# Text embeddings

Text embeddings are particularly hot right now. While textmineR doesn’t (yet) explicitly implement any embedding models like GloVe or word2vec, you can still get embeddings. Text embedding algorithms aren’t conceptually different from topic models. They are, however, operating on a different matrix. Instead of reducing the dimensions of a document term matrix, text embeddings are obtained by reducing the dimensions of a term co-occurrence matrix. In principle, one can use LDA or LSA in the same way. In this case, rows of theta are embedded words. A phi_prime may be obtained to project documents or new text into the embedding space.

## Create a term co-occurrence matrix

The first step in fitting a text embedding model is to create a term co-occurrence matrix or TCM. In a TCM, both columns and rows index tokens. The $$(i,j)$$ entries of the matrix are a count of the number of times word $$i$$ co-occurs with $$j$$. However, there are several ways to count co-occurrence. textmineR gives you three.

The most useful way of counting co-occurrence for text embeddings is called the skip-gram model. Under the skip-gram model, the count would be the number of times word $$j$$ appears within a certain window of $$i$$. A skip-gram window of two, for example, would count the number of times word $$j$$ occurred in the two words immediately before word $$i$$ or the two words immediately after word $$i$$. This helps capture the local context of words. In fact, you can think of a text embedding as being a topic model based on the local context of words. Whereas a traditional topic model is modeling words in their global context.

To read more about the skip-gram model, which was popularized in the embedding model word2vec, look here.

The other types of co-occurrence matrix textmineR provides are both global. One is a count of the number of documents in which words $$i$$ and $$j$$ co-occur. The other is the number of terms that co-occur between documents $$i$$ and $$j$$. See help(CreateTcm) for info on these.


# load the NIH data set
library(textmineR)

# load nih_sample data set from textmineR
data(nih_sample)

# First create a TCM using skip grams, we'll use a 5-word window
# most options available on CreateDtm are also available for CreateTcm
tcm <- CreateTcm(doc_vec = nih_sample$ABSTRACT_TEXT, skipgram_window = 10, verbose = FALSE, cpus = 2) # a TCM is generally larger than a DTM dim(tcm) #> [1] 5210 5210 ## Fitting a model Once we have a TCM, we can use the same procedure to make an embedding model as we used to make a topic model. Note that it may take considerably longer (because of dimensionality of the matrix) or shorter (because of sparsity) to fit an embedding on the same corpus. # use LDA to get embeddings into probability space # This will take considerably longer as the TCM matrix has many more rows # than your average DTM embeddings <- FitLdaModel(dtm = tcm, k = 50, iterations = 200, burnin = 180, alpha = 0.1, beta = 0.05, optimize_alpha = TRUE, calc_likelihood = FALSE, calc_coherence = TRUE, calc_r2 = TRUE, cpus = 2) ## Interpretation of $$\Phi$$ and $$\Theta$$ In the language of text embeddings, $$\Theta$$ gives us our tokens embedded in a probability space (because we used LDA, Euclidean space if we used LSA). $$\Phi$$ defines the dimensions of our embedding space. The rows of $$\Phi$$ can still be interpreted as topics. But they are topics of local contexts, rather than within whole documents. ## Evaluating the model As it happens, the same evaluation metrics developed for topic modeling also apply here. There are subtle differences in interpretation because we are using a TCM not a DTM. i.e. occurrences relate words to each other, not to documents. # Get an R-squared for general goodness of fit embeddings$r2
#> [1] 0.1774482

# Get coherence (relative to the TCM) for goodness of fit
summary(embeddings$coherence) #> Min. 1st Qu. Median Mean 3rd Qu. Max. #> 0.01242 0.06924 0.10976 0.11906 0.15322 0.35695 We will create a summary table as we did with a topic model before. # Get top terms, no labels because we don't have bigrams embeddings$top_terms <- GetTopTerms(phi = embeddings$phi, M = 5) # Create a summary table, similar to the above embeddings$summary <- data.frame(topic = rownames(embeddings$phi), coherence = round(embeddings$coherence, 3),
prevalence = round(colSums(embeddings$theta), 2), top_terms = apply(embeddings$top_terms, 2, function(x){
paste(x, collapse = ", ")
}),
stringsAsFactors = FALSE)

Here it is ordered by prevalence. (Here, we might say density of tokens along each embedding dimension.)

embeddings$summary[ order(embeddings$summary$prevalence, decreasing = TRUE) , ][ 1:10 , ] Summary of top 10 embedding dimensions topic coherence prevalence top_terms t_9 t_9 0.154 184.30 research, health, cancer, clinical, core t_43 t_43 0.218 153.29 aim, specific, study, determine, studies t_46 t_46 0.193 151.00 cells, cell, brain, human, cancer t_42 t_42 0.136 134.75 program, core, support, national, investigators t_6 t_6 0.173 124.75 hiv, based, treatment, clinical, effect t_24 t_24 0.146 120.00 role, genetic, mechanisms, gene, expression t_45 t_45 0.136 113.39 data, studies, time, design, development t_7 t_7 0.118 112.90 factors, risk, early, sud, behavioral t_33 t_33 0.190 108.51 signaling, ri, mediated, fc, dependent t_39 t_39 0.147 107.31 response, immune, infection, proteins, sand And here is the table ordered by coherence. embeddings$summary[ order(embeddings$summary$coherence, decreasing = TRUE) , ][ 1:10 , ]
Summary of 10 most coherent embedding dimensions
topic coherence prevalence top_terms
t_22 t_22 0.357 95.64 race, fertility, ethnic, differences, unintended
t_3 t_3 0.284 100.41 microbiome, gut, crc, composition, bas
t_34 t_34 0.259 100.42 secondary, ptc, brafv, drug, primary
t_50 t_50 0.221 104.79 sleep, cdk, memory, dependent, activity
t_43 t_43 0.218 153.29 aim, specific, study, determine, studies
t_35 t_35 0.212 100.74 mice, injury, cmybp, blood, fragment
t_46 t_46 0.193 151.00 cells, cell, brain, human, cancer
t_33 t_33 0.190 108.51 signaling, ri, mediated, fc, dependent
t_23 t_23 0.189 98.87 lung, ipf, behavior, patients, expression
t_26 t_26 0.182 97.91 metabolic, mitochondrial, secretion, bde, redox

## Embedding documents under the model

You can embed whole documents under your model. Doing so, effectively makes your embeddings a topic model that have topics of local contexts, instead of global ones. Why might you want to do this? The short answer is that you may have reason to believe that an embedding model may give you better topics, especially if you are trying to pick up on more subtle topics. In a later example, we’ll be doing that to build a document summarizer.

A note on the below: TCMs may be very sparse and cause us to run into computational underflow issues when using the “gibbs” prediction method. As a result, I’m choosing to use the “dot” method.

# Make a DTM from our documents
dtm_embed <- CreateDtm(doc_vec = nih_sample$ABSTRACT_TEXT, doc_names = nih_sample$APPLICATION_ID,
ngram_window = c(1,1),
verbose = FALSE,
cpus = 2)

dtm_embed <- dtm_embed[,colSums(dtm_embed) > 2]

# Project the documents into the embedding space
embedding_assignments <- predict(embeddings, dtm_embed, method = "gibbs",
iterations = 200, burnin = 180)

Once you’ve embedded your documents, you effectively have a new $$\Theta$$. We can use that to evaluate how well the embedding topics fit the documents as a whole by re-calculating R-squared and coherence.

# get a goodness of fit relative to the DTM
embeddings$r2_dtm <- CalcTopicModelR2(dtm = dtm_embed, phi = embeddings$phi[,colnames(dtm_embed)], # line up vocabulary
theta = embedding_assignments,
cpus = 2)

embeddings$r2_dtm #> [1] 0.2134098 # get coherence relative to DTM embeddings$coherence_dtm <- CalcProbCoherence(phi = embeddings$phi[,colnames(dtm_embed)], # line up vocabulary dtm = dtm_embed) summary(embeddings$coherence_dtm)
#>     Min.  1st Qu.   Median     Mean  3rd Qu.     Max.
#> -0.01454  0.03715  0.08847  0.12319  0.17537  0.52295

## Where to next?

Embedding research is only just beginning. I would encourage you to play with them and develop your own methods.