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Merge pull request #16 from cokelaer/main
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switch working directory back to fastq/
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cokelaer committed Dec 6, 2023
2 parents 666f61e + 014ed35 commit 47da7fa
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33 changes: 33 additions & 0 deletions .pre-commit-config.yaml
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files: '\.(py|rst|sh)$'
fail_fast: false

repos:
- repo: https://github.com/pre-commit/pre-commit-hooks
rev: v3.2.0
hooks:
- id: trailing-whitespace
- id: end-of-file-fixer
- id: check-yaml
#- id: check-executables-have-shebangs
- id: check-ast

- repo: https://github.com/pycqa/flake8
rev: 6.1.0
hooks:
- id: flake8
args: ["-j8", "--ignore=E203,E501,W503,E722", "--max-line-length=120", "--exit-zero"]

- repo: https://github.com/psf/black
rev: 22.10.0
hooks:
- id: black
args: ["--line-length=120"]
exclude: E501

- repo: https://github.com/pycqa/isort
rev: 5.12.0
hooks:
- id: isort
args: ["--profile", "black"] # solves conflicts between black and isort

42 changes: 21 additions & 21 deletions README.rst
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Expand Up @@ -99,14 +99,14 @@ Details
.. image:: https://raw.githubusercontent.com/sequana/demultiplex/master/sequana_pipelines/demultiplex/dag.png

This pipeline runs bcl2fastq 2.20 and creates a set of diagnostics plots to help
deciphering common issues such as missing index and sample sheet errors.
deciphering common issues such as missing index and sample sheet errors.


Rules and configuration details
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Here is the `latest documented configuration file <https://raw.githubusercontent.com/sequana/demultiplex/master/sequana_pipelines/demultiplex/config.yaml>`_
to be used with the pipeline. Each rule used in the pipeline may have a section in the configuration file.
to be used with the pipeline. Each rule used in the pipeline may have a section in the configuration file.



Expand All @@ -116,8 +116,9 @@ Changelog
========= =======================================================================
Version Description
========= =======================================================================
1.5.1 * swictch working directory to fastq instead of demultiplex(regression)
1.5.0 * Uses click and new sequana_pipetools, add multiqc
1.4.0 * Implement demultiplexing of single cell ATAC seq data with
1.4.0 * Implement demultiplexing of single cell ATAC seq data with
cellranger.
1.3.1 * use sequana_wrappers version in the config file
1.3.0 * use latest sequana-wrappers to benefit and graphivz apptainer
Expand All @@ -129,8 +130,8 @@ Version Description
1.1.0 * Uses new sequana-wrappers repository
1.0.5 * Fix regression bug to cope with new snakemake API
* Compatibility with sequanix GUI
1.0.4 * Better HTML report with updated images.
* validate the SampleSheet when using sequana_demultiplex and/or the
1.0.4 * Better HTML report with updated images.
* validate the SampleSheet when using sequana_demultiplex and/or the
pipeline
* Add error handler from sequana_pipetools
* save all undetermined barcodes (not just first 20)
Expand All @@ -139,7 +140,7 @@ Version Description
it can be used in Sequanix
1.0.3 * remove check_samplesheet and fix_samplesheet modules now in sequana
* check sample sheet but do not fail. Instead, informing users that
there is an error and suggest to use 'sequana samplesheet
there is an error and suggest to use 'sequana samplesheet
--quick-fix'
1.0.2 Use 'sequana samplesheet --check ' command instead of deprecated
sequana_check_sample_sheet command
Expand All @@ -152,40 +153,40 @@ Version Description
* The --ignore-missing-bcls option is changed into
--no-ignore-missing-bcls so as to ignore missing bcls by default
keep this option as a flag and keep same behaviour
* Fix HTML syntax
* Fix HTML syntax
1.0.0 * stable version pinned on sequana libraries
0.9.11 * fix label in plot_summary,
0.9.11 * fix label in plot_summary,
* add new plot to show reads per sample + undetermined
* add two tools one to check the samplesheet called
sequana_sample_sheet and one called sequana_fix_samplesheet. The
* add two tools one to check the samplesheet called
sequana_sample_sheet and one called sequana_fix_samplesheet. The
former is now inside the pipeline as well and when creating the
pipeline
* set --write_reverse_complement to False by default
* remove the --ignore-missing-control which is deprecated anyway
0.9.10 * implement the new option --from-project, add missing MANIFEST
0.9.9 * simplification of the pipeline to use sequana 0.8.4 to speed up
0.9.9 * simplification of the pipeline to use sequana 0.8.4 to speed up
the --help calls.
* include a summary HTML report
* include a summary HTML report
0.9.8 * fix typos
0.9.7 * Use new release of sequana_pipetools
* set matplotlib backend to agg
* include a simple HTML report
0.9.6 * Handle different RunParameter.xml name (NextSeq vs HiSeq)
0.9.5 * Fix a regression bug due to new sequana release. We do not check
0.9.5 * Fix a regression bug due to new sequana release. We do not check
the input file (fastq) since this is not a sequence analysis
pipeline
* Check whether it is a NextSeq run. If so, merging-strategy must be
set to 'merge'. Can be bypassed using --force
0.9.4 * Check the presence of the bcl input directory and samplesheet.
* More help in the --help message.
0.9.4 * Check the presence of the bcl input directory and samplesheet.
* More help in the --help message.
* add --sample-sheet option to replace --samplesheet option
* Fix the schema file
* Check for presence of RunParameters.xml and provide information
if merging-stratgy is set to None whereas it is a NextSeq run
0.9.3 Fix regression bug
0.9.2 remove warning due to relative paths.
0.9.1 Make the merging options compulsory. Users must tell whether they
want to merge the lanes or not. This avoid to do the merging or not
0.9.2 remove warning due to relative paths.
0.9.1 Make the merging options compulsory. Users must tell whether they
want to merge the lanes or not. This avoid to do the merging or not
whereas the inverse was expected.
0.8.6 Uses 64G/biomics queue and 16 cores on a SLURM scheduler
========= =======================================================================
Expand All @@ -195,7 +196,6 @@ Version Description
Contribute & Code of Conduct
~~~~~~~~~~~~~~~~~~~~~~~~~~~~

To contribute to this project, please take a look at the
`Contributing Guidelines <https://github.com/sequana/sequana/blob/master/CONTRIBUTING.rst>`_ first. Please note that this project is released with a
To contribute to this project, please take a look at the
`Contributing Guidelines <https://github.com/sequana/sequana/blob/master/CONTRIBUTING.rst>`_ first. Please note that this project is released with a
`Code of Conduct <https://github.com/sequana/sequana/blob/master/CONDUCT.md>`_. By contributing to this project, you agree to abide by its terms.

2 changes: 1 addition & 1 deletion pyproject.toml
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Expand Up @@ -4,7 +4,7 @@ build-backend = "poetry.core.masonry.api"

[tool.poetry]
name = "sequana-demultiplex"
version = "1.5.0"
version = "1.5.1"
description = "Pipeline that runs bcl2fastq and ease demultiplexing of Sequencing data"
authors = ["Sequana Team"]
license = "BSD-3"
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2 changes: 0 additions & 2 deletions requirements.txt

This file was deleted.

12 changes: 6 additions & 6 deletions sequana_pipelines/demultiplex/main.py
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Expand Up @@ -10,18 +10,18 @@
# documentation: http://sequana.readthedocs.io
#
##############################################################################
import sys
import os
import sys

import rich_click as click
import click_completion
import rich_click as click

click_completion.init()

NAME = "demultiplex"

from sequana_pipetools.options import *
from sequana_pipetools import SequanaManager
from sequana_pipetools.options import *

help = init_click(
NAME,
Expand All @@ -32,7 +32,7 @@


@click.command(context_settings=help)
@include_options_from(ClickSnakemakeOptions, working_directory=NAME)
@include_options_from(ClickSnakemakeOptions, working_directory="fastq")
@include_options_from(ClickSlurmOptions)
@include_options_from(ClickInputOptions, add_input_readtag=False)
@include_options_from(ClickGeneralOptions)
Expand Down Expand Up @@ -96,7 +96,7 @@
default=False,
is_flag=True,
show_default=True,
help="""Set options to--minimum-trimmed-read-length 15 --mask-short-adapter-reads 15
help="""Set options to--minimum-trimmed-read-length 15 --mask-short-adapter-reads 15
and do not merge lanes""",
)
@click.option(
Expand Down Expand Up @@ -190,7 +190,7 @@ def main(**options):
logger.critical(err)
logger.critical(
"""Your sample sheet seems to be incorrect. Before running the pipeline you will have to fix it. You may use 'sequana samplesheet --quick-fix'"""
)
)

# finalise the command and save it; copy the snakemake. update the config
# file and save it.
Expand Down

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