# Distributed Analysis of the Origin of the Human Immunodeficiency Virus

This example shows how the Parallel Computing Toolbox™ can be used to perform pairwise sequence alignment (PWSA). PWSA has multiple applications in bioinformatics, such as multiple sequence analysis and phylogenetic tree reconstruction. We look at a PWSA that uses a global dynamic programming algorithm to align each pair of sequences, and we then calculate the pairwise distances using the Tajima-Nei metric. This gives us a matrix of distances between sequences that we use for inferring the phylogeny of HIV and SIV viruses. PWSA is a computationally expensive task with complexity O(L*L*N*N), where L is the average length of the sequences and N is the number of sequences [Durbin, et al. Cambridge University Press, 1998].

For details about the computations, view the code for pctdemo_setup_hiv.

Prerequisites:

Related examples:

## Contents

## Analyze the Sequential Problem

First, we look at how the computations in the sequential example fit into the model introduced in the Dividing MATLAB Computations into Tasks example. The call to `seqpdist` is the most computationally intensive part of the sequential example, and it basically performs the following parameter sweep:

for all pairs (s1, s2) formed from the elements of seq distance(s1, s2) = seqpdist(s1, s2); end

The distance is, of course, symmetric, i.e., `seqpdist(s1, s2) = seqpdist(s2, s1)`. Because `seqpdist` re-normalizes the distances based on the entire input sequence `seq`, we have to calculate that renormalization factor ourselves in this example, and we also need to identify the pairs between which to measure the distance.

Since we calculate a rather large number of distances, we have each task calculate several distances. This requires us to write a simple wrapper task function that invokes `seqpdist`.

## Load the Example Settings and the Data

The example uses the default profile when identifying the cluster to use. The profiles documentation explains how to create new profiles and how to change the default profile. See Customizing the Settings for the Examples in the Parallel Computing Toolbox for instructions on how to change the example difficulty level or the number of tasks created.

[difficulty, myCluster, numTasks] = pctdemo_helper_getDefaults();

The `pctdemo_setup_hiv` function retrieves the protein sequence information from the NCBI GenBank® database, and the `difficulty` parameter controls how many protein sequences we retrieve. You can view the code for pctdemo_setup_hiv for full details.

[fig, pol, description] = pctdemo_setup_hiv(difficulty); numViruses = length(pol); startTime = clock;

Downloading data from the NCBI GenBank database Finished downloading

## Divide the Work into Smaller Tasks

We use the Tajima-Nei method to measure the distance between the POL coding regions. Tajima-Nei distances are based on the frequency of nucleotides in the whole group of sequences. When you call `seqpdist` for only two sequences, the function would compute the nucleotide count based on only the two sequences and not on the whole group. Consequently, we calculate the frequency based on the whole group and pass that information to `seqpdist`.

bc = basecount(strcat(pol.Sequence)); bf = [bc.A bc.C bc.G bc.T]/(bc.A + bc.C + bc.G + bc.T);

Let's find the parameter space that we want to traverse. The `seqpdist` documentation gives us useful information in this regard:

% D = SEQPDIST(SEQS) returns a vector D containing biological distances % between each pair of sequences stored in the M elements of the cell % SEQS. D is an (M*(M-1)/2)-by-1 vector, corresponding to the M*(M-1)/2 % pairs of sequences in SEQS. The output D is arranged in the order of % ((2,1),(3,1),..., (M,1),(3,2),...(M,2),.....(M,M-1), i.e., the lower % left triangle of the full M-by-M distance matrix.

Based on this information, we create two vectors, `Aseq` and `Bseq`, that contain the sequence pairs between which to calculate the distances.

Aseq = struct; Bseq = struct; ind = 1; for j = 1:numViruses for i = j+1:numViruses Aseq(ind).Sequence = pol(j).Sequence; Bseq(ind).Sequence = pol(i).Sequence; ind = ind + 1; end end

We want to divide the vectors `Asplit` and `Bsplit` between the tasks.

[Asplit, numTasks] = pctdemo_helper_split_vector(Aseq, numTasks); Bsplit = pctdemo_helper_split_vector(Bseq, numTasks); fprintf(['This example will submit a job with %d task(s) ' ... 'to the cluster.\n'], numTasks);

This example will submit a job with 4 task s to the cluster.

## Create and Submit the Job

We create a job and the tasks in the job. Task `i` calculates the pairwise distances between the elements in `Asplit{i}` and `Bsplit{i}`. You can view the code for pctdemo_task_hiv for full details.

job = createJob(myCluster); for i = 1:numTasks createTask(job, @pctdemo_task_hiv, 1, {Asplit{i}, Bsplit{i}, bf}); end

We can now submit the job and wait for it to finish.

submit(job); wait(job);

## Retrieve the Results

When we have obtained and verified all the results, we allow the cluster to free its resources. `fetchOutputs` will throw an error if the tasks did not complete successfully, in which case we need to delete the job before throwing the error.

try jobResults = fetchOutputs(job); catch err delete(job); rethrow(err); end pold = cell2mat(jobResults(:, 1))';

We have now finished all the verifications, so we can delete the job.

delete(job);

## Measure the Elapsed Time

The time used for the distributed computations should be compared against the time it takes to perform the same set of calculations in the Sequential Analysis of the Origin of the Human Immunodeficiency Virus example. The elapsed time varies with the underlying hardware and network infrastructure.

```
elapsedTime = etime(clock, startTime);
fprintf('Elapsed time is %2.1f seconds\n', elapsedTime);
```

Elapsed time is 34.8 seconds

## Plot the Results

Now that we have all the distances, we can construct the phylogenetic trees for the POL proteins. You can view the code for pctdemo_plot_hiv for full details.

pctdemo_plot_hiv(fig, pold, description);