标题
Monovar: single-nucleotide variant detection in single cells
作者
关键词
-
出版物
NATURE METHODS
Volume 13, Issue 6, Pages 505-507
出版商
Springer Nature
发表日期
2016-04-19
DOI
10.1038/nmeth.3835
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。- Droplet Barcoding for Single-Cell Transcriptomics Applied to Embryonic Stem Cells
- (2015) Allon M. Klein et al. CELL
- Highly Parallel Genome-wide Expression Profiling of Individual Cells Using Nanoliter Droplets
- (2015) Evan Z. Macosko et al. CELL
- The first five years of single-cell cancer genomics and beyond
- (2015) Nicholas E. Navin GENOME RESEARCH
- Advances and Applications of Single-Cell Sequencing Technologies
- (2015) Yong Wang et al. MOLECULAR CELL
- Interactive analysis and assessment of single-cell copy-number variations
- (2015) Tyler Garvin et al. NATURE METHODS
- Computational and analytical challenges in single-cell transcriptomics
- (2015) Oliver Stegle et al. NATURE REVIEWS GENETICS
- SNES: single nucleus exome sequencing
- (2015) Marco L Leung et al. GENOME BIOLOGY
- Clonal evolution in breast cancer revealed by single nucleus genome sequencing
- (2014) Yong Wang et al. NATURE
- COSMIC: exploring the world's knowledge of somatic mutations in human cancer
- (2014) Simon A. Forbes et al. NUCLEIC ACIDS RESEARCH
- Dissecting the clonal origins of childhood acute lymphoblastic leukemia by single-cell genomics
- (2014) Charles Gawad et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Accounting for technical noise in single-cell RNA-seq experiments
- (2013) Philip Brennecke et al. NATURE METHODS
- SNP calling using genotype model selection on high-throughput sequencing data
- (2012) Na You et al. BIOINFORMATICS
- Genome-wide Single-Cell Analysis of Recombination Activity and De Novo Mutation Rates in Human Sperm
- (2012) Jianbin Wang et al. CELL
- VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
- (2012) D. C. Koboldt et al. GENOME RESEARCH
- SNP Calling, Genotype Calling, and Sample Allele Frequency Estimation from New-Generation Sequencing Data
- (2012) Rasmus Nielsen et al. PLoS One
- Genome-Wide Detection of Single-Nucleotide and Copy-Number Variations of a Single Human Cell
- (2012) C. Zong et al. SCIENCE
- Single-cell sequencing analysis characterizes common and cell-lineage-specific mutations in a muscle-invasive bladder cancer
- (2012) Yingrui Li et al. GigaScience
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data
- (2011) H. Li BIOINFORMATICS
- Tumour evolution inferred by single-cell sequencing
- (2011) Nicholas Navin et al. NATURE
- SNVMix: predicting single nucleotide variants from next-generation sequencing of tumors
- (2010) Rodrigo Goya et al. BIOINFORMATICS
- BEDTools: a flexible suite of utilities for comparing genomic features
- (2010) Aaron R. Quinlan et al. BIOINFORMATICS
- SNP detection and genotyping from low-coverage sequencing data on multiple diploid samples
- (2010) S. Q. Le et al. GENOME RESEARCH
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
- (2010) A. McKenna et al. GENOME RESEARCH
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
- SOAP2: an improved ultrafast tool for short read alignment
- (2009) R. Li et al. BIOINFORMATICS
- The Sequence Alignment/Map format and SAMtools
- (2009) H. Li et al. BIOINFORMATICS
- Fast and accurate short read alignment with Burrows-Wheeler transform
- (2009) H. Li et al. BIOINFORMATICS
- Human Triallelic Sites: Evidence for a New Mutational Mechanism?
- (2009) A. Hodgkinson et al. GENETICS
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now