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Single-cell somatic copy number variants in brain using different amplification methods and reference genomes

By Ester Kalef-Ezra, Zeliha Gözde Turan, Diego Perez-Rodriguez:, Ida Bomann, Sairam Behera, Caoimhe Morley, Sonja W. Scholz, Zane Jaunmuktane, MD, Jonas Demeulemeester, Fritz Sedlazeck, Christos Proukakis, PhD
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Output Details

Description
This dataset contains 224 paired fastq files (112 single cells) from the following samples: brains from two Multiple System Atrophy patients and one control, and non-brain controls (fibroblasts, NA12878).
Tags
  • Brain
  • DNA WGS
  • Human
  • MSA (Multiple system atrophy)
  • Postmortem
Discovery Team
Team Voet
Program
Collaborative Research Network
Theme
PD Functional Genomics

Meet the Authors

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    Ester Kalef-Ezra

    External Collaborator

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    Zeliha Gözde Turan

    External Collaborator

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    Diego Perez-Rodriguez:

    External Collaborator

  • User avatar fallback logo

    Ida Bomann

    External Collaborator

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    Sairam Behera

    External Collaborator

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    Caoimhe Morley

    External Collaborator

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    Sonja W. Scholz

    External Collaborator

  • Zane Jaunmuktane, MD

    Co-PI (Core Leadership): Team Hardy,  Team Voet,  Team Wood, 

    University College London

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    Jonas Demeulemeester

    External Collaborator

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    Fritz Sedlazeck

    External Collaborator

  • Christos Proukakis, PhD

    Co-PI (Core Leadership): Team Voet, 

    University College London

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Aligning Science Across Parkinson's
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