gCAnno: a graph-based single cell type annotation method

Background Current single cell analysis methods annotate cell types at cluster-level rather than ideally at single cell level. Multiple exchangeable clustering methods and many tunable parameters have a substantial impact on the clustering outcome, often leading to incorrect cluster-level annotation...

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Published inBMC genomics Vol. 21; no. 1; p. 823
Main Authors Yang, Xiaofei, Gao, Shenghan, Wang, Tingjie, Yang, Boyu, Dang, Ningxin, Ye, Kai
Format Journal Article
LanguageEnglish
Published London BioMed Central 23.11.2020
BioMed Central Ltd
Springer Nature B.V
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Online AccessGet full text
ISSN1471-2164
1471-2164
DOI10.1186/s12864-020-07223-4

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Summary:Background Current single cell analysis methods annotate cell types at cluster-level rather than ideally at single cell level. Multiple exchangeable clustering methods and many tunable parameters have a substantial impact on the clustering outcome, often leading to incorrect cluster-level annotation or multiple runs of subsequent clustering steps. To address these limitations, methods based on well-annotated reference atlas has been proposed. However, these methods are currently not robust enough to handle datasets with different noise levels or from different platforms. Results Here, we present gCAnno, a graph-based Cell type Annotation method. First, gCAnno constructs cell type-gene bipartite graph and adopts graph embedding to obtain cell type specific genes. Then, naïve Bayes (gCAnno-Bayes) and SVM (gCAnno-SVM) classifiers are built for annotation. We compared the performance of gCAnno to other state-of-art methods on multiple single cell datasets, either with various noise levels or from different platforms. The results showed that gCAnno outperforms other state-of-art methods with higher accuracy and robustness. Conclusions gCAnno is a robust and accurate cell type annotation tool for single cell RNA analysis. The source code of gCAnno is publicly available at https://github.com/xjtu-omics/gCAnno .
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ISSN:1471-2164
1471-2164
DOI:10.1186/s12864-020-07223-4