Exploring Current Challenges and Perspectives for Automatic Reconstruction of Clonal Evolution

In the field of cancer research, reconstructing clonal evolution is of major interest. The technique provides new insights for analysis and prediction of tumor development. However, reconstruction based on mutational data is characterized by several challenges. By performing extensive literature res...

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Vydané v:Cancer genomics & proteomics Ročník 19; číslo 2; s. 194
Hlavní autori: Sandmann, Sarah, Richter, Silja, Jiang, Xiaoyi, Varghese, Julian
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Greece 01.03.2022
Predmet:
Algorithms
Clonal Evolution - genetics
Cluster Analysis
Computer Simulation
Humans
Phylogeny
Clonal evolution
tree reconstruction
variant integration
visualization
clustering
ISSN:1790-6245, 1790-6245
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Shrnutí:In the field of cancer research, reconstructing clonal evolution is of major interest. The technique provides new insights for analysis and prediction of tumor development. However, reconstruction based on mutational data is characterized by several challenges. By performing extensive literature research, we identified 51 currently available tools for reconstructing clonal evolution. By analyzing two cancer data sets (n=21), we investigated the applicability and performance of each tool. Seventeen out of 51 tools could be applied to our data. Correct clustering of variants can be observed for 4 patients in the presence of ≤3 clusters and ≥5 time points. Correct phylogenetic trees are determined for 10 patients. Accurate visualization is possible, by applying adjustments to the original algorithms. Despite bearing considerable potential, automatic reconstruction of clonal evolution remains challenging. To replace tedious manual reconstruction, further research including systematic error analyses using simulation tools needs to be conducted.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1790-6245
1790-6245
DOI:10.21873/cgp.20314