[HTML][HTML] Simplifier: a web tool to eliminate redundant NGS contigs

RTJ Ramos, AR Carneiro, V Azevedo… - …, 2012 - ncbi.nlm.nih.gov
Modern genomic sequencing technologies produce a large amount of data with reduced
cost per base; however, this data consists of short reads. This reduction in the size of the …

[HTML][HTML] Graphical contig analyzer for all sequencing platforms (G4ALL): a new stand-alone tool for finishing and draft generation of bacterial genomes

RTJ Ramos, AR Carneiro, PH Caracciolo… - …, 2013 - ncbi.nlm.nih.gov
Genome assembly has always been complicated due to the inherent difficulties of
sequencing technologies, as well the computational methods used to process sequences …

SHARCGS, a fast and highly accurate short-read assembly algorithm for de novo genomic sequencing

JC Dohm, C Lottaz, T Borodina… - Genome …, 2007 - genome.cshlp.org
The latest revolution in the DNA sequencing field has been brought about by the
development of automated sequencers that are capable of generating giga base pair data …

[HTML][HTML] BASE: a practical de novo assembler for large genomes using long NGS reads

B Liu, CM Liu, D Li, Y Li, HF Ting, SM Yiu, R Luo… - BMC genomics, 2016 - Springer
Background De novo genome assembly using NGS data remains a computation-intensive
task especially for large genomes. In practice, efficiency is often a primary concern and …

Ragout—a reference-assisted assembly tool for bacterial genomes

M Kolmogorov, B Raney, B Paten, S Pham - Bioinformatics, 2014 - academic.oup.com
Bacterial genomes are simpler than mammalian ones, and yet assembling the former from
the data currently generated by high-throughput short-read sequencing machines still …

[HTML][HTML] A new strategy for better genome assembly from very short reads

Y Ji, Y Shi, G Ding, Y Li - BMC bioinformatics, 2011 - Springer
Background With the rapid development of the next generation sequencing (NGS)
technology, large quantities of genome sequencing data have been generated. Because of …

Mapsembler, targeted assembly of larges genomes on a desktop computer

P Peterlongo, R Chikhi - 2011 - inria.hal.science
Background: The analysis of next-generation sequencing data from large genomes is a
timely research topic. Sequencers are producing billions of short sequence fragments from …

[HTML][HTML] Combining de novo and reference-guided assembly with scaffold_builder

GGZ Silva, BE Dutilh, TD Matthews, K Elkins… - Source code for biology …, 2013 - Springer
Genome sequencing has become routine, however genome assembly still remains a
challenge despite the computational advances in the last decade. In particular, the …

Comparative genome assembly

M Pop, A Phillippy, AL Delcher… - Briefings in …, 2004 - academic.oup.com
One of the most complex and computationally intensive tasks of genome sequence analysis
is genome assembly. Even today, few centres have the resources, in both software and …

SEQuel: improving the accuracy of genome assemblies

R Ronen, C Boucher, H Chitsaz, P Pevzner - Bioinformatics, 2012 - academic.oup.com
Motivation: Assemblies of next-generation sequencing (NGS) data, although accurate, still
contain a substantial number of errors that need to be corrected after the assembly process …