Accès ouvert
2026
dataset
OpenAlex
Katharina Schmid, Aikaterini Symeonidi, Dmytro Hlushchenko, Maria L. Richter et autres
This repository contains the ground truth CNV calls of 17 different datasets, as described in the publication "Benchmarking scRNA-seq copy number variation callers", Nature Communications 2025. The data was obtained from bulk WES, WGS and scWGS data. For the scWGS data, the …
de, nl, es
(code pays fourni par la source)
Accès ouvert
2026
dataset
OpenAlex
Katharina Schmid, Aikaterini Symeonidi, Dmytro Hlushchenko, Maria L. Richter et autres
This repository contains the ground truth CNV calls of 17 different datasets, as described in the publication "Benchmarking scRNA-seq copy number variation callers", Nature Communications 2025. The data was obtained from bulk WES, WGS and scWGS data. For the scWGS data, the …
de, nl, es
(code pays fourni par la source)
Accès ouvert
2025
article
OpenAlex
Katharina Schmid, Aikaterini Symeonidi, Dmytro Hlushchenko, Maria Lucia Richter et autres
Copy number variations (CNVs), the gain or loss of genomic regions, are associated with disease, especially cancer. Single cell technologies offer new possibilities to capture within-sample heterogeneity of CNVs and identify subclones relevant for tumor progression and treatment outcome. Several computational tools …
de, us, nl, es
(code pays fourni par la source)
Accès ouvert
2025
article
OpenAlex
Nabil E. Boutagy, Lorna Glenn, Bill Nave, O. Severinchik et autres
Purpose: Pancreas transplantation is a curative solution for patients with Type 1 Diabetes. However, less than 1000 pancreas transplantations are conducted each year due to a lack of suitable organs. Approximately 30% of pancreases procured from deceased donors in the United States …
us
(code pays fourni par la source)
2025
dataset
OpenAlex
Maria Lucia Richter, Katharina Schmid, Maria Colomé‐Tatché, Floris Foijer et autres
de, nl
(code pays fourni par la source)
Accès ouvert
2024
preprint
OpenAlex
Katharina Schmid, Aikaterini Symeonidi, Dmytro Hlushchenko, Maria Lucia Richter et autres
Abstract Copy number variations (CNVs), the gain or loss of genomic regions, are associated with different diseases and cancer types, where they are related to tumor progression and treatment outcome. Single cell technologies offer new possibilities to measure CNVs in individual cells, …
de
(code pays fourni par la source)