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πŸπŸŸ‘β™¦οΈπŸŸ¦ PyHMMER Stars

Cython bindings and Python interface to HMMER3.

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πŸ—ΊοΈ Overview

HMMER is a biological sequence analysis tool that uses profile hidden Markov models to search for sequence homologs. HMMER3 is developed and maintained by the Eddy/Rivas Laboratory at Harvard University.

pyhmmer is a Python package, implemented using the Cython language, that provides bindings to HMMER3. It directly interacts with the HMMER internals, which has the following advantages over CLI wrappers (like hmmer-py):

This library is still a work-in-progress, and in an experimental stage, but it should already pack enough features to run biological analyses or workflows involving hmmsearch, hmmscan, nhmmer, phmmer, hmmbuild and hmmalign.

πŸ”§ Installing

pyhmmer can be installed from PyPI, which hosts some pre-built CPython wheels for Linux and MacOS on x86-64 and Arm64, as well as the code required to compile from source with Cython:

$ pip install pyhmmer

Compilation for UNIX PowerPC is not tested in CI, but should work out of the box. Note than non-UNIX operating systems (such as Windows) are not supported by HMMER.

A Bioconda package is also available:

$ conda install -c bioconda pyhmmer

πŸ”– Citation

PyHMMER is scientific software, with a published paper in the Bioinformatics. Please cite both PyHMMER and HMMER if you are using it in an academic work, for instance as:

PyHMMER (Larralde et al., 2023), a Python library binding to HMMER (Eddy, 2011).

Detailed references are available on the Publications page of the online documentation.

πŸ“– Documentation

A complete API reference can be found in the online documentation, or directly from the command line using pydoc:

$ pydoc pyhmmer.easel
$ pydoc pyhmmer.plan7

πŸ’‘ Example

Use pyhmmer to run hmmsearch to search for Type 2 PKS domains (t2pks.hmm) inside proteins extracted from the genome of Anaerococcus provencensis (938293.PRJEB85.HG003687.faa). This will produce an iterable over TopHits that can be used for further sorting/querying in Python. Processing happens in parallel using Python threads, and a TopHits object is yielded for every HMM passed in the input iterable.

import pyhmmer

with pyhmmer.easel.SequenceFile("pyhmmer/tests/data/seqs/938293.PRJEB85.HG003687.faa", digital=True) as seq_file:
    sequences = list(seq_file)

with pyhmmer.plan7.HMMFile("pyhmmer/tests/data/hmms/txt/t2pks.hmm") as hmm_file:
    for hits in pyhmmer.hmmsearch(hmm_file, sequences, cpus=4):
      print(f"HMM {hits.query_name.decode()} found {len(hits)} hits in the target sequences")

Have a look at more in-depth examples such as building a HMM from an alignment, analysing the active site of a hit, or fetching marker genes from a genome in the Examples page of the online documentation.

πŸ’­ Feedback

⚠️ Issue Tracker

Found a bug ? Have an enhancement request ? Head over to the GitHub issue tracker if you need to report or ask something. If you are filing in on a bug, please include as much information as you can about the issue, and try to recreate the same bug in a simple, easily reproducible situation.

πŸ—οΈ Contributing

Contributions are more than welcome! See CONTRIBUTING.md for more details.

⏱️ Benchmarks

Benchmarks were run on a i7-10710U CPU running @1.10GHz with 6 physical / 12 logical cores, using a FASTA file containing 4,489 protein sequences extracted from the genome of Escherichia coli (562.PRJEB4685) and the version 33.1 of the Pfam HMM library containing 18,259 domains. Commands were run 3 times on a warm SSD. Plain lines show the times for pressed HMMs, and dashed-lines the times for HMMs in text format.

Benchmarks

Raw numbers can be found in the benches folder. They suggest that phmmer should be run with the number of logical cores, while hmmsearch should be run with the number of physical cores (or less). A possible explanation for this observation would be that HMMER platform-specific code requires too many SIMD registers per thread to benefit from simultaneous multi-threading.

To read more about how PyHMMER achieves better parallelism than HMMER for many-to-many searches, have a look at the Performance page of the documentation.

πŸ” See Also

Building a HMM from scratch? Then you may be interested in the pyfamsa package, providing bindings to FAMSA, a very fast multiple sequence aligner. In addition, you may want to trim alignments: in that case, consider pytrimal, which wraps trimAl 2.0.

If despite of all the advantages listed earlier, you would rather use HMMER through its CLI, this package will not be of great help. You can instead check the hmmer-py package developed by Danilo Horta at the EMBL-EBI.

βš–οΈ License

This library is provided under the MIT License. The HMMER3 and Easel code is available under the BSD 3-clause license. See vendor/hmmer/LICENSE and vendor/easel/LICENSE for more information.

This project is in no way affiliated, sponsored, or otherwise endorsed by the original HMMER authors. It was developed by Martin Larralde during his PhD project at the European Molecular Biology Laboratory in the Zeller team.