Scientific publication
T. M. Lange, M. Gültas, A. O. Schmitt & F. Heinrich (2025). optRF: Optimising random forest stability by figuring out the optimum variety of bushes. BMC bioinformatics, 26(1), 95.
Comply with this LINK to the unique publication.
Forest — A Highly effective Software for Anybody Working With Knowledge
What’s Random Forest?
Have you ever ever wished you may make higher selections utilizing knowledge — like predicting the chance of illnesses, crop yields, or recognizing patterns in buyer conduct? That’s the place machine studying is available in and some of the accessible and highly effective instruments on this subject is one thing known as Random Forest.
So why is random forest so widespread? For one, it’s extremely versatile. It really works effectively with many sorts of knowledge whether or not numbers, classes, or each. It’s additionally broadly utilized in many fields — from predicting affected person outcomes in healthcare to detecting fraud in finance, from bettering buying experiences on-line to optimising agricultural practices.
Regardless of the identify, random forest has nothing to do with bushes in a forest — but it surely does use one thing known as Choice Bushes to make sensible predictions. You possibly can consider a choice tree as a flowchart that guides a sequence of sure/no questions based mostly on the information you give it. A random forest creates a complete bunch of those bushes (therefore the “forest”), every barely totally different, after which combines their outcomes to make one last resolution. It’s a bit like asking a bunch of specialists for his or her opinion after which going with the bulk vote.
However till just lately, one query was unanswered: What number of resolution bushes do I really need? If every resolution tree can result in totally different outcomes, averaging many bushes would result in higher and extra dependable outcomes. However what number of are sufficient? Fortunately, the optRF package deal solutions this query!
So let’s take a look at tips on how to optimise Random Forest for predictions and variable choice!
Making Predictions with Random Forests
To optimise and to make use of random forest for making predictions, we are able to use the open-source statistics programme R. As soon as we open R, we’ve got to put in the 2 R packages “ranger” which permits to make use of random forests in R and “optRF” to optimise random forests. Each packages are open-source and accessible through the official R repository CRAN. To be able to set up and cargo these packages, the next traces of R code could be run:
> set up.packages(“ranger”)
> set up.packages(“optRF”)
> library(ranger)
> library(optRF)
Now that the packages are put in and loaded into the library, we are able to use the capabilities that these packages comprise. Moreover, we are able to additionally use the information set included within the optRF package deal which is free to make use of below the GPL license (simply because the optRF package deal itself). This knowledge set known as SNPdata comprises within the first column the yield of 250 wheat crops in addition to 5000 genomic markers (so known as single nucleotide polymorphisms or SNPs) that may comprise both the worth 0 or 2.
> SNPdata[1:5,1:5]
Yield SNP_0001 SNP_0002 SNP_0003 SNP_0004
ID_001 670.7588 0 0 0 0
ID_002 542.5611 0 2 0 0
ID_003 591.6631 2 2 0 2
ID_004 476.3727 0 0 0 0
ID_005 635.9814 2 2 0 2
This knowledge set is an instance for genomic knowledge and can be utilized for genomic prediction which is a vital instrument for breeding high-yielding crops and, thus, to battle world starvation. The concept is to foretell the yield of crops utilizing genomic markers. And precisely for this goal, random forest can be utilized! That implies that a random forest mannequin is used to explain the connection between the yield and the genomic markers. Afterwards, we are able to predict the yield of wheat crops the place we solely have genomic markers.
Subsequently, let’s think about that we’ve got 200 wheat crops the place we all know the yield and the genomic markers. That is the so-called coaching knowledge set. Let’s additional assume that we’ve got 50 wheat crops the place we all know the genomic markers however not their yield. That is the so-called check knowledge set. Thus, we separate the information body SNPdata in order that the primary 200 rows are saved as coaching and the final 50 rows with out their yield are saved as check knowledge:
> Coaching = SNPdata[1:200,]
> Check = SNPdata[201:250,-1]
With these knowledge units, we are able to now take a look at tips on how to make predictions utilizing random forests!
First, we acquired to calculate the optimum variety of bushes for random forest. Since we wish to make predictions, we use the operate opt_prediction
from the optRF package deal. Into this operate we’ve got to insert the response from the coaching knowledge set (on this case the yield), the predictors from the coaching knowledge set (on this case the genomic markers), and the predictors from the check knowledge set. Earlier than we run this operate, we are able to use the set.seed operate to make sure reproducibility despite the fact that this isn’t essential (we’ll see later why reproducibility is a matter right here):
> set.seed(123)
> optRF_result = opt_prediction(y = Coaching[,1],
+ X = Coaching[,-1],
+ X_Test = Check)
Beneficial variety of bushes: 19000
All the outcomes from the opt_prediction
operate are actually saved within the object optRF_result, nonetheless, an important data was already printed within the console: For this knowledge set, we must always use 19,000 bushes.
With this data, we are able to now use random forest to make predictions. Subsequently, we use the ranger operate to derive a random forest mannequin that describes the connection between the genomic markers and the yield within the coaching knowledge set. Additionally right here, we’ve got to insert the response within the y argument and the predictors within the x argument. Moreover, we are able to set the write.forest
argument to be TRUE and we are able to insert the optimum variety of bushes within the num.bushes
argument:
> RF_model = ranger(y = Coaching[,1], x = Coaching[,-1],
+ write.forest = TRUE, num.bushes = 19000)
And that’s it! The thing RF_model
comprises the random forest mannequin that describes the connection between the genomic markers and the yield. With this mannequin, we are able to now predict the yield for the 50 crops within the check knowledge set the place we’ve got the genomic markers however we don’t know the yield:
> predictions = predict(RF_model, knowledge=Check)$predictions
> predicted_Test = knowledge.body(ID = row.names(Check), predicted_yield = predictions)
The info body predicted_Test now comprises the IDs of the wheat crops along with their predicted yield:
> head(predicted_Test)
ID predicted_yield
ID_201 593.6063
ID_202 596.8615
ID_203 591.3695
ID_204 589.3909
ID_205 599.5155
ID_206 608.1031
Variable Choice with Random Forests
A distinct strategy to analysing such a knowledge set can be to seek out out which variables are most vital to foretell the response. On this case, the query can be which genomic markers are most vital to foretell the yield. Additionally this may be performed with random forests!
If we sort out such a process, we don’t want a coaching and a check knowledge set. We are able to merely use the whole knowledge set SNPdata and see which of the variables are an important ones. However earlier than we try this, we must always once more decide the optimum variety of bushes utilizing the optRF package deal. Since we’re insterested in calculating the variable significance, we use the operate opt_importance
:
> set.seed(123)
> optRF_result = opt_importance(y=SNPdata[,1],
+ X=SNPdata[,-1])
Beneficial variety of bushes: 40000
One can see that the optimum variety of bushes is now greater than it was for predictions. That is really usually the case. Nevertheless, with this variety of bushes, we are able to now use the ranger operate to calculate the significance of the variables. Subsequently, we use the ranger operate as earlier than however we alter the variety of bushes within the num.bushes argument to 40,000 and we set the significance argument to “permutation” (different choices are “impurity” and “impurity_corrected”).
> set.seed(123)
> RF_model = ranger(y=SNPdata[,1], x=SNPdata[,-1],
+ write.forest = TRUE, num.bushes = 40000,
+ significance="permutation")
> D_VI = knowledge.body(variable = names(SNPdata)[-1],
+ significance = RF_model$variable.significance)
> D_VI = D_VI[order(D_VI$importance, decreasing=TRUE),]
The info body D_VI now comprises all of the variables, thus, all of the genomic markers, and subsequent to it, their significance. Additionally, we’ve got immediately ordered this knowledge body in order that an important markers are on the highest and the least vital markers are on the backside of this knowledge body. Which implies that we are able to take a look at an important variables utilizing the pinnacle operate:
> head(D_VI)
variable significance
SNP_0020 45.75302
SNP_0004 38.65594
SNP_0019 36.81254
SNP_0050 34.56292
SNP_0033 30.47347
SNP_0043 28.54312
And that’s it! We now have used random forest to make predictions and to estimate an important variables in a knowledge set. Moreover, we’ve got optimised random forest utilizing the optRF package deal!
Why Do We Want Optimisation?
Now that we’ve seen how simple it’s to make use of random forest and the way shortly it may be optimised, it’s time to take a more in-depth take a look at what’s occurring behind the scenes. Particularly, we’ll discover how random forest works and why the outcomes may change from one run to a different.
To do that, we’ll use random forest to calculate the significance of every genomic marker however as an alternative of optimising the variety of bushes beforehand, we’ll stick to the default settings within the ranger operate. By default, ranger makes use of 500 resolution bushes. Let’s strive it out:
> set.seed(123)
> RF_model = ranger(y=SNPdata[,1], x=SNPdata[,-1],
+ write.forest = TRUE, significance="permutation")
> D_VI = knowledge.body(variable = names(SNPdata)[-1],
+ significance = RF_model$variable.significance)
> D_VI = D_VI[order(D_VI$importance, decreasing=TRUE),]
> head(D_VI)
variable significance
SNP_0020 80.22909
SNP_0019 60.37387
SNP_0043 50.52367
SNP_0005 43.47999
SNP_0034 38.52494
SNP_0015 34.88654
As anticipated, the whole lot runs easily — and shortly! The truth is, this run was considerably quicker than after we beforehand used 40,000 bushes. However what occurs if we run the very same code once more however this time with a distinct seed?
> set.seed(321)
> RF_model2 = ranger(y=SNPdata[,1], x=SNPdata[,-1],
+ write.forest = TRUE, significance="permutation")
> D_VI2 = knowledge.body(variable = names(SNPdata)[-1],
+ significance = RF_model2$variable.significance)
> D_VI2 = D_VI2[order(D_VI2$importance, decreasing=TRUE),]
> head(D_VI2)
variable significance
SNP_0050 60.64051
SNP_0043 58.59175
SNP_0033 52.15701
SNP_0020 51.10561
SNP_0015 34.86162
SNP_0019 34.21317
As soon as once more, the whole lot seems to work tremendous however take a more in-depth take a look at the outcomes. Within the first run, SNP_0020 had the best significance rating at 80.23, however within the second run, SNP_0050 takes the highest spot and SNP_0020 drops to the fourth place with a a lot decrease significance rating of 51.11. That’s a major shift! So what modified?
The reply lies in one thing known as non-determinism. Random forest, because the identify suggests, includes a whole lot of randomness: it randomly selects knowledge samples and subsets of variables at numerous factors throughout coaching. This randomness helps forestall overfitting but it surely additionally implies that outcomes can range barely every time you run the algorithm — even with the very same knowledge set. That’s the place the set.seed() operate is available in. It acts like a bookmark in a shuffled deck of playing cards. By setting the identical seed, you make sure that the random decisions made by the algorithm observe the identical sequence each time you run the code. However once you change the seed, you’re successfully altering the random path the algorithm follows. That’s why, in our instance, an important genomic markers got here out otherwise in every run. This conduct — the place the identical course of can yield totally different outcomes attributable to inside randomness — is a traditional instance of non-determinism in machine studying.

As we simply noticed, random forest fashions can produce barely totally different outcomes each time you run them even when utilizing the identical knowledge as a result of algorithm’s built-in randomness. So, how can we cut back this randomness and make our outcomes extra steady?
One of many easiest and handiest methods is to extend the variety of bushes. Every tree in a random forest is educated on a random subset of the information and variables, so the extra bushes we add, the higher the mannequin can “common out” the noise brought on by particular person bushes. Consider it like asking 10 individuals for his or her opinion versus asking 1,000 — you’re extra prone to get a dependable reply from the bigger group.
With extra bushes, the mannequin’s predictions and variable significance rankings are inclined to change into extra steady and reproducible even with out setting a particular seed. In different phrases, including extra bushes helps to tame the randomness. Nevertheless, there’s a catch. Extra bushes additionally imply extra computation time. Coaching a random forest with 500 bushes may take a number of seconds however coaching one with 40,000 bushes might take a number of minutes or extra, relying on the dimensions of your knowledge set and your pc’s efficiency.
Nevertheless, the connection between the soundness and the computation time of random forest is non-linear. Whereas going from 500 to 1,000 bushes can considerably enhance stability, going from 5,000 to 10,000 bushes may solely present a tiny enchancment in stability whereas doubling the computation time. In some unspecified time in the future, you hit a plateau the place including extra bushes provides diminishing returns — you pay extra in computation time however achieve little or no in stability. That’s why it’s important to seek out the best stability: Sufficient bushes to make sure steady outcomes however not so many who your evaluation turns into unnecessarily gradual.
And that is precisely what the optRF package deal does: it analyses the connection between the soundness and the variety of bushes in random forests and makes use of this relationship to find out the optimum variety of bushes that results in steady outcomes and past which including extra bushes would unnecessarily enhance the computation time.
Above, we’ve got already used the opt_importance operate and saved the outcomes as optRF_result. This object comprises the details about the optimum variety of bushes but it surely additionally comprises details about the connection between the soundness and the variety of bushes. Utilizing the plot_stability operate, we are able to visualise this relationship. Subsequently, we’ve got to insert the identify of the optRF object, which measure we’re serious about (right here, we have an interest within the “significance”), the interval we wish to visualise on the X axis, and if the advisable variety of bushes must be added:
> plot_stability(optRF_result, measure="significance",
+ from=0, to=50000, add_recommendation=FALSE)

This plot clearly reveals the non-linear relationship between stability and the variety of bushes. With 500 bushes, random forest solely results in a stability of round 0.2 which explains why the outcomes modified drastically when repeating random forest after setting a distinct seed. With the advisable 40,000 bushes, nonetheless, the soundness is close to 1 (which signifies an ideal stability). Including greater than 40,000 bushes would get the soundness additional to 1 however this enhance can be solely very small whereas the computation time would additional enhance. That’s the reason 40,000 bushes point out the optimum variety of bushes for this knowledge set.
The Takeaway: Optimise Random Forest to Get the Most of It
Random forest is a robust ally for anybody working with knowledge — whether or not you’re a researcher, analyst, pupil, or knowledge scientist. It’s simple to make use of, remarkably versatile, and extremely efficient throughout a variety of purposes. However like all instrument, utilizing it effectively means understanding what’s occurring below the hood. On this submit, we’ve uncovered considered one of its hidden quirks: The randomness that makes it robust may make it unstable if not fastidiously managed. Fortuitously, with the optRF package deal, we are able to strike the right stability between stability and efficiency, making certain we get dependable outcomes with out losing computational sources. Whether or not you’re working in genomics, medication, economics, agriculture, or some other data-rich subject, mastering this stability will aid you make smarter, extra assured selections based mostly in your knowledge.