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release v0.5.0!
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CHANGELOG.md

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## [Unreleased]
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## [0.5.0] - 2021-03-03
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Version 0.5.0 brings many quality of life improvements, such as seq2science automatically inferring what needs to be re-run when changing the samples.tsv and/or the config.yaml, differential peak analysis for chip/atac workflows and tab-completion!
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To (hopefully) clear things up we changed the way technical and biological replicates are called, now technical and biological replicate, before technical replicate and condition.
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It is important to note that the RNA-seq workflow DOES NOT remove duplicate reads anymore as a *default*, and that the sc/bulk ATAC-seq workflows now filters reads on the nucleosome-free region as a *default*.
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### Changed
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- Keep all duplicate reads in RNA-seq by default
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First release of seq2science!
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[Unreleased]: https://github.com/vanheeringen-lab/seq2science/compare/master...v0.4.2
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[0.5.0]: https://github.com/vanheeringen-lab/seq2science/compare/v0.5.0...v0.4.3
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[0.4.3]: https://github.com/vanheeringen-lab/seq2science/compare/v0.4.3...v0.4.2
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[0.4.2]: https://github.com/vanheeringen-lab/seq2science/compare/v0.4.2...v0.4.1
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[0.4.1]: https://github.com/vanheeringen-lab/seq2science/compare/v0.4.1...v0.4.0

seq2science/__init__.py

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from . import util
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__all__ = ["util"]
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__version__ = "0.4.3"
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__version__ = "0.5.0"

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