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Published July 30, 2025 | Version Version 1
Dataset Open

Inferring tumor absolute copy number and clonal substructure from single-cell chromatin accessibility

  • 1. Guangdong Academy of Medical Sciences and Medical Research Institute, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University
  • 2. Institute of Precision Medicine, The First Affiliated Hospital, Sun Yat-Sen University
  • 3. Department of Urology, The Affiliated Hospital of Qingdao University
  • 4. Department of Gynecological Radiotherapy, Harbin Medical University Cancer Hospital

Description

This dataset is part of our project focusing on inferring absolute copy numbers and quantifying subclonal structures using single-cell ATAC-seq data. We employed two datasets. These datasets originate from Qilu Hospital of Shandong University, with proper authorization obtained for data collection and usage.

  • Dataset 1: Two ccRCC (clear cell renal cell carcinoma) samples analyzed using single-cell ATAC sequencing(ccRCC1 and ccRCC2).
  • Dataset 2: Two ccRCC samples analyzed using single-cell multiomics sequencing (ccRCC3 and ccRCC4).

All four samples were derived from frozen tissues, dissociated, and sequenced following 10x Genomics protocols. The datasets provided here are pre-processed and filtered, containing:

  • 6,281 cells for ccRCC dataset from scATAC-seq,
  • 8,432 cells for ccRCC dataset from scMultiomic-seq

In addition, we also provide paired WGS data of ccRCC1, ccRCC3 and ccRCC4 to evaluate the consistency of our model with the copy number at the DNA-seq level.

This resource provides valuable insights for inferring absolute copy numbers and subclonal heterogeneity.

Files

ccRCC1_WGS_bincounts.csv

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Additional details

Identifiers

Software

Repository URL
https://github.com/ShaojunLab/TeaCNV
Programming language
R
Development Status
Active