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Copy file name to clipboardExpand all lines: workflows/variant-calling/ploidy-aware-genotype-calling/CHANGELOG.md
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# Changelog
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## [0.1.2] - 2026-03-16
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### Automatic update
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-`toolshed.g2.bx.psu.edu/repos/devteam/samtools_stats/samtools_stats/2.0.8` was updated to `toolshed.g2.bx.psu.edu/repos/devteam/samtools_stats/samtools_stats/2.0.9`
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## [0.1.1] 2026-03-12
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Copy file name to clipboardExpand all lines: workflows/variant-calling/ploidy-aware-genotype-calling/genotype-variant-calling-wgs-pe.ga
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{
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"child_steps": [
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],
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"color": "blue",
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],
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"format-version": "0.1",
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"license": "MIT",
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"release": "0.1.1",
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"name": "Paired end variant and ploidy-aware genotype calling",
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"readme": "This workflow performs end-to-end germline variant and genotype calling on paired-end Illumina sequencing data from organisms of any given ploidy. Starting from raw FASTQ reads, the workflow handles quality control, read mapping, duplicate removal, variant and genotype calling with FreeBayes, and functional annotation of the resulting variants.",
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