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zaomm

I want to diverge from my traditional scope of topics and propose a new benchmark for weightlifting and CrossFit: the `k` index.

The `k` index is brainy and fun and gives you a new way to structure your goals. At high values, it's very hard to increase, making each increment a huge challenge.

Going around with a t-shirt that says "`k=40` at everything" is maximally geeky and athletic.

For a given movement (e.g. squat, deadlift, press), you achieve index rank `k` if you can perform `k` unbroken reps at `k`% of your current one rep max (1RM).

Unbroken means no more than 1–2 seconds of pause between each rep. Exact standards would need to be established for competition.

Suppose an athlete's one rep max (1RM) squat is 100 kg (220 lb).

The athlete will have a `k` index rating of `k=10` for squats if they can perform 10 unbroken reps at 10% 1RM, which is 10 kg (22 lb).

The athlete will have a `k` index rating of `k=20` for squats if they can perform 20 unbroken reps at 20% 1RM, which is 20 kg (44 lb).

The athlete will have an independent `k` index rating for other movements like deadlift and press. These ratings are likely to be different for each movement.

The minimum `k` index is `k=0` and it's a value we're born with.

The maximum theoretical `k` index is trivially `k=100` because, by definition, you cannot lift more than your current 1RM.

The maximum practical `k` index is much lower than `k=100` and probably in the range of `k = 50`.

If you perform `r` reps at weight `w` you can estimate your 1RM using the Epley formula `w(1+r/30)` assuming `r>1`. In other words, for each rep at a weight `w` your estimate of your 1RM increases by ~3.3% above `w`.

There are various 1RM estimate equations and generally they are designed for fewer than 20 reps.

In some estimates, like by Mayhew et al. and by Wathan, the rep counts appear as `e^{-xr}` for small `x` such as `x=0.055` which makes the formula converge to a value when `r` is large like `r>15`. For example, Mayhew et al. converges to to a maximum of 1.91× of the weight being tested and Wathan converges to 2.05× of the weight being tested.

Other estimates, like McGlothin, generate unreasonable values for high rep count (e.g. 185 lb at 25 reps suggests a 1RM of 535 lb, which is insanely high) and for `r>37` gives negative estimates.

Therefore, while I'm reluctant to apply any of these equations to get a rough idea of an expected `k` value, I'm going to go ahead any way and use the Epley formula.

But let's try it anyway. If you lift `k` reps at `k`% 1RM and we assume Epley applies, $$ k/100 * 1RM * (1+k/30) = 1RM $$

which gives `k` to the nearest rep $$ k = 41 $$

Again, if Epley applies (which it probably doesn't), this means that if your `k > 41` you have more endurance relative to your level of strength.

Similarly, if your `k < 41` then your strength is higher relative to your level of endurance.

In the table below I provide the 1RM estimate for each `k` index value, which should give you an idea of how difficult it is to increase the `k` index.

From personal experience—I haven't tried this yet—achieving `k=30` is going to be hard and `k=40` feels to me like it would be extremely challenging.

The `k` index requires more preparation and thought than testing your 1RM.

To accurately assess your `k` index you need to first have an accurate assessment of your 1RM. Thus, a proper 1RM test is a prerequisite.

Second, you need to pick a value of `k` to attempt to achieve and then attempt to perform the `k` reps at the required weight. If this is your first `k` index test, you need to pick `k` conservatively.

I suggest trying for `k=20` (20 reps at 20% 1RM). This should be doable for most people. Depending on how the 20th rep felt, you might want to take a 5 min rest and then try for `k=25` (25 reps at 25% 1RM). This should be exponentially harder than testing for `k=20`.

Everytime you retest your 1RM you need to retest your `k` index.

The `k` index is a measure of muscle endurance and movement efficiency.

It is not a measure of raw strength, since it is not strictly a function of your 1RM—an athelete with a lower 1RM may have a higher `k` index for that movement.

It attempts to simplify multi-rep benchmarks like 3RM, 5RM, 10RM and so on. Although these themselves are very useful and I would not advocate forgetting about them, the `k` index adds a measure of grit into the mix.

As a single number, the `k` index can be used to visualize performance, especially in combination with 1RM. A plot of `k` vs 1RM would very nicely distinguish different training regimes, such as powerlifting (low `k` high 1RM) and CrossFit (high `k` lower 1RM).

Your `k` index may change independently of your 1RM, or vice versa. For example, you can get stronger and increase your 1RM but now find that your `k` index is lower.

I think most people can get `k=20`, or close to it, on their first try. The range between `k=30` and `k=50` is where things get interesting and very painful.

The `k` index is similar to the *h* index, a metric commonly used in academic publishing.

The *h* index is defined as follows. "A scholar with an index of `h` has published `h` papers each of which has been cited in other papers at least `h` times.". For example, if I have an `h=10` then I have 10 papers that have at least 10 citations each.

To increase my `h` index to 11, it is not enough to publish a paper with 11 citations. Now, the other 10 papers also have to have an extra citation each.

In 1 hour, establish your `k` index for squats, deadlift and strict press, in that order. The total of your `k` index values is your `k` total.

Beginner athletes: attempt `k=20`, `k=24` and `k=27`.

Intermediate athletes: attempt `k=24`, `k=27` and `k=30`.

Elite athletes: attempt `k=30`, `k=32` and `k=34`.

The goal of this workout is to test all three `k` indexes in one session. You can test the individual movements on separate days and compare.

The `k` index is only applicable for movements in which an athelete moves weight and for which a 1RM can be measured.

It does not apply to body weight movements like unweighted pushups or pullups. It can, however, apply to weighted forms of those movements.

Achieving the same `k` index for different movements may not be equally easy. For example, it's probably easier to have a `k=30` for deadlift than for strict press, since the latter uses smaller muscles.

All of the following are equivalent.

squat `k30`

`k30` (squat)

squat `k=30`

A squat `k` index of 30.

The table below shows the requirement for achieving each index assuming a 1RM of 100 kg.

The performance column gives the 1RM estimate using the Epley formula based on your rep count relative to the actual 1RM used to calculate the weight. For example, for `k=30` your 1RM estimate is `30/100 * (1+30/30) = 0.6` of your 1RM, which is lower than you estimated and you can said to be underperforming. On the other hand, if you manage `k=50` then your 1RM estimate based on your rep scheme is 1.33× the value used to calculate the weight.

As I mentioned above, the use of the Epley formula here is almost definitely wrong. However, I haven't done enough research in this field to know what formula to use for accurate 1RM estimation from a very high rep count. It's possible that no such accurate assessment can be made and I need to try to at least try it for myself in the gym.

k | reps | performance |
---|---|---|

1 | 1 @ 1% 1RM (1 kg) | 0.01 |

2 | 2 @ 2% 1RM (2 kg) | 0.02 |

3 | 3 @ 3% 1RM (3 kg) | 0.03 |

4 | 4 @ 4% 1RM (4 kg) | 0.05 |

5 | 5 @ 5% 1RM (5 kg) | 0.06 |

6 | 6 @ 6% 1RM (6 kg) | 0.07 |

7 | 7 @ 7% 1RM (7 kg) | 0.09 |

8 | 8 @ 8% 1RM (8 kg) | 0.10 |

9 | 9 @ 9% 1RM (9 kg) | 0.12 |

10 | 10 @ 10% 1RM (10 kg) | 0.13 |

11 | 11 @ 11% 1RM (11 kg) | 0.15 |

12 | 12 @ 12% 1RM (12 kg) | 0.17 |

13 | 13 @ 13% 1RM (13 kg) | 0.19 |

14 | 14 @ 14% 1RM (14 kg) | 0.21 |

15 | 15 @ 15% 1RM (15 kg) | 0.22 |

16 | 16 @ 16% 1RM (16 kg) | 0.25 |

17 | 17 @ 17% 1RM (17 kg) | 0.27 |

18 | 18 @ 18% 1RM (18 kg) | 0.29 |

19 | 19 @ 19% 1RM (19 kg) | 0.31 |

20 | 20 @ 20% 1RM (20 kg) | 0.33 |

21 | 21 @ 21% 1RM (21 kg) | 0.36 |

22 | 22 @ 22% 1RM (22 kg) | 0.38 |

23 | 23 @ 23% 1RM (23 kg) | 0.41 |

24 | 24 @ 24% 1RM (24 kg) | 0.43 |

25 | 25 @ 25% 1RM (25 kg) | 0.46 |

26 | 26 @ 26% 1RM (26 kg) | 0.49 |

27 | 27 @ 27% 1RM (27 kg) | 0.51 |

28 | 28 @ 28% 1RM (28 kg) | 0.54 |

29 | 29 @ 29% 1RM (29 kg) | 0.57 |

30 | 30 @ 30% 1RM (30 kg) | 0.60 |

31 | 31 @ 31% 1RM (31 kg) | 0.63 |

32 | 32 @ 32% 1RM (32 kg) | 0.66 |

33 | 33 @ 33% 1RM (33 kg) | 0.69 |

34 | 34 @ 34% 1RM (34 kg) | 0.73 |

35 | 35 @ 35% 1RM (35 kg) | 0.76 |

36 | 36 @ 36% 1RM (36 kg) | 0.79 |

37 | 37 @ 37% 1RM (37 kg) | 0.83 |

38 | 38 @ 38% 1RM (38 kg) | 0.86 |

39 | 39 @ 39% 1RM (39 kg) | 0.90 |

40 | 40 @ 40% 1RM (40 kg) | 0.93 |

41 | 41 @ 41% 1RM (41 kg) | 0.97 |

42 | 42 @ 42% 1RM (42 kg) | 1.01 |

43 | 43 @ 43% 1RM (43 kg) | 1.05 |

44 | 44 @ 44% 1RM (44 kg) | 1.09 |

45 | 45 @ 45% 1RM (45 kg) | 1.12 |

46 | 46 @ 46% 1RM (46 kg) | 1.17 |

47 | 47 @ 47% 1RM (47 kg) | 1.21 |

48 | 48 @ 48% 1RM (48 kg) | 1.25 |

49 | 49 @ 49% 1RM (49 kg) | 1.29 |

50 | 50 @ 50% 1RM (50 kg) | 1.33 |

k | reps | performance |
---|---|---|

51 | 51 @ 51% 1RM (51 kg) | 1.38 |

52 | 52 @ 52% 1RM (52 kg) | 1.42 |

53 | 53 @ 53% 1RM (53 kg) | 1.47 |

54 | 54 @ 54% 1RM (54 kg) | 1.51 |

55 | 55 @ 55% 1RM (55 kg) | 1.56 |

56 | 56 @ 56% 1RM (56 kg) | 1.61 |

57 | 57 @ 57% 1RM (57 kg) | 1.65 |

58 | 58 @ 58% 1RM (58 kg) | 1.70 |

59 | 59 @ 59% 1RM (59 kg) | 1.75 |

60 | 60 @ 60% 1RM (60 kg) | 1.80 |

61 | 61 @ 61% 1RM (61 kg) | 1.85 |

62 | 62 @ 62% 1RM (62 kg) | 1.90 |

63 | 63 @ 63% 1RM (63 kg) | 1.95 |

64 | 64 @ 64% 1RM (64 kg) | 2.01 |

65 | 65 @ 65% 1RM (65 kg) | 2.06 |

66 | 66 @ 66% 1RM (66 kg) | 2.11 |

67 | 67 @ 67% 1RM (67 kg) | 2.17 |

68 | 68 @ 68% 1RM (68 kg) | 2.22 |

69 | 69 @ 69% 1RM (69 kg) | 2.28 |

70 | 70 @ 70% 1RM (70 kg) | 2.33 |

71 | 71 @ 71% 1RM (71 kg) | 2.39 |

72 | 72 @ 72% 1RM (72 kg) | 2.45 |

73 | 73 @ 73% 1RM (73 kg) | 2.51 |

74 | 74 @ 74% 1RM (74 kg) | 2.57 |

75 | 75 @ 75% 1RM (75 kg) | 2.62 |

76 | 76 @ 76% 1RM (76 kg) | 2.69 |

77 | 77 @ 77% 1RM (77 kg) | 2.75 |

78 | 78 @ 78% 1RM (78 kg) | 2.81 |

79 | 79 @ 79% 1RM (79 kg) | 2.87 |

80 | 80 @ 80% 1RM (80 kg) | 2.93 |

81 | 81 @ 81% 1RM (81 kg) | 3.00 |

82 | 82 @ 82% 1RM (82 kg) | 3.06 |

83 | 83 @ 83% 1RM (83 kg) | 3.13 |

84 | 84 @ 84% 1RM (84 kg) | 3.19 |

85 | 85 @ 85% 1RM (85 kg) | 3.26 |

86 | 86 @ 86% 1RM (86 kg) | 3.33 |

87 | 87 @ 87% 1RM (87 kg) | 3.39 |

88 | 88 @ 88% 1RM (88 kg) | 3.46 |

89 | 89 @ 89% 1RM (89 kg) | 3.53 |

90 | 90 @ 90% 1RM (90 kg) | 3.60 |

91 | 91 @ 91% 1RM (91 kg) | 3.67 |

92 | 92 @ 92% 1RM (92 kg) | 3.74 |

93 | 93 @ 93% 1RM (93 kg) | 3.81 |

94 | 94 @ 94% 1RM (94 kg) | 3.89 |

95 | 95 @ 95% 1RM (95 kg) | 3.96 |

96 | 96 @ 96% 1RM (96 kg) | 4.03 |

97 | 97 @ 97% 1RM (97 kg) | 4.11 |

98 | 98 @ 98% 1RM (98 kg) | 4.18 |

99 | 99 @ 99% 1RM (99 kg) | 4.26 |

100 | 100 @ 100% 1RM (100 kg) | 4.33 |

news
**+** thoughts

*Nature is often hidden, sometimes overcome, seldom extinguished. —Francis Bacon*

In the first of a series of columns about neural networks, we introduce them with an intuitive approach that draws from our discussion about logistic regression.

Simple neural networks are just a chain of linear regressions. And, although neural network models can get very complicated, their essence can be understood in terms of relatively basic principles.

We show how neural network components (neurons) can be arranged in the network and discuss the ideas of hidden layers. Using a simple data set we show how even a 3-neuron neural network can already model relatively complicated data patterns.

Derry, A., Krzywinski, M & Altman, N. (2023) Points of significance: Neural network primer. *Nature Methods* **20**.

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

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.

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.

*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**.

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.

*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.

© 1999–2023 Martin Krzywinski | contact | Canada's Michael Smith Genome Sciences Centre ⊂ BC Cancer Research Center ⊂ BC Cancer ⊂ PHSA