ViVar: A Comprehensive Platform for the Analysis and Visualization of Structural Genomic Variation
出版年份 2014 全文链接
标题
ViVar: A Comprehensive Platform for the Analysis and Visualization of Structural Genomic Variation
作者
关键词
-
出版物
PLoS One
Volume 9, Issue 12, Pages e113800
出版商
Public Library of Science (PLoS)
发表日期
2014-12-13
DOI
10.1371/journal.pone.0113800
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。- Meander: visually exploring the structural variome using space-filling curves
- (2013) G. A. Pavlopoulos et al. NUCLEIC ACIDS RESEARCH
- The Database of Genomic Variants: a curated collection of structural variation in the human genome
- (2013) Jeffrey R. MacDonald et al. NUCLEIC ACIDS RESEARCH
- Comparative Studies of Copy Number Variation Detection Methods for Next-Generation Sequencing Technologies
- (2013) Junbo Duan et al. PLoS One
- LNCipedia: a database for annotated human lncRNA transcript sequences and structures
- (2012) Pieter-Jan Volders et al. NUCLEIC ACIDS RESEARCH
- Constitutional Chromothripsis Rearrangements Involve Clustered Double-Stranded DNA Breaks and Nonhomologous Repair Mechanisms
- (2012) Wigard P. Kloosterman et al. Cell Reports
- Next-Generation Sequencing Strategies Enable Routine Detection of Balanced Chromosome Rearrangements for Clinical Diagnostics and Genetic Research
- (2011) Michael E. Talkowski et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Fast and accurate long-read alignment with Burrows–Wheeler transform
- (2010) Heng Li et al. BIOINFORMATICS
- Stampy: A statistical algorithm for sensitive and fast mapping of Illumina sequence reads
- (2010) G. Lunter 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
- Gremlin: An Interactive Visualization Model for Analyzing Genomic Rearrangements
- (2010) T M O'Brien et al. IEEE TRANSACTIONS ON VISUALIZATION AND COMPUTER GRAPHICS
- The UCSC Genome Browser database: update 2011
- (2010) P. A. Fujita et al. NUCLEIC ACIDS RESEARCH
- Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads
- (2009) K. Ye 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
- CNV-seq, a new method to detect copy number variation using high-throughput sequencing
- (2009) Chao Xie et al. BMC BIOINFORMATICS
- Computational methods for discovering structural variation with next-generation sequencing
- (2009) Paul Medvedev et al. NATURE METHODS
- BreakDancer: an algorithm for high-resolution mapping of genomic structural variation
- (2009) Ken Chen et al. NATURE METHODS
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
- (2009) Ben Langmead et al. GENOME BIOLOGY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk 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