This program reads one or more input FASTA files. For each file it computes a variety of statistics, and then prints a summary of the statistics as output.
In the examples below, $ indicates the command line prompt.
This program is released as open source software under the terms of MIT License.
You can install bionitio directly from the source code or build and run it from within Docker container.
Clone this repository:
$ git clone https://github.com/bionitio-team/bionitio-haskell
Move into the repository directory:
$ cd bionitio-haskell
We recommend using the stack tool to install bionitio. You will need to install stack on your system first.
On OS X this can be can with homebrew like so (you may need to run brew update first):
% brew install stack
Once you have stack installed you can use it to build bionitio like so:
% stack install
The file Dockerfile contains instructions for building a Docker container for bionitio.
If you have Docker installed on your computer you can build the container like so:
$ docker build -t bionitio .
See below for information about running bionitio within the Docker container.
Bionitio accepts zero or more FASTA filenames on the command line. If zero filenames are specified it reads a single FASTA file from the standard input device (stdin). Otherwise it reads each named FASTA file in the order specified on the command line. Bionitio reads each input FASTA file, computes various statistics about the contents of the file, and then displays a tab-delimited summary of the statistics as output. Each input file produces at most one output line of statistics. Each line of output is prefixed by the input filename or by the text "stdin" if the standard input device was used.
Bionitio processes each FASTA file one sequence at a time. Therefore the memory usage is proportional to the longest sequence in the file.
An optional command line argument --minlen can be supplied. Sequences with length strictly less than the given value will be ignored by bionitio and do not contribute to the computed statistics. By default --minlen is set to zero.
These are the statistics computed by bionitio, for all sequences with length greater-than-or-equal-to --minlen:
- NUMSEQ: the number of sequences in the file satisfying the minimum length requirement.
- TOTAL: the total length of all the counted sequences.
- MIN: the minimum length of the counted sequences.
- AVERAGE: the average length of the counted sequences rounded down to an integer.
- MAX: the maximum length of the counted sequences.
If there are zero sequences counted in a file, the values of MIN, AVERAGE and MAX cannot be computed. In that case bionitio will print a dash (-) in the place of the numerical value. Note that when --minlen is set to a value greater than zero it is possible that an input FASTA file does not contain any sequences with length greater-than-or-equal-to the specified value. If this situation arises bionitio acts in the same way as if there are no sequences in the file.
Bionitio can display usage information on the command line via the -h or --help argument:
% bionitio -h
Usage: bionitio [--minlen N] [--version] [--verbose] [[FASTA_FILE ...]]
Print fasta stats
Available options:
-h,--help Show this help text
--minlen N Minimum length sequence to include in stats
(default=0)
--version Print version and exit
--verbose Print more stuff about what's happening
Bionitio accepts zero or more named FASTA files on the command line. These must be specified following all other command line arguments. If zero files are named, bionitio will read a single FASTA file from the standard input device (stdin).
There are no restrictions on the name of the FASTA files. Often FASTA filenames end in .fa or .fasta, but that is merely a convention, which is not enforced by bionitio.
The example below illustrates bionitio applied to a single named FASTA file called file1.fa:
$ bionitio file1.fa
FILENAME NUMSEQ TOTAL MIN AVG MAX
file1.fa 5264 3801855 31 722 53540
The example below illustrates bionitio applied to three FASTA files called file1.fa, file2.fa and file3.fa:
$ bionitio file1.fa file2.fa file3.fa
FILENAME NUMSEQ TOTAL MIN AVG MAX
file1.fa 5264 3801855 31 722 53540
file2.fa 1245 982374 8 393 928402
file3.fa 64 8376 102 123 212
The example below illustrates bionitio reading a FASTA file from standard input. In this example we have redirected the contents of a file called file1.fa into the standard input using the shell redirection operator <:
$ bionitio < file1.fa
FILENAME NUMSEQ TOTAL MIN AVG MAX
stdin 5264 3801855 31 722 53540
Equivalently, you could achieve the same result by piping a FASTA file into bionitio:
$ cat file1.fa | bionitio
FILENAME NUMSEQ TOTAL MIN AVG MAX
stdin 5264 3801855 31 722 53540
Bionitio provides an optional command line argument --minlen which causes it to ignore (not count) any sequences in the input FASTA files with length strictly less than the supplied value.
The example below illustrates bionitio applied to a single FASTA file called file.fawith a--minlen` filter of 1000.
$ bionitio --minlen 1000 file.fa
FILENAME NUMSEQ TOTAL MIN AVG MAX
file1.fa 4711 2801855 1021 929 53540
If the --log FILE command line argument is specified, bionitio will output a log file containing information about program progress. The log file includes the command line used to execute the program, and a note indicating which files have been processes so far. Events in the log file are annotated with their date and time of occurrence.
$ bionitio --log bt.log file1.fasta file2.fasta
It is possible that the input FASTA file contains zero sequences, or, when the --minlen command line argument is used, it is possible that the file contains no sequences of length greater-than-or-equal-to the supplied value. In both of those cases bionitio will not be able to compute minimum, maximum or average sequence lengths, and instead it shows output in the following way:
The example below illustrates bionitio applied to a single FASTA file called empty.fa which contains zero sequences:
$ bionitio empty.fa
FILENAME NUMSEQ TOTAL MIN AVG MAX
empty.fa 0 0 - - -
Bionitio returns the following exit status values:
- 0: The program completed successfully.
- 1: File I/O error. This can occur if at least one of the input FASTA files cannot be opened for reading. This can occur because the file does not exist at the specified path, or bionitio does not have permission to read from the file.
- 2: A command line error occurred. This can happen if the user specifies an incorrect command line argument. In this circumstance bionitio will also print a usage message to the standard error device (stderr).
The following section describes how to run bionitio within the Docker container. It assumes you have Docker installed on your computer and have built the container as described above. The container behaves in the same way as the normal version of bionitio, however there are some Docker-specific details that you must be aware of.
The general syntax for running bionitio within Docker is as follows:
$ docker run -i bionitio CMD
where CMD should be replaced by the specific command line invocation of bionitio. Specific examples are below.
Display the help message:
$ docker run -i bionitio bionitio -h
Note: it may seem strange that bionitio is mentioned twice in the command. The first instance is the name of the Docker container and the second instance is the name of the bionitio executable that you want to run inside the container.
Display the version number:
$ docker run -i bionitio bionitio --version
Read from a single input FASTA file redirected from standard input:
$ docker run -i bionitio bionitio < file.FASTA
Read from multuple input FASTA files named on the command line, where all the files are in the same directory. You must replace DATA with the absolute file path of the directory containing the FASTA files:
$ docker run -i -v DATA:/in bionitio bionitio /in/file1.fasta /in/file2.fasta /in/file3.fasta
The argument DATA:/in maps the directory called DATA on your local machine into the /in directory within the Docker container.
Logging progress to a file in the directory OUT:
$ docker run -i -v DATA:/in -v OUT:/out bionitio-c bionitio --log /out/logfile.txt /in/file1.fasta /in/file2.fasta /in/file3.fasta
Replace OUT with the absolute path of the directory to write the log file. For example, if you want the log file written to the current working directory, replace OUT with $PWD.
As above, you will also need to replace DATA with the absolite path to the directory containing your input FASTA files.
You can run the unit tests for bionitio with the following commands:
% cd bionitio/haskell
% runhaskell -isrc -itest test/Test.hs
Sample test input files are provided in the functional_tests/test_data folder.
$ cd functional_tests/test_data
$ bionitio two_sequence.fasta
FILENAME TOTAL NUMSEQ MIN AVG MAX
two_sequence.fasta 2 357 120 178 237
Automated tests can be run using the functional_tests/bionitio-test.sh script like so:
$ cd functional_tests
$ ./bionitio-test.sh -p bionitio -d test_data
The -p argument specifies the name of the program to test, the -d argument specifies the path of the directory containing test data.
The script will print the number of passed and failed test cases. More detailed information about each test case can be obtained
by requesting "verbose" output with the -d flag:
$ ./bionitio-test.sh -p bionitio -d test_data -v
The test script can also be run inside the Docker container:
$ docker run bionitio /bionitio/functional_tests/bionitio-test.sh -p bionitio -d /bionitio/functional_tests/test_data -v
The Common Workflow Language (CWL) specifies a portable mechanism for running software tools and workflows across many different platforms.
We provide an example CWL wrapper for bionitio in the file bionitio.cwl. It invokes bionitio using the Docker container (described above). This wrapper allows you
to easily incorporate bionitio into CWL workflows, and can be executed by any CWL-supporting workflow engine.
You can test the wrapper using the cwltool workflow runner, which is provided by the CWL project (see the CWL documentation for how to install this on your computer).
$ cwltool bionitio.cwl --fasta_file file.fasta
Please submit bug reports and feature requests to the issue tracker on GitHub: