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Releases: gbouras13/pypolca

0.3.1

02 Feb 06:11
54eaa2b
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  • Adds --careful to log file to make it clear if it has been run

v0.3.0

17 Jan 09:05
56a7642
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  • Includes a number of changes by @rrwick
  • Fixes errors with counts in the report
  • Fixes issue where pypolca would crash if there were spaces in the FASTA header
  • Adds --min_alt, --min_ratio and --careful parameters
  • Using --careful is recommended for low read depth (<25x coverage)

v0.2.1

19 Dec 03:09
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  • Fixes bug in generating the report. If there were multiple alleles at a certain site (on a certain line in the vcf), this would crash pypolca. Exception handling has been added.
  • Thanks @oschwengers and @npbhavya for detecting this

v0.2.0

05 Nov 22:53
b1d77e8
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  • Fixes bug where pypolca would warn it found 0 variants when in fact there were variants.
  • Also would result in the polishing not working.
  • Please upgrade if you have used v0.1.1!
  • Importantly, this release adds benchmarking of pypolca v0.2.0 vs POLCA more thoroughly.

v0.1.1

09 Oct 02:50
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  • Patch release to fix the release.yaml uploads to pypi.
  • Also adds DOI with Zenodo

v0.1.0 9 October 2023

09 Oct 02:19
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  • Initial release
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
  -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]