pypolca
is a Standalone Python re-implementation of the POLCA polisher from the MaSuRCA genome assembly and analysis toolkit.
pypolca
also adds a --careful
flag that we have shown is (generally) the best performing short-read bacterial isolate genome polishing option across a range of depths and samples.
The ‑‑careful
flag requires at least 4 reads to support the alternative allele, and a minimum ratio of 3 (i.e. at least three times as many reads must support the alterative allele compared to the reference allele). This prevents almost all false positives at low depths without sacrificing error removal sensitivity.
Therefore, we recommend you always use pypolca
with --careful
For more information about pypolca
and pypolca --careful
, along with Polypolish's new --careful
option and our analysis of short-read polishing methods for near-perfect Nanopore assemblies, please read our manuscript introducing pypolca
:
Bouras G, Judd LM, Edwards RA, Vreugde S, Stinear TP, Wick RR. How low can you go? Short-read polishing of Oxford Nanopore bacterial genome assemblies. Microbial Genomics. 2024. doi: https://doi.org/10.1099/mgen.0.001254.
# creates conda environment with pypolca
conda create -n pypolca_env pypolca
# activates conda environment
conda activate pypolca_env
# runs pypolca with --careful
pypolca run -a <genome> -1 <R1 short reads file> -2 <R2 short reads file> -t <threads> -o <output directory> --careful
pypolca
is a python reimplenetation of the POLCA polisher from the MaSuRCA genome assembly and analysis toolkit that was made for inclusion into the hybrid bacterial genome assembly tool hybracter.
It was written for a number of reasons:
- MaSuRCA is only available on Linux, not for MacOS.
- The original
polca.sh
script from MaSuRCA was difficult to use because you could not specify an output directory. Additionally, due to its shell implementation, both FASTQ read files needed to be input together as a string - To use
polca.sh
, you need to install the entire MaSuRCA assembly toolkit. - POLCA is recommended for long-read first bacterial assembly polishing (see this paper) and I wanted to include it for MacOS and Linux in hybracter.
Note: I neither guarantee nor desire that pypolca
will give identical results to POLCA implemented in MaSuRCA. This is because of the different versions of freebayes and Samtools that might be used as a dependency.
In testing, pypolca
v0.2.0 (running Freebayes v1.3.6 and Samtools v1.18) was extremely similar, but not identical to POLCA (running Freebayes v1.3.1-dirty and Samtools v0.1.20). Please see benchmarking for more details.
I have decided to use the newest versions of freebayes and Samtools possible rather than the version installed with MaSuRCA, for ease of maintenance and particularly because the version of Samtools used is a major version behind and the CLI has changed.
- I have implemeted
pypolca
predominantly for the use-case of polishing long-read bacterial genome assemblies with short reads. Therefore, I decided not to implement the batched multiprocessing of freebayes included in POLCA, because it was a lot of work for no benefit for most bacterial genomes. - However, this is certainly not true for larger genomes such as eukaryotic organisms.
pypolca
should be a lot slower than POLCA for such organisms if you run both with more than 1 thread. - I do not intend to implement multiprocessing but if someone wants to feel free to make a PR.
Installation from conda is recommended as this will install all non-python dependencies.
pypolca
is available on bioconda.
conda install -c bioconda pypolca
You can also install the Python components of pypolca
with pip.
pip install pypolca
Alternatively, the development version of pypolca
can be installed manually via github.
git clone https://github.com/gbouras13/pypolca.git
cd pypolca
pip install -e .
pypolca -h
If you have install pypolca
with pip or from source, you will then need to install the external dependencies separately, which can be found in build/environment.yaml
Usage: pypolca [OPTIONS] COMMAND [ARGS]...
Options:
-h, --help Show this message and exit.
-V, --version Show the version and exit.
Commands:
citation Print the citations for polca
run Python implementation of the POLCA polisher from MaSuRCA
Usage: pypolca run [OPTIONS]
Python implementation of the POLCA polisher from MaSuRCA
Options:
-h, --help Show this message and exit.
-V, --version Show the version and exit.
-a, --assembly PATH Path to assembly contigs or scaffolds. [required]
-1, --reads1 PATH Path to polishing reads R1 FASTQ. Can be FASTQ or
FASTQ gzipped. Required. [required]
-2, --reads2 PATH Path to polishing reads R2 FASTQ. Can be FASTQ or
FASTQ gzipped. Optional. Only use -1 if you have
single end reads.
-t, --threads INTEGER Number of threads. [default: 1]
-o, --output PATH Output directory path [default: output_polca]
-f, --force Force overwrites the output directory
--min_alt INTEGER Minimum alt allele count to make a change
[default: 2]
--min_ratio FLOAT Minimum alt allele to ref allele ratio to make a
change [default: 2.0]
--careful Equivalent to --min_alt 4 --min_ratio 3
-n, --no_polish do not polish, just create vcf file, evaluate the
assembly and exit
-m, --memory_limit TEXT Memory per thread to use in samtools sort, set to
2G or more for large genomes [default: 2G]
-p, --prefix TEXT prefix for output files [default: polca]
The polished output FASTA will be {prefix}_corrected.fasta
in the specified output directory and the POLCA report will be the textfile {prefix}.report
Please cite pypolca
in your paper using both:
Bouras G, Judd LM, Edwards RA, Vreugde S, Stinear TP, Wick RR. How low can you go? Short-read polishing of Oxford Nanopore bacterial genome assemblies. Microbial Genomics. 2024. doi: https://doi.org/10.1099/mgen.0.001254.
Zimin AV, Salzberg SL (2020) The genome polishing tool POLCA makes fast and accurate corrections in genome assemblies. PLoS Comput Biol 16(6): e1007981. https://doi.org/10.1371/journal.pcbi.1007981.