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The cluster.split command can be used to assign sequences to OTUs and outputs a .list file. It splits large distance matrices into smaller peices ...
- Nearest neighbor: Each of the sequences within an OTU are at most X% distant from the most similar sequence in the OTU.
- Furthest neighbor: All of the sequences within an OTU are at most X% distant from all of the other sequences within the OTU.
- Average neighbor: This method is a middle ground between the other two algorithms.
- Opti: OTUs are assembled using metrics to determine the quality of clustering.
If there is an algorithm that you would like to see implemented, please consider either contributing to the mothur project or contacting the developers and we'll see what we can do. The opticlust algorithm is the default option. For this tutorial you should download the Final.zip file and decompress it.
- 1 Splitting your files
- 2 Clustering
- 3 Clustering with Vsearch
- 4 Finer points
- 5 Revisions
There are two part to the cluster.split command the splitting of your files into distinct groupings and the clustering of these groupings.
Splitting your files
The cluster.split command can split your files in 3 ways. Splitting by distance file, by classification, or by classification also using a fasta file. The splitmethod parameter allows you to specify how you want to split your files before you cluster, default=distance, options distance, classify or fasta.
Splitting by distance
For the distance file method, you need only provide your distance file and mothur will split the file into distinct groups.
mothur > cluster.split(phylip=final.phylip.dist)
mothur > cluster.split(column=final.dist, name=final.names)
The large parameter allows you to indicate that your distance matrix is too large to fit in RAM. The default value is false.
mothur > cluster.split(phylip=final.phylip.dist, large=T)
Splitting by classification
For the classification method, you need to provide your distance file and taxonomy file, and set the splitmethod to classify. You will also need to set the taxlevel you want to split by. mothur will split the sequences into distinct taxonomy groups, and split the distance file based on those groups.
mothur > cluster.split(column=final.dist, name=final.names, taxonomy=final.taxonomy, splitmethod=classify)
Splitting by classification using fasta
For the classification method using a fasta file, you need to provide your fasta file, names file and taxonomy file. You will also need to set the taxlevel you want to split by. mothur will split the sequence into distinct taxonomy groups, and create distance files for each grouping.
First you need to classify your sequences using the classify.seqs command.
mothur > cluster.split(fasta=final.fasta, name=final.names, taxonomy=final.taxonomy, splitmethod=fasta)
The taxonomy parameter allows you to enter the taxonomy file for your sequences, this is only valid if you are using splitmethod=classify or fasta.
The taxlevel parameter allows you to specify the taxonomy level you want to use to split the distance file, default=3, meaning use the third taxon in each list.
mothur > cluster.split(fasta=final.fasta, name=final.names, taxonomy=final.taxonomy, taxlevel=4)
The cluster parameter allows you to indicate whether you want to run the clustering or just split the distance matrix, default=T. The cluster=f option is used with the file option, see below.
mothur > cluster.split(fasta=final.fasta, name=final.names, taxonomy=final.taxonomy, splitmethod=fasta, taxlevel=4, cluster=f)
The file option which allows you to enter your file containing your list of column and names/count files as well as the singleton file. This file is mothur generated, when you run cluster.split() with the cluster=f parameter, see above. This can be helpful when you have a large dataset that you may be able to use all your processors for the splitting step, but have to reduce them for the cluster step due to RAM constraints. For example:
cluster.split(fasta=final.fasta, name=final.names, taxonomy=final.taxonomy, taxlevel=4, cluster=f, processors=8) cluster.split(file=final.file, processors=4)
This allows your to maximize your processors during the splitting step. Also, if you are unsure if the cluster step will have RAM issue with multiple processors, you can avoid running the first part of the command multiple times.
A names file contains two columns. The first column contains the name of a reference sequence that is in a distance matrix and the second column contains the names of the sequences (separated by commas) that the reference sequence represents. The list of names in the second column should always contain at least the reference sequence name.
There are several reasons to be interested in providing a name file with your distance matrix. First, as sequencing collections increase in size, the number of duplicate sequences is increasing. This is especially the case with sequences generated via pyrosequencing. Sogin and colleagues  found that less than 50% of their sequences were unique. Because the alignments and distances for the duplicate sequences are the same, re-processing each duplicate sequence takes a considerable amount of computing time and memory.
Example from final.names:
... GQY1XT001EYE6M GQY1XT001EYE6M,GQY1XT001D69D7,GQY1XT001A1LWJ GQY1XT001EXZXC GQY1XT001EXZXC GQY1XT001EXZLY GQY1XT001EXZLY GQY1XT001EXOOM GQY1XT001EXOOM GQY1XT001EX24Z GQY1XT001EX24Z,GQY1XT001AMCGM GQY1XT001EWUBU GQY1XT001EWUBU,GQY1XT001DJLCH,GQY1XT001B50B7 GQY1XT001EWJBM GQY1XT001EWJBM ...
Second, if you pre-screen a clone library using ARDRA then you may only have a sequence for a handful of clones, but you know the number of times that you have seen a sequence like it. In such a case the second column of the names file would contain the sequence name as well as dummy sequence names
... AA1234 AA1234,AA1234.1,AA1234.2 AA1235 AA1235 AA1236 AA1236,AA1236.1 AA1237 AA1237,AA1237.1,AA1237.2,AA1237.3 AA1238 AA1238,AA1238.1 ...
A count or name file is not required (unless you are using the column= option), but depending on the data set to be analyzed, could significantly accelerate the processing time of downstream calculations. In this simple example, the final dataset contains 51474 sequences. The distance matrix in the file final.phylip.dist is a lower triangle matrix for the 3772 unique sequences. While you could just read the matrix in and analyze the set of 3772 unqiue sequences, this would give a considerably different analysis than if you used the entire 51474 sequence data set. Considering the frequency of sequences is critical for pretty much every analysis in mothur, we want to use the name or count file to artificially inflate the matrix to its full size. In this case we use the namefile option:
mothur > cluster.split(phylip=final.phylip.dist, name=final.names)
mothur remembers that the distances for the reference sequence also apply to all of the sequences listed in the second column. Using a name file can considerably accelerate the amount of processing time required to analyze some data sets.
By default cluster.split() executes the opticlust clustering algorithm. For a detailed description of this and the other algorithms check out the example clustering calculations page.
The count file is similar to the name file in that it is used to represent the number of duplicate sequences for a given representative sequence. Mothur will use this information to form the correct OTU's. Unlike, when you use a names file the list file generated will contain only the unique names, so be sure to include the count file in downstream analysis with the list file.
mothur > make.table(name=final.names) Example from final.count_table: Representative_Sequence total GQY1XT001CFHYQ 467 GQY1XT001C44N8 3677 GQY1XT001C296C 4652 GQY1XT001ARCB1 2202 GQY1XT001CFWVZ 1967 GQY1XT001DHF2X 2137 GQY1XT001AEGCJ 2140 GQY1XT001CPCVN 2837 ... mothur > cluster.split(phylip=final.phylip.dist, count=final.count_table, taxonomy=final.taxonomy, taxlevel=4) label cutoff tp tn fp fn sensitivity specificity ppv npv fdr accuracy mcc f1score 0.03 0.03 31138 7044624 7501 21302 0.5938 0.9989 0.8059 0.997 0.1941 0.9959 0.6898 0.6838
The methods available in mothur include opticlust (opti), average neighbor (average), furthest neighbor (furthest), nearest neighbor (nearest), Vsearch agc (agc), Vsearch dgc (dgc). By default cluster() uses the opticlust algorithm; this can be changed with the method option.
mothur > cluster.split(fasta=final.fasta, count=final.count_table, taxonomy=final.taxonomy, taxlevel=4, method=opti)
To obtain a average neighbor clustering of the data use the method option to produce the subsequent output:
mothur > cluster.split(fasta=final.fasta, count=final.count_table, taxonomy=final.taxonomy, taxlevel=4, method=average, cutoff=0.15)
The metric parameter allows to select the metric in the opticluster method. Options are Matthews correlation coefficient (mcc), sensitivity (sens), specificity (spec), true positives + true negatives (tptn), false positives + false negatives (fpfn), true positives (tp), true negative (tn), false positive (fp), false negative (fn), f1score (f1score), accuracy (accuracy), positive predictive value (ppv), negative predictive value (npv), false discovery rate (fdr). Default=mcc.
mothur > cluster.split(fasta=final.fasta, count=final.count_table, taxonomy=final.taxonomy, taxlevel=4, metric=tptn) abel cutoff tp tn fp fn sensitivity specificity ppv npv fdr accuracy mcc f1score 0.03 0.03 28828 7054934 4826 23518 0.5507 0.9993 0.8566 0.9967 0.1434 0.996 0.6851 0.6704
The initialize parameter allows to select the initial randomization for the opticluster method. Options are singleton, meaning each sequence is randomly assigned to its own OTU, or oneotu meaning all sequences are assigned to one otu. We have found initialize=singleton to produce better clustering in less time. Default=singleton.
The delta parameter allows to set the stable value for the metric in the opticluster method Default delta=0.0001. To reach a full convergence, set delta=0.
The iters parameter allow you to set the maxiters for the opticluster method. Default=100.
With the opticlust method the list file is created for the cutoff you set. The default cutoff is 0.03. With the average neighbor, furthest neighbor and nearest neighbor methods the cutoff should be significantly higher than the desired distance in the list file. We suggest cutoff=0.20. This will provide a boost in speed and less RAM will be required than if you didn't set the cutoff for reading in the matrix. The cutoff can be set for the cluster command as follows:
mothur > cluster.split(fasta=final.fasta, count=final.count_table, taxonomy=final.taxonomy, taxlevel=4, cutoff=0.05) label cutoff tp tn fp fn sensitivity specificity ppv npv fdr accuracy mcc f1score 0.05 0.05 133482 6888777 30337 59510 0.6916 0.9956 0.8148 0.9914 0.1852 0.9874 0.7444 0.7482
If you want greater precision, there is a precision option in the cluster() command:
mothur > cluster.split(column=final.dist, count=final.count_table, method=average, precision=1000, cutoff=0.10)
The final.an.unique_list.list file will look like:
unique 3772 GQY1XT001C296C GQY1XT001C44N8 GQY1XT001DC1IC ... 0.004 3772 GQY1XT001C296C GQY1XT001C44N8 GQY1XT001DC1IC... 0.005 3317 GQY1XT001C296C,GQY1XT001B9EHX GQY1XT001C44N8... 0.006 3259 GQY1XT001C296C,GQY1XT001B9EHX GQY1XT001C44N8... ...
Remember that the 16S rRNA gene is roughly 1,500 bp long. So it would seem silly to have a precision greater than 1,000. Just because you can calculate a number to 20 digits, doesn't mean they're all significant.
The runsensspec parameter allows to run the sens.spec command on the completed list file. Default=true.
Default processors=Autodetect number of available processors and use all available. You can set processors to 2 with the following option:
mothur> cluster.split(fasta=final.fasta, count=final.count_table, taxonomy=final.taxonomy, taxlevel=4, processors=2)
Clustering with Vsearch
The vsearch program is written by the vsearch team. You can now use vsearch clustering methods through mothur.
Vsearch requires a fasta file to cluster.
mothur > cluster.split(fasta=final.fasta, count=final.count_table, taxonomy=final.taxonomy, method=agc)
The available clustering methods are agc and dgc.
mothur > cluster(fasta=final.fasta, count=final.count_table, taxonomy=final.taxonomy, method=dgc)
Perhaps the second most commonly asked question is why there isn't a line for distance 0.XX. If you notice the previous example the distances jump from 0.003 to 0.006. Where are 0.004 and 0.005? mothur only outputs data if the clustering has been updated for a distance. So if you don't have data at your favorite distance, that means that nothing changed between the previous distance and the next one. Therefore if you want OTU data for a distance of 0.005 in this case, you would use the data from 0.003.
You may notice that if you run the same command multiple times for the same dataset you might get slightly different out for some distances:
mothur > cluster.split(column=final.dist, count=final.count_table) label cutoff tp tn fp fn sensitivity specificity ppv npv fdr accuracy mcc f1score 0.03 0.03 30772 7052222 7538 21574 0.5879 0.9989 0.8032 0.997 0.1968 0.9959 0.6852 0.6789
mothur > cluster.split(column=final.dist, count=final.count_table) label cutoff tp tn fp fn sensitivity specificity ppv npv fdr accuracy mcc f1score 0.03 0.03 31313 7051732 8028 21033 0.5982 0.9989 0.7959 0.997 0.2041 0.9959 0.6881 0.683
The variability is caused by the randomization of the sequences.
- 1.27.0 - reduced memory by 50% and increased speed by 55%.
- 1.28.0 - added count parameter
- 1.29.0 - added cluster parameter
- 1.30.0 - no longer creates concatenated distance matrix for splitmethod=fasta.
- 1.31.0 - Bug Fix: - when splitting by taxonomy mothur was saving temp fasta files as the "current" fasta file.
- 1.34.0 - added the file option which allows you to enter your file containing your list of column and names/count files as well as the singleton file. This file is mothur generated, when you run cluster.split() with the cluster=f parameter. This can be helpful when you have a large dataset that you may be able to use all your processors for the splitting step, but have to reduce them for the cluster step due to RAM constraints. For example: cluster.split(fasta=yourFasta, taxonomy=yourTax, count=yourCount, taxlevel=3, cluster=f, processors=8) then cluster.split(file=yourFile, processors=4). This allows your to maximize your processors during the splitting step. Also, if you are unsure if the cluster step will have RAM issue with multiple processors, you can avoid running the first part of the command multiple times.
- 1.35.0 - Clustering commands did not include the count file info. when printing list file OTU order. Only effects clustering commands. *.pick commands must preserve otuLabels order. - http://www.mothur.org/forum/viewtopic.php?f=3&t=3460&p=10483#p10483
- 1.35.0 - Bug Fix: MPI version compile issue, http://www.mothur.org/forum/viewtopic.php?f=4&t=3453&p=10073#p10073. fixed in 1.34.1.
- 1.36.0 - Bug Fix: did not allow you to use the classic option with the file option.
- 1.37.0 - Adds vsearch clustering methods: agc and dgc. #169
- 1.37.0 - Bug Fix: Removes OS limit on open files. #142
- 1.38.0 - Fixes bug with age method.
- 1.38.1 - Removes hard parameter.
- 1.39.0 - Adds opticlust method. opti new default clustering method.
- 1.39.0 - Adds agc and dgc methods of Windows users.
- 1.39.1 - Corrects printing issues with opticlust method.
- 1.39.1 - Adds runsensspec parameter
- 1.40.0 - Allow for () characters in taxonomy definitions. #350
- 1.40.0 - Rewrite of threaded code. Default processors=Autodetect number of available processors and use all available.
- 1.40.4 - Bug Fix: Cluster commands printing of list file. #454
- 1.43.0 - Changes datatype for opti method to correct overflow.