 = rgb2lab(rgb1) lab2 = rgb2lab(rgb2) return(sqrt(sum((lab1-lab2)**2))) } clip = function(v) { return(max(min(v,1),0)) } ############################################### # RGB to/from linear RGB #https://en.wikipedia.org/wiki/SRGB linearize = function(v,g=gamma) { if(v <= 0.04045) { return(v/255/12.92) } else { return(((v/255 + 0.055)/1.055)**g) } } delinearize = function(v,g=gamma) { if(v <= 0.003130805) { return(255*12.92*clip(v)) } else { return(255*clip(1.055*(clip(v)**(1/g))-0.055)) } } pretty = function(x) { noquote(formatC(x,digits=10,format="f",width=9)) } # a dark red rgb1 = matrix(c(0,209,253),nrow=3) # dark green rgb2 = matrix(c(60,135,0),nrow=3) # simulate deuteranopia convertcolor(rgb1,type="d") convertcolor(rgb2,type="d") # get color distance before and after simulation deltaE(rgb1,rgb2) deltaE(convertcolor(rgb1,type="d"),convertcolor(rgb2,type="d")) # transformation matrices for each color blindness type M = LMSD65 %*% XYZ pretty(solve(M) %*% getcorrection(LMSD65,"p") %*% M) pretty(solve(M) %*% getcorrection(LMSD65,"d") %*% M) pretty(solve(M) %*% getcorrection(LMSD65,"t") %*% M) pretty(SA) # method by Vienot, Brettel, Mollon, 1999 convertcolor2(rgb1,type="d",g=2.2) convertcolor2(rgb2,type="d",g=2.2) ```
# a dark red rgb1 = matrix(c(225,0,30),nrow=3) # dark green rgb2 = matrix(c(60,135,0),nrow=3) # simulate deuteranopia convertcolor(rgb1,type="d") [,1] [1,] 136.7002 [2,] 136.7002 [3,] 0.0000 convertcolor(rgb2,type="d") [,1] [1,] 116.76071 [2,] 116.76071 [3,] 16.73263 # get color distance before and after simulation deltaE(rgb1,rgb2) [1] 116.9496 deltaE(convertcolor(rgb1,type="d"),convertcolor(rgb2,type="d")) [1] 12.72204 # transformation matrices for each color blindness type M = LMSD65 %*% XYZ pretty(solve(M) %*% getcorrection(LMSD65,"p") %*% M) [,1] [,2] [,3] [1,] 0.1705569911 0.8294430089 0.0000000000 [2,] 0.1705569911 0.8294430089 -0.0000000000 [3,] -0.0045171442 0.0045171442 1.0000000000 pretty(solve(M) %*% getcorrection(LMSD65,"d") %*% M) [,1] [,2] [,3] [1,] 0.3306600735 0.6693399265 -0.0000000000 [2,] 0.3306600735 0.6693399265 0.0000000000 [3,] -0.0278553826 0.0278553826 1.0000000000 pretty(solve(M) %*% getcorrection(LMSD65,"t") %*% M) [,1] [,2] [,3] [1,] 1.0000000000 0.1273988634 -0.1273988634 [2,] -0.0000000000 0.8739092990 0.1260907010 [3,] 0.0000000000 0.8739092990 0.1260907010 pretty(SA) [,1] [,2] [,3] [1,] 0.2126000000 0.7152000000 0.0722000000 [2,] 0.2126000000 0.7152000000 0.0722000000 [3,] 0.2126000000 0.7152000000 0.0722000000 # method by Vienot, Brettel, Mollon, 1999 convertcolor2(rgb1,type="d",g=2.2) [,1] [,2] [,3] [1,] 0.29275003 0.70724967 -2.978356e-08 [2,] 0.29275015 0.70724997 1.232823e-08 [3,] -0.02233659 0.02233658 1.000000e+00 [,1] [1,] 131.81223 [2,] 131.81226 [3,] 36.37274 convertcolor2(rgb2,type="d",g=2.2) [,1] [,2] [,3] [1,] 0.29275003 0.70724967 -2.978356e-08 [2,] 0.29275015 0.70724997 1.232823e-08 [3,] -0.02233659 0.02233658 1.000000e+00 [,1] [1,] 122.71798 [2,] 122.71801 [3,] 48.34316
Cell Genomics cover
Our cover on the 11 January 2023 Cell Genomics issue depicts the process of determining the parent-of-origin using differential methylation of alleles at imprinted regions (iDMRs) is imagined as a circuit.
Designed in collaboration with with Carlos Urzua.
Akbari, V. et al. Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seq (2023) Cell Genomics 3(1).
Browse my gallery of cover designs.
Science Advances cover
My cover design on the 6 January 2023 Science Advances issue depicts DNA sequencing read translation in high-dimensional space. The image showss 672 bases of sequencing barcodes generated by three different single-cell RNA sequencing platforms were encoded as oriented triangles on the faces of three 7-dimensional cubes.
More details about the design.
Kijima, Y. et al. A universal sequencing read interpreter (2023) Science Advances 9
Browse my gallery of cover designs.
Regression modeling of time-to-event data with censoring
If you sit on the sofa for your entire life, you’re running a higher risk of getting heart disease and cancer. —Alex Honnold, American rock climber
In a follow-up to our Survival analysis — time-to-event data and censoring article, we look at how regression can be used to account for additional risk factors in survival analysis.
We explore accelerated failure time regression (AFTR) and the Cox Proportional Hazards model (Cox PH).
Dey, T., Lipsitz, S.R., Cooper, Z., Trinh, Q., Krzywinski, M & Altman, N. (2022) Points of significance: Regression modeling of time-to-event data with censoring. Nature Methods 19.
Music video for Max Cooper's Ascent
My 5-dimensional animation sets the visual stage for Max Cooper's Ascent from the album Unspoken Words. I have previously collaborated with Max on telling a story about infinity for his Yearning for the Infinite album.
I provide a walkthrough the video, describe the animation system I created to generate the frames, and show you all the keyframes
The video recently premiered on YouTube.
Renders of the full scene are available as NFTs.
Gene Cultures exhibit — art at the MIT Museum
I am more than my genome and my genome is more than me.
The MIT Museum reopened at its new location on 2nd October 2022. The new Gene Cultures exhibit featured my visualization of the human genome, which walks through the size and organization of the genome and some of the important structures.
