Identification of somatic mutations in single cell DNA-seq using a spatial model of allelic imbalance
出版年份 2019 全文链接
标题
Identification of somatic mutations in single cell DNA-seq using a spatial model of allelic imbalance
作者
关键词
-
出版物
Nature Communications
Volume 10, Issue 1, Pages -
出版商
Springer Science and Business Media LLC
发表日期
2019-08-29
DOI
10.1038/s41467-019-11857-8
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Linked-read analysis identifies mutations in single-cell DNA-sequencing data
- (2019) Craig L. Bohrson et al. NATURE GENETICS
- COSMIC: the Catalogue Of Somatic Mutations In Cancer
- (2018) John G Tate et al. NUCLEIC ACIDS RESEARCH
- Accurate identification of single-nucleotide variants in whole-genome-amplified single cells
- (2017) Xiao Dong et al. NATURE METHODS
- Aging and neurodegeneration are associated with increased mutations in single human neurons
- (2017) Michael A. Lodato et al. SCIENCE
- Tissue-specific mutation accumulation in human adult stem cells during life
- (2016) Francis Blokzijl et al. NATURE
- Monovar: single-nucleotide variant detection in single cells
- (2016) Hamim Zafar et al. NATURE METHODS
- Resolving rates of mutation in the brain using single-neuron genomics
- (2016) Gilad D Evrony et al. eLife
- Single-Cell Whole-Genome Amplification and Sequencing: Methodology and Applications
- (2015) Lei Huang et al. Annual Review of Genomics and Human Genetics
- Chromothripsis from DNA damage in micronuclei
- (2015) Cheng-Zhong Zhang et al. NATURE
- Combining tumor genome simulation with crowdsourcing to benchmark somatic single-nucleotide-variant detection
- (2015) Adam D Ewing et al. NATURE METHODS
- Interactive analysis and assessment of single-cell copy-number variations
- (2015) Tyler Garvin et al. NATURE METHODS
- Somatic mutation in single human neurons tracks developmental and transcriptional history
- (2015) M. A. Lodato et al. SCIENCE
- Calibrating genomic and allelic coverage bias in single-cell sequencing
- (2015) Cheng-Zhong Zhang et al. Nature Communications
- Clonal evolution in breast cancer revealed by single nucleus genome sequencing
- (2014) Yong Wang et al. NATURE
- A Quantitative Comparison of Single-Cell Whole Genome Amplification Methods
- (2014) Charles F. A. de Bourcy et al. PLoS One
- Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
- (2014) Olivier Delaneau et al. Nature Communications
- Signatures of mutational processes in human cancer
- (2013) Ludmil B. Alexandrov et al. NATURE
- Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples
- (2013) Kristian Cibulskis et al. NATURE BIOTECHNOLOGY
- Snakemake--a scalable bioinformatics workflow engine
- (2012) J. Koster et al. BIOINFORMATICS
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data
- (2011) H. Li BIOINFORMATICS
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- (2011) Mark A DePristo et al. NATURE GENETICS
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