A machine learning method for the discovery of minimum marker gene combinations for cell type identification from single-cell RNA sequencing.
A machine learning method for the discovery of minimum marker gene combinations for cell type identification from single-cell RNA sequencing.
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DOI:
10.1101/gr.275569.121
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发表时间:
2021-10
期刊:
影响因子:
7
通讯作者:
Scheuermann RH
中科院分区:
文献类型:
--
作者:
Aevermann B;Zhang Y;Novotny M;Keshk M;Bakken T;Miller J;Hodge R;Lelieveldt B;Lein E;Scheuermann RH
Single-cell genomics is rapidly advancing our knowledge of the diversity of cell phenotypes, including both cell types and cell states. Driven by single-cell/-nucleus RNA sequencing (scRNA-seq), comprehensive cell atlas projects characterizing a wide range of organisms and tissues are currently underway. As a result, it is critical that the transcriptional phenotypes discovered are defined and disseminated in a consistent and concise manner. Molecular biomarkers have historically played an important role in biological research, from defining immune cell types by surface protein expression to defining diseases by their molecular drivers. Here, we describe a machine learning-based marker gene selection algorithm, NS-Forest version 2.0, which leverages the nonlinear attributes of random forest feature selection and a binary expression scoring approach to discover the minimal marker gene expression combinations that optimally capture the cell type identity represented in complete scRNA-seq transcriptional profiles. The marker genes selected provide an expression barcode that serves as both a useful tool for downstream biological investigation and the necessary and sufficient characteristics for semantic cell type definition. The use of NS-Forest to identify marker genes for human brain middle temporal gyrus cell types reveals the importance of cell signaling and noncoding RNAs in neuronal cell type identity.
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影响因子:
64.5
作者:
Enge M;Arda HE;Mignardi M;Beausang J;Bottino R;Kim SK;Quake SR
通讯作者:
Quake SR
影响因子:
14.8
作者:
Krishnaswami SR;Grindberg RV;Novotny M;Venepally P;Lacar B;Bhutani K;Linker SB;Pham S;Erwin JA;Miller JA;Hodge R;McCarthy JK;Kelder M;McCorrison J;Aevermann BD;Fuertes FD;Scheuermann RH;Lee J;Lein ES;Schork N;McConnell MJ;Gage FH;Lasken RS
通讯作者:
Lasken RS
影响因子:
18.4
作者:
Levitin HM;Yuan J;Sims PA
通讯作者:
Sims PA
DOI:
10.1073/pnas.1507125112
发表时间:
2015-06-09
影响因子:
11.1
作者:
Darmanis S;Sloan SA;Zhang Y;Enge M;Caneda C;Shuer LM;Hayden Gephart MG;Barres BA;Quake SR
通讯作者:
Quake SR
影响因子:
64.5
作者:
Asp, Michaela;Giacomello, Stefania;Lundeberg, Joakim
通讯作者:
Lundeberg, Joakim