标题
Accurate genotyping across variant classes and lengths using variant graphs
作者
关键词
-
出版物
NATURE GENETICS
Volume 50, Issue 7, Pages 1054-1059
出版商
Springer Nature
发表日期
2018-06-15
DOI
10.1038/s41588-018-0145-5
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。- Genome graphs and the evolution of genome inference
- (2017) Benedict Paten et al. GENOME RESEARCH
- Sequencing and de novo assembly of 150 genomes from Denmark as a population reference
- (2017) Lasse Maretty et al. NATURE
- Graphtyper enables population-scale genotyping using pangenome graphs
- (2017) Hannes P Eggertsson et al. NATURE GENETICS
- The impact of structural variation on human gene expression
- (2017) Colby Chiang et al. NATURE GENETICS
- A convex optimization approach for identification of human tissue-specific interactomes
- (2016) Shahin Mohammadi et al. BIOINFORMATICS
- A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigree
- (2016) Michael A. Eberle et al. GENOME RESEARCH
- KMC 2: fast and resource-frugal k-mer counting
- (2015) Sebastian Deorowicz et al. BIOINFORMATICS
- An integrated map of structural variation in 2,504 human genomes
- (2015) Peter H. Sudmant et al. NATURE
- A global reference for human genetic variation
- (2015) Richard A. Gibbs et al. NATURE
- Improved genome inference in the MHC using a population reference graph
- (2015) Alexander Dilthey et al. NATURE GENETICS
- Large multiallelic copy number variations in humans
- (2015) Robert E Handsaker et al. NATURE GENETICS
- SpeedSeq: ultra-fast personal genome analysis and interpretation
- (2015) Colby Chiang et al. NATURE METHODS
- Indexing Graphs for Path Queries with Applications in Genome Research
- (2014) Jouni Siren et al. IEEE-ACM Transactions on Computational Biology and Bioinformatics
- Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls
- (2014) Justin M Zook et al. NATURE BIOTECHNOLOGY
- Whole-genome sequence variation, population structure and demographic history of the Dutch population
- (2014) Laurent C Francioli et al. NATURE GENETICS
- Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications
- (2014) Andy Rimmer et al. NATURE GENETICS
- Short read alignment with populations of genomes
- (2013) L. Huang et al. BIOINFORMATICS
- CrossMap: a versatile tool for coordinate conversion between genome assemblies
- (2013) Hao Zhao et al. BIOINFORMATICS
- pIRS: Profile-based Illumina pair-end reads simulator
- (2012) Xuesong Hu et al. BIOINFORMATICS
- De novo assembly and genotyping of variants using colored de Bruijn graphs
- (2012) Zamin Iqbal et al. NATURE GENETICS
- 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
- Dindel: Accurate indel calls from short-read data
- (2010) C. A. Albers et al. GENOME RESEARCH
- The Sequence Alignment/Map format and SAMtools
- (2009) H. Li et al. BIOINFORMATICS
- Simultaneous alignment of short reads against multiple genomes
- (2009) Korbinian Schneeberger et al. GENOME BIOLOGY
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started