scholarly journals Subset selection of high-depth next generation sequencing reads for de novo genome assembly using MapReduce framework

BMC Genomics ◽  
2015 ◽  
Vol 16 (Suppl 12) ◽  
pp. S9 ◽  
Author(s):  
Chih-Hao Fang ◽  
Yu-Jung Chang ◽  
Wei-Chun Chung ◽  
Ping-Heng Hsieh ◽  
Chung-Yen Lin ◽  
...  
PLoS ONE ◽  
2013 ◽  
Vol 8 (4) ◽  
pp. e62856 ◽  
Author(s):  
Yen-Chun Chen ◽  
Tsunglin Liu ◽  
Chun-Hui Yu ◽  
Tzen-Yuh Chiang ◽  
Chi-Chuan Hwang

2015 ◽  
Vol 08 (05) ◽  
pp. 1530001 ◽  
Author(s):  
Sonia Farhana Nimmy ◽  
M. S. Kamal

The next generation sequencing (NGS) is an important process which assures inexpensive organization of vast size of raw sequence dataset over any traditional sequencing systems or methods. Various aspects of NGS such as template preparation, sequencing imaging and genome alignment and assembly outline the genome sequencing and alignment. Consequently, de Bruijn graph (dBG) is an important mathematical tool that graphically analyzes how the orientations are constructed in groups of nucleotides. Basically, dBG describes the formation of the genome segments in circular iterative fashions. Some pivotal dBG-based de novo algorithms and software packages such as T-IDBA, Oases, IDBA-tran, Euler, Velvet, ABySS, AllPaths, SOAPde novo and SOAPde novo2 are illustrated in this paper. Consequently, overlap layout consensus (OLC) graph-based algorithms also play vital role in NGS assembly. Some important OLC-based algorithms such as MIRA3, CABOG, Newbler, Edena, Mosaik and SHORTY are portrayed in this paper. It has been experimented that greedy graph-based algorithms and software packages are also vital for proper genome dataset assembly. A few algorithms named SSAKE, SHARCGS and VCAKE help to perform proper genome sequencing.


Diagnostics ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 962
Author(s):  
Dario de Biase ◽  
Matteo Fassan ◽  
Umberto Malapelle

Next-Generation Sequencing (NGS) allows for the sequencing of multiple genes at a very high depth of coverage [...]


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