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Copy file name to clipboardExpand all lines: slides/creators/A_First_Workflow.tex
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The next step in our workflow will aggregate the mapped reads from all samples and jointly call genomic variants on them. We need two tools: \lhref{https://www.htslib.org/}{samtools} and \lhref{https://www.htslib.org/}{bcftools}. \newline\pause
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\Snakemake{} provides a helper function for collecting input files that helps us to describe the aggregation in this step. With
we obtain a list where the given pattern \altverb{sorted_reads/\{sample\}.bam} was formatted with the values in a given list of samples \altverb{SAMPLES}, i.\,e.
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we obtain a list where the given pattern \altverb{sorted_reads/\{sample\}.bam} was formatted with the values in a given list of samples \altverb{samples}, i.\,e.
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