Support is provided at the forums, by email or the GitHub issues page. For support requests it is usually helpful if you provide details about your data (size and type of sequences) and your execution environment (CPU cores, RAM, operating system).
Community feedback and feature requests are also appreciated.
How to run the program on multiple input files?
It is not recommended to run more than one instance of DIAMOND simultaneously on the same machine, because it is more efficient if you allocate more ressources to a single task by increasing the block size parameter
-b and using lower numbers for
-c. For this reason, input files should be processed consecutively. Pipes can also be used process multiple input files. For example, this command will build a database from all
fasta.gz files in the current directory:
zcat *.fasta.gz | diamond makedb -d diamond_db
The program runs for a very long time and the output file remains empty.
This is normal. Larger databases are split into chunks and the output is kept in temporary files at first and only merged in the end.
There are no temporary files.
The temporary files are not visible using standard shell commands because
unlink is invoked on them after creation, which ensures that the files will be removed in case of ungraceful termination of the program.
More than one alignment is reported for a single query and subject sequence.
Due to the definition of HSPs, which are pairs of segments that form a linear alignment, any number of these may be contained in a single query/subject pair. The program reports additional aligned domains by default as they may contain valuable information. This behaviour can be changed by using the
The program does not appear to be sensitive enough / it does not find an alignment I expect it to find or that another aligner reported.
There are a number of reasons that can cause hits to not be found or reported. In particular, even identical self-alignments of protein sequences may not be reported for some of the reasons listed below.
The hit may not be deemed significant, i.e. its e-value is above the configured cutoff. This is possible even for short 100% identity matches. Also note that e-value computations are not compatible for different aligners most of the time.
Low complexity masking and compositional bias correction may cause hits to be filtered. This is usually desirable as these methods are highly effective in eliminating false positives. Note that differences in false positive filtering can cause substantial deviations in the output for different aligners used on the same data.
Due to its seed configuration, the program is not able to align sequences shorter than 12 or 10 amino acids, for the fast mode and sensitive modes respectively.
Seeds that occur too frequently in the input are ignored, which may cause problems if your data is extremely repetitive. This behaviour can be adjusted using the
The program may not be sensitive enough for your application. You should try the more sensitive modes (options
--more-sensitive). Still, perfect results cannot be guaranteed by heuristical algorithms, but only by a rigorous Smith-Waterman computation.
The program terminates with an unclear or no error message.
The task may have been killed by the system for running out of memory. Use
dmesg to check for a respective kernel message. See instructions on memory usage. If you run the program on a cluster, you may need to allocate more memory to the task.
Are results consistent for multiple calls of the program?
The program has a basic consistency guarantee that the same version run on the same input with the same parameters will produce identical results, regardless of the hardware, operating system, compiler, or number of CPU threads. If this was not the case, I would consider it a bug.
Beyond that, no guarantees of consistency can be made. DIAMOND like all fast aligners uses numerous heuristics that can alter results in unexpected ways.