CNV calling pipeline for low coverage single-cell whole genome sequencing data

Output Details

Pipeline for analyzing, filtering, and comparing copy number variations from single-cell whole genome sequencing data that were amplified using PicoPLEX, PTA, or droplet MDA.
Identifier (DOI)
10.5281/zenodo.8225214

Meet the Authors

  • Zeliha Gözde Turan, PhD

    Key Personnel: Team Voet

    University College London

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    Jonas Demeulemeester, PhD

    Key Personnel: Team Voet

    KU Leuven

  • Fritz Sedlazeck, PhD

    Key Personnel: Team Voet

    Baylor College of Medicine

  • Christos Proukakis, PhD

    Co-PI (Core Leadership): Team Voet

    University College London

Aligning Science Across Parkinson's
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