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Phylogenetic inference from single-cell RNA-seq data
DOI:10.1038/s41598-023-39995-6.png)
摘要
En 中文
Tumors are comprised of subpopulations of cancer cells that harbor distinct genetic profiles and phenotypes that evolve over time and during treatment. By reconstructing the course of cancer evolution, we can understand the acquisition of the malignant properties that drive tumor progression. Unfortunately, recovering the evolutionary relationships of individual cancer cells linked to their phenotypes remains a difficult challenge. To address this need, we have developed PhylinSic, a method that reconstructs the phylogenetic relationships among cells linked to their gene expression profiles from single cell RNA-sequencing (scRNA-Seq) data. This method calls nucleotide bases using a probabilistic smoothing approach and then estimates a phylogenetic tree using a Bayesian modeling algorithm. We showed that PhylinSic identified evolutionary relationships underpinning drug selection and metastasis and was sensitive enough to identify subclones from genetic drift. We found that breast cancer tumors resistant to chemotherapies harbored multiple genetic lineages that independently acquired high K-Ras and & beta;-catenin, suggesting that therapeutic strategies may need to control multiple lineages to be durable. These results demonstrated that PhylinSic can reconstruct evolution and link the genotypes and phenotypes of cells across monophyletic tumors using scRNA-Seq.
Keyword:
INTRATUMOR HETEROGENEITY
CLONAL EVOLUTION
SIGNATURES
EXPRESSION
GENOME
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期刊
IF:
3.9
论文数:
28.2W
被引数:
83.5W
机构
引用论文
clonealign: statistical integration of independent single-cell RNA and DNA sequencing data from human cancers
GENOME BIOLOGY
IF9.4
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data基因组分析工具包: 用于分析下一代DNA测序数据的MapReduce框架
GENOME RESEARCH
IF5.5
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing dataANNOVAR: 来自高通量测序数据的遗传变异的功能注释
NUCLEIC ACIDS RESEARCH
IF13.1
Bayesian coalescent inference of past population dynamics from molecular sequences从分子序列对过去种群动力学的贝叶斯合并推断

