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@@ -14,7 +15,7 @@ A [Snakemake 8](https://snakemake.readthedocs.io/en/stable/) workflow to fetch (
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> ⭐️ **Star and share modules you find valuable** 📤 - help others discover them, and guide our future work!
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> [!IMPORTANT]
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> **If you use this workflow in a publication, please don't forget to give credit to the authors by citing it using this DOI [10.5281/zenodo.XXXXXX](https://doi.org/10.5281/zenodo.XXXXXX).**
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> **If you use this workflow in a publication, please don't forget to give credit to the authors by citing it using this DOI [10.5281/zenodo.15005419](https://doi.org/10.5281/zenodo.15005419).**
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__Data Acquisition & Processing.__ Public sequencing data were retrieved from [GSA|SRA|ENA|DDBJ] under the accession(s) [accession_ids] using iSeq (ver) [ref]. The data were downloaded as FASTQ files (and converted to unmapped BAM ([uBAM](https://gatk.broadinstitute.org/hc/en-us/articles/360035532132-uBAM-Unmapped-BAM-Format)) files using Picard FastqToSam (ver) [ref], preserving sample information and read groups while supporting both single-end and paired-end sequencing data). Metadata for each dataset was collected and merged into a single Comprehensive reference file.
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**The data acquisition and processing described here were performed using a publicly available Snakemake (ver) [ref] workflow [ref - cite this workflow here].**
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**The data acquisition and processing described here were performed using a publicly available Snakemake (ver) [ref] workflow [10.5281/zenodo.15005419](https://doi.org/10.5281/zenodo.15005419).**
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# 🚀 Features
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The workflow performs the following steps that produce the outlined results:
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