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.bumpversion.cfg

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[bumpversion]
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current_version = 18.0.0
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current_version = 18.0.1
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commit = True
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tag = True
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tag_name = v{new_version}

BALSAMIC/__init__.py

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__version__ = "18.0.0"
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__version__ = "18.0.1"

BALSAMIC/__version__.py

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__version__ = "18.0.0"
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__version__ = "18.0.1"

CHANGELOG.rst

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[X.X.X]
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[18.0.1]
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--------
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CITATION.cff

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- family-names: "Wirta"
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given-names: "Valtteri"
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title: "BALSAMIC: Bioinformatic Analysis pipeLine for SomAtic MutatIons in Cancer"
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version: v18.0.0
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version: v18.0.1
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url: "https://github.com/Clinical-Genomics/BALSAMIC"

README.rst

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<a href="https://github.com/Clinical-Genomics/BALSAMIC">
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<img width=480 src="https://raw.githubusercontent.com/Clinical-Genomics/BALSAMIC/master/BALSAMIC/assets/images/balsamic_logo.png">
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</a>
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<h3 align="center">Bioinformatic Analysis pipeLine for SomAtic MutatIons in Cancer (v 18.0.0)</h3>
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<h3 align="center">Bioinformatic Analysis pipeLine for SomAtic MutatIons in Cancer (v 18.0.1)</h3>
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<h3 align="center">FastQ to Annotated VCF</h3>
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</p>
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.. |docker_latest_build_status| image:: https://github.com/Clinical-Genomics/BALSAMIC/actions/workflows/docker_build_push.yml/badge.svg
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.. |docker_latest_release_status| image:: https://github.com/Clinical-Genomics/BALSAMIC/actions/workflows/docker_build_push_release.yml/badge.svg?tag=v18.0.0
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.. |docker_latest_release_status| image:: https://github.com/Clinical-Genomics/BALSAMIC/actions/workflows/docker_build_push_release.yml/badge.svg?tag=v18.0.1
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.. |snakemake_badge| image:: https://img.shields.io/badge/snakemake-%E2%89%A55.12.3-brightgreen.svg
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docs/balsamic_methods.rst

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Target Genome Analysis
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~~~~~~~~~~~~~~~~~~~~~~
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BALSAMIC :superscript:`1` (**version** = 18.0.0) was used to analyze the data from raw FASTQ files.
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BALSAMIC :superscript:`1` (**version** = 18.0.1) was used to analyze the data from raw FASTQ files.
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We first quality controlled FASTQ files using FastQC v0.11.9 :superscript:`2`.
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Adapter sequences are trimmed using fastp v0.23.2 :superscript:`3` and then UMI sequences are extracted using the UMI extract tool from sentieon-tools (version 202308.03) :superscript:`15` and finally low-quality bases were trimmed using fastp v0.23.2 :superscript:`3`.
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Trimmed reads were mapped to the reference genome hg19 using sentieon-tools :superscript:`15`.
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Whole Genome Analysis
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~~~~~~~~~~~~~~~~~~~~~
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BALSAMIC :superscript:`1` (**version** = 18.0.0) was used to analyze the data from raw FASTQ files.
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BALSAMIC :superscript:`1` (**version** = 18.0.1) was used to analyze the data from raw FASTQ files.
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We first quality controlled FASTQ files using FastQC v0.11.9 :superscript:`2`.
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Adapter sequences and low-quality bases were trimmed using fastp v0.23.2 :superscript:`3`.
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Trimmed reads were mapped to the reference genome hg19 using sentieon-tools 202308.03 :superscript:`15`.
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UMI workflow
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~~~~~~~~~~~~~~~~~~~~~
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BALSAMIC :superscript:`1` (**version** = 18.0.0) was used to analyze the data from raw FASTQ files.
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BALSAMIC :superscript:`1` (**version** = 18.0.1) was used to analyze the data from raw FASTQ files.
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We first quality controlled FASTQ files using FastQC v0.11.9 :superscript:`2`.
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Adapter sequences were trimmed using fastp v0.23.2 :superscript:`3`.
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UMI tag extraction and alignment and consensus-calling of UMI groups were performed using Sentieon tools 202308.03 :superscript:`15`.

docs/bioinfo_softwares.rst

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Tools and software
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=================================
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BALSAMIC ( **version** = 18.0.0 ) uses myriad of tools and softwares to analyze fastq files. This section covers why each
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BALSAMIC ( **version** = 18.0.1 ) uses myriad of tools and softwares to analyze fastq files. This section covers why each
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one is included: usage and parameters, and relevant external links.
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ascatNgs

docs/install.rst

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Installation
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============
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This section describes steps to install BALSAMIC (**version** = 18.0.0)
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This section describes steps to install BALSAMIC (**version** = 18.0.1)
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docs/user_guide.rst

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Short tutorial
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==============
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Here a short tutorial is provided for BALSAMIC (**version** = 18.0.0).
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Here a short tutorial is provided for BALSAMIC (**version** = 18.0.1).
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Regarding fastq-inputs
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---------------------------

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