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Merge pull request #536 from nf-core/patch
Patch release 2.0.1
2 parents 752a9e1 + 21658fb commit 1489b71

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CHANGELOG.md

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The format is based on [Keep a Changelog](https://keepachangelog.com/en/1.0.0/)
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and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0.html).
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## 2.0.1 - Asterix (Patch) [2024-03-25]
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### `Fixed`
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- Germlinecnvcaller subworkflow uses the output channel `casecalls` from germlinecnvcaller module instead of `calls` which was invalid. [#535](https://github.com/nf-core/raredisease/issues/535)
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## 2.0.0 - Asterix [2024-03-18]
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### `Added`

assets/multiqc_config.yml

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custom_logo_title: "nf-core/raredisease"
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report_comment: >
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This report has been generated by the <a href="https://github.com/nf-core/raredisease/releases/tag/2.0.0" target="_blank">nf-core/raredisease</a>
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This report has been generated by the <a href="https://github.com/nf-core/raredisease/releases/tag/2.0.1" target="_blank">nf-core/raredisease</a>
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analysis pipeline. For information about how to interpret these results, please see the
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<a href="https://nf-co.re/raredisease/2.0.0/docs/output" target="_blank">documentation</a>.
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<a href="https://nf-co.re/raredisease/2.0.1/docs/output" target="_blank">documentation</a>.
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report_section_order:
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"nf-core-raredisease-methods-description":
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order: -1000

nextflow.config

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description = """call and score variants from WGS/WES of rare disease patients"""
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mainScript = 'main.nf'
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nextflowVersion = '!>=23.04.0'
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version = '2.0.0'
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version = '2.0.1'
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doi = ''
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}
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subworkflows/local/variant_calling/call_sv_germlinecnvcaller.nf

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GATK4_GERMLINECNVCALLER ( ch_gcnvc_in )
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GATK4_GERMLINECNVCALLER.out.calls.toList()
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GATK4_GERMLINECNVCALLER.out.casecalls.toList()
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.flatMap {reduce_input(it)}
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.buffer (size: 2)
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.combine(ch_gcnvcaller_model.collect{it[1]}.toList())

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