mirror of https://github.com/msberends/AMR.git
161 lines
8.0 KiB
Plaintext
Executable File
161 lines
8.0 KiB
Plaintext
Executable File
---
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title: "Benchmarks"
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author: "Matthijs S. Berends"
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date: '`r format(Sys.Date(), "%d %B %Y")`'
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output:
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rmarkdown::html_vignette:
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toc: true
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toc_depth: 3
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vignette: >
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%\VignetteIndexEntry{Benchmarks}
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%\VignetteEncoding{UTF-8}
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%\VignetteEngine{knitr::rmarkdown}
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editor_options:
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chunk_output_type: console
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---
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```{r setup, include = FALSE, results = 'markup'}
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knitr::opts_chunk$set(
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collapse = TRUE,
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comment = "#>",
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fig.width = 7.5,
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fig.height = 4.5
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)
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```
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One of the most important features of this package is the complete microbial taxonomic database, supplied by the Catalogue of Life (http://catalogueoflife.org). We created a function `as.mo()` that transforms any user input value to a valid microbial ID by using AI (Artificial Intelligence) combined with the taxonomic tree of Catalogue of Life.
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Using the `microbenchmark` package, we can review the calculation performance of this function. Its function `microbenchmark()` runs different input expressions independently of each other and measures their time-to-result.
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```{r, message = FALSE}
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library(microbenchmark)
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library(AMR)
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```
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In the next test, we try to 'coerce' different input values for *Staphylococcus aureus*. The actual result is the same every time: it returns its MO code `B_STPHY_AUR` (*B* stands for *Bacteria*, the taxonomic kingdom).
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But the calculation time differs a lot. Here, the AI effect can be reviewed best:
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```{r}
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S.aureus <- microbenchmark(as.mo("sau"),
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as.mo("stau"),
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as.mo("staaur"),
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as.mo("S. aureus"),
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as.mo("S. aureus"),
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as.mo("STAAUR"),
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as.mo("Staphylococcus aureus"),
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as.mo("B_STPHY_AUR"),
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times = 10)
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print(S.aureus, unit = "ms", signif = 3)
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```
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In the table above, all measurements are shown in milliseconds (thousands of seconds). A value of 10 milliseconds means it can determine 100 input values per second. It case of 50 milliseconds, this is only 20 input values per second. The more an input value resembles a full name, the faster the result will be found. In case of `as.mo("B_STPHY_AUR")`, the input is already a valid MO code, so it only almost takes no time at all (`r as.integer(min(S.aureus$time, na.rm = TRUE) / 1000)` millionths of seconds).
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To achieve this speed, the `as.mo` function also takes into account the prevalence of human pathogenic microorganisms. The downside is of course that less prevalent microorganisms will be determined less fast. See this example for the ID of *Mycoplasma leonicaptivi* (`B_MYCPL_LEO`), a bug probably never found before in humans:
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```{r}
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M.leonicaptivi <- microbenchmark(as.mo("myle"),
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as.mo("mycleo"),
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as.mo("M. leonicaptivi"),
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as.mo("M. leonicaptivi"),
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as.mo("MYCLEO"),
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as.mo("Mycoplasma leonicaptivi"),
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as.mo("B_MYCPL_LEO"),
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times = 10)
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print(M.leonicaptivi, unit = "ms", signif = 4)
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```
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That takes `r round(mean(M.leonicaptivi$time, na.rm = TRUE) / mean(S.aureus$time, na.rm = TRUE), 1)` times as much time on average! A value of 100 milliseconds means it can only determine ~10 different input values per second. We can conclude that looking up arbitrary codes of less prevalent microorganisms is the worst way to go, in terms of calculation performance:
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```{r}
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par(mar = c(5, 16, 4, 2)) # set more space for left margin text (16)
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# highest value on y axis
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max_y_axis <- max(S.aureus$time, M.leonicaptivi$time, na.rm = TRUE) / 1e6
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boxplot(S.aureus, horizontal = TRUE, las = 1, unit = "ms", log = FALSE, xlab = "", ylim = c(0, max_y_axis),
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main = expression(paste("Benchmark of ", italic("Staphylococcus aureus"))))
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boxplot(M.leonicaptivi, horizontal = TRUE, las = 1, unit = "ms", log = FALSE, xlab = "", ylim = c(0, max_y_axis),
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main = expression(paste("Benchmark of ", italic("Mycoplasma leonicaptivi"))))
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```
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To relieve this pitfall and further improve performance, two important calculations take almost no time at all: **repetitive results** and **already precalculated results**.
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### Repetitive results
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Repetitive results mean that unique values are present more than once. Unique values will only be calculated once by `as.mo()`. We will use `mo_fullname()` for this test - a helper function that returns the full microbial name (genus, species and possibly subspecies) which uses `as.mo()` internally.
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```{r, message = FALSE}
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library(dplyr)
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# take 500,000 random MO codes from the septic_patients data set
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x = septic_patients %>%
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sample_n(500000, replace = TRUE) %>%
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pull(mo)
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# got the right length?
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length(x)
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# and how many unique values do we have?
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n_distinct(x)
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# now let's see:
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run_it <- microbenchmark(mo_fullname(x),
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times = 10)
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print(run_it, unit = "ms", signif = 3)
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```
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So transforming 500,000 values (!) of `r n_distinct(x)` unique values only takes `r round(median(run_it$time, na.rm = TRUE) / 1e9, 2)` seconds (`r as.integer(median(run_it$time, na.rm = TRUE) / 1e6)` ms). You only lose time on your unique input values.
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### Precalculated results
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What about precalculated results? If the input is an already precalculated result of a helper function like `mo_fullname()`, it almost doesn't take any time at all (see 'C' below):
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```{r}
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run_it <- microbenchmark(A = mo_fullname("B_STPHY_AUR"),
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B = mo_fullname("S. aureus"),
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C = mo_fullname("Staphylococcus aureus"),
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times = 10)
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print(run_it, unit = "ms", signif = 3)
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```
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So going from `mo_fullname("Staphylococcus aureus")` to `"Staphylococcus aureus"` takes `r format(round(run_it %>% filter(expr == "C") %>% pull(time) %>% median() / 1e9, 4), scientific = FALSE)` seconds - it doesn't even start calculating *if the result would be the same as the expected resulting value*. That goes for all helper functions:
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```{r}
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run_it <- microbenchmark(A = mo_species("aureus"),
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B = mo_genus("Staphylococcus"),
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C = mo_fullname("Staphylococcus aureus"),
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D = mo_family("Staphylococcaceae"),
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E = mo_order("Bacillales"),
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F = mo_class("Bacilli"),
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G = mo_phylum("Firmicutes"),
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H = mo_kingdom("Bacteria"),
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times = 10)
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print(run_it, unit = "ms", signif = 3)
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```
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Of course, when running `mo_phylum("Firmicutes")` the function has zero knowledge about the actual microorganism, namely *S. aureus*. But since the result would be `"Firmicutes"` too, there is no point in calculating the result. And because this package 'knows' all phyla of all known bacteria (according to the Catalogue of Life), it can just return the initial value immediately.
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### Results in other languages
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When the system language is non-English and supported by this `AMR` package, some functions will have a translated result. This almost does't take extra time:
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```{r}
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mo_fullname("CoNS", language = "en") # or just mo_fullname("CoNS") on an English system
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mo_fullname("CoNS", language = "es") # or just mo_fullname("CoNS") on a Spanish system
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mo_fullname("CoNS", language = "nl") # or just mo_fullname("CoNS") on a Dutch system
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run_it <- microbenchmark(en = mo_fullname("CoNS", language = "en"),
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de = mo_fullname("CoNS", language = "de"),
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nl = mo_fullname("CoNS", language = "nl"),
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es = mo_fullname("CoNS", language = "es"),
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it = mo_fullname("CoNS", language = "it"),
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fr = mo_fullname("CoNS", language = "fr"),
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pt = mo_fullname("CoNS", language = "pt"),
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times = 10)
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print(run_it, unit = "ms", signif = 4)
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```
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Currently supported are German, Dutch, Spanish, Italian, French and Portuguese.
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