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MuClone: Somatic mutation detection and classification through probabilistic integration of clonal population structure

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/j.cell.2012.04.023openalex-snapshot
The Life History of 21 Breast Cancers
inferredcites →https://doi.org/10.1016/j.cell.2012.08.024openalex-snapshot
Genomic Landscape of Non-Small Cell Lung Cancer in Smokers and Never-Smokers
inferredcites →https://doi.org/10.1038/nature08489openalex-snapshot
Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution
inferredcites →https://doi.org/10.1038/nature09515openalex-snapshot
Distant metastasis occurs late during the genetic evolution of pancreatic cancer
inferredcites →https://doi.org/10.1038/nature13952openalex-snapshot
Dynamics of genomic clones in breast cancer patient xenografts at single-cell resolution
inferredcites →https://doi.org/10.1038/nbt.2514openalex-snapshot
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples
inferredcites →https://doi.org/10.1038/ng.3573openalex-snapshot
Divergent modes of clonal spread and intraperitoneal mixing in high-grade serous ovarian cancer
inferredcites →https://doi.org/10.1038/nmeth.2883openalex-snapshot
PyClone: statistical inference of clonal population structure in cancer
inferredcites →https://doi.org/10.1056/nejmoa1113205openalex-snapshot
Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion Sequencing
inferredcites →https://doi.org/10.1056/nejmoa1616288openalex-snapshot
Tracking the Evolution of Non–Small-Cell Lung Cancer
inferredcites →https://doi.org/10.1089/cmb.2013.0106openalex-snapshot
Inference of Tumor Phylogenies with Improved Somatic Mutation Discovery
inferredcites →https://doi.org/10.1093/bioinformatics/btp373openalex-snapshot
VarScan: variant detection in massively parallel sequencing of individual and pooled samples
inferredcites →https://doi.org/10.1093/bioinformatics/btq040openalex-snapshot
SNVMix: predicting single nucleotide variants from next-generation sequencing of tumors
inferredcites →https://doi.org/10.1093/bioinformatics/btr629openalex-snapshot
Feature-based classifiers for somatic mutation detection in tumour–normal paired sequencing data
inferredcites →https://doi.org/10.1093/bioinformatics/bts053openalex-snapshot
JointSNVMix: a probabilistic model for accurate detection of somatic mutations in normal/tumour paired next-generation sequencing data
inferredcites →https://doi.org/10.1093/bioinformatics/bts271openalex-snapshot
Strelka: accurate somatic small-variant calling from sequenced tumor–normal sample pairs
inferredcites →https://doi.org/10.1093/bioinformatics/btu755openalex-snapshot
SNV-PPILP: refined SNV calling for tumor data using perfect phylogenies and ILP
inferredcites →https://doi.org/10.1093/nar/gkv135openalex-snapshot
multiSNV: a probabilistic approach for improving detection of somatic point mutations from multiple related tumour samples
inferredcites →https://doi.org/10.1101/gr.107524.110openalex-snapshot
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
inferredcites →https://doi.org/10.1101/gr.180281.114openalex-snapshot
TITAN: inference of copy number architectures in clonal cell populations from tumor whole-genome sequence data
inferredcites →https://doi.org/10.1126/science.1253462openalex-snapshot
Spatial and temporal diversity in genomic instability processes defines lung cancer evolution
inferredcites →https://doi.org/10.1186/gb-2013-14-8-r90openalex-snapshot
Virmid: accurate detection of somatic mutations with sample impurity inference
inferredcites →https://doi.org/10.1186/s13059-014-0572-2openalex-snapshot
De novo assembly of bacterial transcriptomes from RNA-seq data
inferredcites →https://doi.org/10.1186/s13059-015-0592-6openalex-snapshot
BitPhylogeny: a probabilistic framework for reconstructing intra-tumor phylogenies
inferredcites →https://doi.org/10.1186/s13059-015-0602-8openalex-snapshot
PhyloWGS: Reconstructing subclonal composition and evolution from whole-genome sequencing of tumors
inferredcites →https://doi.org/10.1186/s13059-015-0647-8openalex-snapshot
Fast and scalable inference of multi-sample cancer lineages
inferredcites →https://doi.org/10.1371/journal.pmed.1002197openalex-snapshot
Histological Transformation and Progression in Follicular Lymphoma: A Clonal Evolution Study

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inferred← citeshttps://doi.org/10.1101/655605openalex-snapshot
Accuracy of somatic variant detection in multiregional tumor sequencing data
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