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        <datestamp>2026-10-02T05:26:58Z</datestamp>
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          <dc:title>Bioinformatic pipeline for the analysis of single-cell whole-genome sequencing (scWGS) data</dc:title>
          <dc:creator>Alexander Wolff (25156302)</dc:creator>
          <dc:subject>Bioinformatic methods development</dc:subject>
          <dc:subject>scWGS</dc:subject>
          <dc:subject>;Aneuploidy</dc:subject>
          <dc:subject>bioinformatics</dc:subject>
          <dc:description>&lt;p dir="ltr"&gt;Bioinformatic pipeline for the analysis of single-cell whole-genome sequencing (scWGS) data. The pipeline uses Snakemake as a workflow manager to implement different tools and custom R scripts for the analysis of aneuploidy and copy number alterations using AneuFinder. The code was used in the manuscript entitled “BTRR complex deficiency is a driver for genomic instability in Bloom syndrome.”&lt;/p&gt;</dc:description>
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