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Copy file name to clipboardExpand all lines: CHANGELOG.md
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### `Changed`
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-[#316](https://github.com/nf-core/epitopeprediction/pull/316) Added parameter `--biomart_dump` in `epaa.py` ([@SusiJo](https://github.com/SusiJo/)).
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-[#320](https://github.com/nf-core/epitopeprediction/pull/320) Set default genome reference to GRCh38 ([@jonasscheid](https://github.com/jonasscheid/)).
Copy file name to clipboardExpand all lines: docs/usage.md
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> [!IMPORTANT]
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> Please note that genomic variants have to be annotated. Currently, we support variants that have been annotated using [SnpEff](http://pcingola.> github.io/SnpEff/) and [VEP](https://www.ensembl.org/info/docs/tools/vep/index.html).
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For genomic variants, reference information from `Ensembl BioMart` is used. The default database version is the most recent `GRCh37` version. If you want to do the predictions based on `GRCh38` as the reference genome, please specify `--genome_reference grch38` in your pipeline call. You can also specify valid `Ensembl BioMart` archive version urls as `--genome_reference` value, e.g. [the archive version of December 2021](http://dec2021.archive.ensembl.org/).
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For genomic variants, reference information from `Ensembl BioMart` is used. The default database version is the most recent `GRCh38` version. If you want to do the predictions based on `GRCh37` as the reference genome, please specify `--genome_reference grch37` in your pipeline call. You can also specify valid `Ensembl BioMart` archive version urls as `--genome_reference` value, e.g. [the archive version of December 2021](http://dec2021.archive.ensembl.org/).
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> [!IMPORTANT]
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> Please note that old archive versions are regularly retired, therefore it might be possible that a used version is not available anymore at a later point.
Copy file name to clipboardExpand all lines: nextflow_schema.json
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},
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"genome_reference": {
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"type": "string",
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"default": "grch37",
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"default": "grch38",
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"help_text": "This defines against which human Ensembl genome reference the pipeline performs the analysis including the incorporation of genetic variants. If `grch37` or `grch38` are specified, the most recent Ensembl Biomart version for genome versions will be used. Alternatively, an Ensembl Biomart (archive) version can be specified, e.g. http://jan2020.archive.ensembl.org/.",
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"description": "Specifies the Ensembl genome reference version that will be used."
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