PO.TB05.03 · 肿瘤生物学
通过更新的细胞类型注释、CNV推断和可视化工具提升单细胞儿童癌症图谱的实用性
Improving the utility of the single-cell pediatric cancer atlas through updated cell type annotations, CNV inference, and visualization tools
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
单细胞儿童癌症图谱(ScPCA)门户(https://scpca.alexslemonade.org/)由儿童癌症数据实验室(Childhood Cancer Data Lab)开发和维护,是一个数据资源,提供统一处理的单细胞和单核RNA测序数据,以及来自儿童肿瘤样本的去标识化元数据。该门户最初由Alex's Lemonade Stand基金会(ALSF)资助的10个项目的数据组成,目前包含来自ALSF资助和社区贡献数据集的、涵盖50多种癌症类型的700多个样本的汇总基因表达数据。下载内容包括作为SingleCellExperiment或AnnData对象的基因表达数据,含原始和标准化计数、PCA和UMAP坐标以及汇总报告。部分样本在下载中包含来自bulk RNA-seq、空间转录组学和/或特征条形码(例如CITE-seq和细胞哈希)的额外数据。门户上的所有数据均使用scpca-nf进行统一处理,这是一个由数据实验室编写和维护的高效开源Nextflow工作流,利用alevin-fry来量化基因表达。
自2024年AACR年会展示ScPCA门户以来,可用数据中新增了若干功能。现使用三种独特方法进行自动细胞类型注释:SingleR、CellAssign和SCimilarity。若三种方法中有两种一致,则分配一个本体感知的共识细胞类型标签。各项单独注释和共识细胞类型都包含在下载对象的细胞元数据中。部分项目还包括作为OpenScPCA项目(https://openscpca.readthedocs.io)一部分生成的人工整理的细胞类型注释。
此外,现使用InferCNV软件包对每个样本进行拷贝数变异(CNV)推断,指定i6 HMM来量化特定的CNV事件。由于InferCNV使用一组指定的正常或非恶性参考细胞来量化CNV事件,因此使用共识细胞类型为每个样本识别与诊断相适应的正常细胞参考。观察到的CNV总数和完整的HMM元数据表存储在处理后的SingleCellExperiment和AnnData对象中。更新的细胞类型注释和InferCNV的实现被纳入开源工作流scpca-nf。该工作流及相关文档可在https://github.com/AlexsLemonade/scpca-nf免费获取。
最后,ScPCA门户托管了一个UCSC Cell Browser实例,使用户无需下载数据即可可视化并交互所有样本的基因表达数据。关于数据处理和门户上文件内容的全面文档,包括开始使用ScPCA数据集的指南,可在https://scpca.readthedocs.io找到。
查看英文原文 English abstract
The Single-cell Pediatric Cancer Atlas (ScPCA) Portal (https://scpca.alexslemonade.org/), developed and maintained by the Childhood Cancer Data Lab, is a data resource for uniformly processed single-cell and single-nuclei RNA sequencing data, as well as de-identified metadata from pediatric tumor samples. Originally comprised of data from 10 projects funded by Alex's Lemonade Stand Foundation (ALSF), the Portal currently contains summarized gene expression data for over 700 samples across more than 50 cancer types drawn from ALSF-funded and community-contributed datasets. Downloads include gene expression data as SingleCellExperiment or AnnData objects containing raw and normalized counts, PCA and UMAP coordinates, and summary reports. Some samples have additional data from bulk RNA-seq, spatial transcriptomics, and/or feature barcoding (e.g., CITE-seq and cell hashing) included in the download. All data on the Portal were uniformly processed using scpca-nf, an efficient and open-source Nextflow workflow written and maintained by the Data Lab, which utilizes alevin-fry to quantify gene expression.
Since presenting the ScPCA Portal at the 2024 AACR Annual Meeting, several new features have been added to the available data. Automated cell type annotation is now performed using three unique methods: SingleR, CellAssign, and SCimilarity. If two of the three methods agree, an ontology-aware consensus cell type label is assigned. The individual annotations and the consensus cell types are included in the cell metadata of the downloaded objects. Some projects also include manually-curated cell type annotations generated as part of the OpenScPCA project (https://openscpca.readthedocs.io).
In addition, copy-number variation (CNV) inference is now performed on each sample using the InferCNV package, specifying the i6 HMM to quantify specific CNV events. Since InferCNV quantifies CNV events using a designated set of normal, or non-malignant, reference cells, consensus cell types are used to identify a diagnosis-appropriate normal cell reference for each sample. The total CNVs observed and the full HMM metadata table are stored in the processed SingleCellExperiment and AnnData objects. The updated cell type annotation and implementation of InferCNV are included as part of the open-source workflow, scpca-nf. The workflow and associated documentation are freely available at https://github.com/AlexsLemonade/scpca-nf.
Finally, the ScPCA Portal hosts an instance of the UCSC Cell Browser, enabling users to visualize and interact with the gene expression data for all samples without needing to download the data. Comprehensive documentation about data processing and the contents of files on the portal, including a guide to getting started working with an ScPCA dataset, can be found at https://scpca.readthedocs.io.
利益披露 Disclosure
A. G. Hawkins, None..
J. A. Shapiro, None..
S. J. Spielman, None..
D. S. Mejia, None..
D. Venkatesh Prasad, None..
N. Ichihara, None..
A. Yakovets, None..
A. M. Gottlieb, None..
K. G. Wheeler, None..
C. J. Bethell, None..
S. M. Foltz, None..
J. O'Malley, None..
J. N. Taroni, None.