CDSeq: A novel complete deconvolution method for dissecting heterogeneous samples using gene expression data

39Citations
Citations of this article
159Readers
Mendeley users who have this article in their library.

Abstract

Quantifying cell-type proportions and their corresponding gene expression profiles in tissue samples would enhance understanding of the contributions of individual cell types to the physiological states of the tissue. Current approaches that address tissue heterogeneity have drawbacks. Experimental techniques, such as fluorescence-activated cell sorting, and single cell RNA sequencing are expensive. Computational approaches that use expression data from heterogeneous samples are promising, but most of the current methods estimate either cell-type proportions or cell-type-specific expression profiles by requiring the other as input. Although such partial deconvolution methods have been successfully applied to tumor samples, the additional input required may be unavailable. We introduce a novel complete deconvolution method, CDSeq, that uses only RNA-Seq data from bulk tissue samples to simultaneously estimate both cell-type proportions and cell-type-specific expression profiles. Using several synthetic and real experimental datasets with known cell-type composition and cell-type-specific expression profiles, we compared CDSeq’s complete deconvolution performance with seven other established deconvolution methods. Complete deconvolution using CDSeq represents a substantial technical advance over partial deconvolution approaches and will be useful for studying cell mixtures in tissue samples. CDSeq is available at GitHub repository (MATLAB and Octave code): https://github.com/kkang7/ CDSeq.

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Kang, K., Meng, Q., Shats, I., Umbach, D. M., Li, M., Li, Y., … Li, L. (2019). CDSeq: A novel complete deconvolution method for dissecting heterogeneous samples using gene expression data. PLoS Computational Biology, 15(12). https://doi.org/10.1371/journal.pcbi.1007510

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 55

54%

Researcher 39

38%

Professor / Associate Prof. 6

6%

Lecturer / Post doc 2

2%

Readers' Discipline

Tooltip

Biochemistry, Genetics and Molecular Bi... 43

50%

Agricultural and Biological Sciences 25

29%

Computer Science 11

13%

Medicine and Dentistry 7

8%

Article Metrics

Tooltip
Mentions
Blog Mentions: 1
References: 1

Save time finding and organizing research with Mendeley

Sign up for free