NGSView: an extensible open source editor for next-generation sequencing data

被引:8
作者
Arner, Erik [1 ]
Hayashizaki, Yoshihide [1 ]
Daub, Carsten O. [1 ]
机构
[1] RIKEN Yokohama Inst, RIKEN Omics Sci Ctr, Tsurumi Ku, Kanagawa 2300045, Japan
关键词
SHORT READS; TECHNOLOGY; ALGORITHMS; GENOMES; TOOL;
D O I
10.1093/bioinformatics/btp611
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
High-throughput sequencing technologies introduce novel demands on tools available for data analysis. We have developed NGSView (Next Generation Sequence View), a generally applicable, flexible and extensible next-generation sequence alignment editor. The software allows for visualization and manipulation of millions of sequences simultaneously on a desktop computer, through a graphical interface. NGSView is available under an open source license and can be extended through a well documented API.
引用
收藏
页码:125 / 126
页数:2
相关论文
共 18 条
[1]   DNPTrapper: an assembly editing tool for finishing and analysis of complex repeat regions [J].
Arner, E ;
Tammi, MT ;
Tran, AN ;
Kindlund, E ;
Andersson, B .
BMC BIOINFORMATICS, 2006, 7 (1)
[2]   MapView: visualization of short reads alignment on a desktop computer [J].
Bao, Hua ;
Guo, Hui ;
Wang, Jinwei ;
Zhou, Renchao ;
Lu, Xuemei ;
Shi, Suhua .
BIOINFORMATICS, 2009, 25 (12) :1554-1555
[3]   FindPeaks 3.1: a tool for identifying areas of enrichment from massively parallel short-read sequencing technology [J].
Fejes, Anthony P. ;
Robertson, Gordon ;
Bilenky, Mikhail ;
Varhol, Richard ;
Bainbridge, Matthew ;
Jones, Steven J. M. .
BIOINFORMATICS, 2008, 24 (15) :1729-1730
[4]   The new paradigm of flow cell sequencing [J].
Holt, Robert A. ;
Jones, Steven J. M. .
GENOME RESEARCH, 2008, 18 (06) :839-846
[5]   Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes [J].
Hormozdiari, Fereydoun ;
Alkan, Can ;
Eichler, Evan E. ;
Sahinalp, S. Cenk .
GENOME RESEARCH, 2009, 19 (07) :1270-1278
[6]   EagleView: A genome assembly viewer for next-generation sequencing technologies [J].
Huang, Weichun ;
Marth, Gabor .
GENOME RESEARCH, 2008, 18 (09) :1538-1543
[7]   High-throughput genotyping by whole-genome resequencing [J].
Huang, Xuehui ;
Feng, Qi ;
Qian, Qian ;
Zhao, Qiang ;
Wang, Lu ;
Wang, Ahong ;
Guan, Jianping ;
Fan, Danlin ;
Weng, Qijun ;
Huang, Tao ;
Dong, Guojun ;
Sang, Tao ;
Han, Bin .
GENOME RESEARCH, 2009, 19 (06) :1068-1076
[8]   Ensembl 2009 [J].
Hubbard, T. J. P. ;
Aken, B. L. ;
Ayling, S. ;
Ballester, B. ;
Beal, K. ;
Bragin, E. ;
Brent, S. ;
Chen, Y. ;
Clapham, P. ;
Clarke, L. ;
Coates, G. ;
Fairley, S. ;
Fitzgerald, S. ;
Fernandez-Banet, J. ;
Gordon, L. ;
Graf, S. ;
Haider, S. ;
Hammond, M. ;
Holland, R. ;
Howe, K. ;
Jenkinson, A. ;
Johnson, N. ;
Kahari, A. ;
Keefe, D. ;
Keenan, S. ;
Kinsella, R. ;
Kokocinski, F. ;
Kulesha, E. ;
Lawson, D. ;
Longden, I. ;
Megy, K. ;
Meidl, P. ;
Overduin, B. ;
Parker, A. ;
Pritchard, B. ;
Rios, D. ;
Schuster, M. ;
Slater, G. ;
Smedley, D. ;
Spooner, W. ;
Spudich, G. ;
Trevanion, S. ;
Vilella, A. ;
Vogel, J. ;
White, S. ;
Wilder, S. ;
Zadissa, A. ;
Birney, E. ;
Cunningham, F. ;
Curwen, V. .
NUCLEIC ACIDS RESEARCH, 2009, 37 :D690-D697
[9]   An integrated software system for analyzing ChIP-chip and ChIP-seq data [J].
Ji, Hongkai ;
Jiang, Hui ;
Ma, Wenxiu ;
Johnson, David S. ;
Myers, Richard M. ;
Wong, Wing H. .
NATURE BIOTECHNOLOGY, 2008, 26 (11) :1293-1300
[10]   PEMer: a computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing data [J].
Korbel, Jan O. ;
Abyzov, Alexej ;
Mu, Xinmeng Jasmine ;
Carriero, Nicholas ;
Cayting, Philip ;
Zhang, Zhengdong ;
Snyder, Michael ;
Gerstein, Mark B. .
GENOME BIOLOGY, 2009, 10 (02)