Abstract Background High-throughput sequencing allows the detection and quantification of frequencies of somatic single nucleotide variants (SNV) in heterogeneous tumor cell populations. In some cases, the evolutionary history and population frequency of the subclonal lineages of tumor cells present in the sample can be reconstructed from these SNV frequency measurements. But automated methods to do this reconstruction are not available and the conditions under which reconstruction is possible have not been described. Results We describe the conditions under which the evolutionary history can be uniquely reconstructed from SNV freque...
Next generation sequencing (NGS) technology provides researchers an opportunity to study cancer gen...
Next generation sequencing (NGS) technology provides researchers an opportunity to study cancer gen...
An accurate phylogeny of a cancer tumour has the potential to shed light on numerous phenomena, such...
Abstract Background High-throughput sequencing allows...
<div><p>Recent improvements in next-generation sequencing of tumor samples and the ability to identi...
Tumours are composed of multiple subpopulations, each of which has its own genotype and phenotype. ...
Somatic single nucleotide variants (SNVs) are mutations resulting from the substitution of a single ...
Cancer is a complex and deadly disease that is caused by genetic lesions in somatic cells. Further r...
Somatic single nucleotide variants (SNVs) are mutations resulting from the substitution of a single ...
Intra-tumor heterogeneity presents itself through the evolution of subclones during cancer progressi...
Cancer is a complex and deadly disease that is caused by genetic lesions in somatic cells. Further r...
Emerging ultra-low coverage single-cell DNA sequencing (scDNA-seq) technologies have enabled high re...
Although the role of evolutionary process in cancer progression is widely accepted, increasing atten...
Tumour development has long been recognised as an evolutionary process during which cells accumulate...
Cancer is a genetic disease characterized by the emergence of genetically distinct populations of ce...
Next generation sequencing (NGS) technology provides researchers an opportunity to study cancer gen...
Next generation sequencing (NGS) technology provides researchers an opportunity to study cancer gen...
An accurate phylogeny of a cancer tumour has the potential to shed light on numerous phenomena, such...
Abstract Background High-throughput sequencing allows...
<div><p>Recent improvements in next-generation sequencing of tumor samples and the ability to identi...
Tumours are composed of multiple subpopulations, each of which has its own genotype and phenotype. ...
Somatic single nucleotide variants (SNVs) are mutations resulting from the substitution of a single ...
Cancer is a complex and deadly disease that is caused by genetic lesions in somatic cells. Further r...
Somatic single nucleotide variants (SNVs) are mutations resulting from the substitution of a single ...
Intra-tumor heterogeneity presents itself through the evolution of subclones during cancer progressi...
Cancer is a complex and deadly disease that is caused by genetic lesions in somatic cells. Further r...
Emerging ultra-low coverage single-cell DNA sequencing (scDNA-seq) technologies have enabled high re...
Although the role of evolutionary process in cancer progression is widely accepted, increasing atten...
Tumour development has long been recognised as an evolutionary process during which cells accumulate...
Cancer is a genetic disease characterized by the emergence of genetically distinct populations of ce...
Next generation sequencing (NGS) technology provides researchers an opportunity to study cancer gen...
Next generation sequencing (NGS) technology provides researchers an opportunity to study cancer gen...
An accurate phylogeny of a cancer tumour has the potential to shed light on numerous phenomena, such...