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

View Published Dataset

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

Ester Kalef-Ezra

External Collaborator
Zeliha Gözde Turan

External Collaborator
Diego Perez-Rodriguez:

External Collaborator
Ida Bomann

External Collaborator
Sairam Behera

External Collaborator
Caoimhe Morley

External Collaborator
Sonja W. Scholz

External Collaborator
Zane Jaunmuktane, MD

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

University College London
Jonas Demeulemeester

External Collaborator
Fritz Sedlazeck

External Collaborator
Christos Proukakis, PhD

Co-PI (Core Leadership): Team Voet,

University College London

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

Output Details

Meet the Authors

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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