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Accurate estimation of cell-type composition from gene expression data

Author

Listed:
  • Daphne Tsoucas

    (Dana-Farber Cancer Institute
    Harvard T.H. Chan School of Public Health)

  • Rui Dong

    (Dana-Farber Cancer Institute
    Harvard T.H. Chan School of Public Health)

  • Haide Chen

    (Zhejiang University School of Medicine)

  • Qian Zhu

    (Dana-Farber Cancer Institute
    Harvard T.H. Chan School of Public Health)

  • Guoji Guo

    (Zhejiang University School of Medicine)

  • Guo-Cheng Yuan

    (Dana-Farber Cancer Institute
    Harvard T.H. Chan School of Public Health)

Abstract

The rapid development of single-cell transcriptomic technologies has helped uncover the cellular heterogeneity within cell populations. However, bulk RNA-seq continues to be the main workhorse for quantifying gene expression levels due to technical simplicity and low cost. To most effectively extract information from bulk data given the new knowledge gained from single-cell methods, we have developed a novel algorithm to estimate the cell-type composition of bulk data from a single-cell RNA-seq-derived cell-type signature. Comparison with existing methods using various real RNA-seq data sets indicates that our new approach is more accurate and comprehensive than previous methods, especially for the estimation of rare cell types. More importantly, our method can detect cell-type composition changes in response to external perturbations, thereby providing a valuable, cost-effective method for dissecting the cell-type-specific effects of drug treatments or condition changes. As such, our method is applicable to a wide range of biological and clinical investigations.

Suggested Citation

  • Daphne Tsoucas & Rui Dong & Haide Chen & Qian Zhu & Guoji Guo & Guo-Cheng Yuan, 2019. "Accurate estimation of cell-type composition from gene expression data," Nature Communications, Nature, vol. 10(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-10802-z
    DOI: 10.1038/s41467-019-10802-z
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    Cited by:

    1. Gavin J. Sutton & Daniel Poppe & Rebecca K. Simmons & Kieran Walsh & Urwah Nawaz & Ryan Lister & Johann A. Gagnon-Bartsch & Irina Voineagu, 2022. "Comprehensive evaluation of deconvolution methods for human brain gene expression," Nature Communications, Nature, vol. 13(1), pages 1-18, December.
    2. Kieran Tebben & Salif Yirampo & Drissa Coulibaly & Abdoulaye K. Koné & Matthew B. Laurens & Emily M. Stucke & Ahmadou Dembélé & Youssouf Tolo & Karim Traoré & Amadou Niangaly & Andrea A. Berry & Boure, 2024. "Gene expression analyses reveal differences in children’s response to malaria according to their age," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    3. Akram A. Hamed & Daniel J. Kunz & Ibrahim El-Hamamy & Quang M. Trinh & Omar D. Subedar & Laura M. Richards & Warren Foltz & Garrett Bullivant & Matthaeus Ware & Maria C. Vladoiu & Jiao Zhang & Antony , 2022. "A brain precursor atlas reveals the acquisition of developmental-like states in adult cerebral tumours," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
    4. Yanshuo Chen & Yixuan Wang & Yuelong Chen & Yuqi Cheng & Yumeng Wei & Yunxiang Li & Jiuming Wang & Yingying Wei & Ting-Fung Chan & Yu Li, 2022. "Deep autoencoder for interpretable tissue-adaptive deconvolution and cell-type-specific gene analysis," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    5. Zhenzhen Xun & Xinyu Ding & Yao Zhang & Benyan Zhang & Shujing Lai & Duowu Zou & Junke Zheng & Guoqiang Chen & Bing Su & Leng Han & Youqiong Ye, 2023. "Reconstruction of the tumor spatial microenvironment along the malignant-boundary-nonmalignant axis," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    6. Xiaoyu Song & Jiayi Ji & Joseph H. Rothstein & Stacey E. Alexeeff & Lori C. Sakoda & Adriana Sistig & Ninah Achacoso & Eric Jorgenson & Alice S. Whittemore & Robert J. Klein & Laurel A. Habel & Pei Wa, 2023. "MiXcan: a framework for cell-type-aware transcriptome-wide association studies with an application to breast cancer," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    7. Khoa A. Tran & Venkateswar Addala & Rebecca L. Johnston & David Lovell & Andrew Bradley & Lambros T. Koufariotis & Scott Wood & Sunny Z. Wu & Daniel Roden & Ghamdan Al-Eryani & Alexander Swarbrick & E, 2023. "Performance of tumour microenvironment deconvolution methods in breast cancer using single-cell simulated bulk mixtures," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
    8. Shijia Zhu & Naoto Kubota & Shidan Wang & Tao Wang & Guanghua Xiao & Yujin Hoshida, 2024. "STIE: Single-cell level deconvolution, convolution, and clustering in in situ capturing-based spatial transcriptomics," Nature Communications, Nature, vol. 15(1), pages 1-18, December.
    9. Jingtao Wang & Gregory J. Fonseca & Jun Ding, 2024. "scSemiProfiler: Advancing large-scale single-cell studies through semi-profiling with deep generative models and active learning," Nature Communications, Nature, vol. 15(1), pages 1-27, December.

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