[HTML][HTML] Assembly algorithms for next-generation sequencing data

JR Miller, S Koren, G Sutton - Genomics, 2010 - Elsevier
The emergence of next-generation sequencing platforms led to resurgence of research in
whole-genome shotgun assembly algorithms and software. DNA sequencing data from the …

A primer on metagenomics

JC Wooley, A Godzik, I Friedberg - PLoS computational biology, 2010 - journals.plos.org
Metagenomics is a discipline that enables the genomic study of uncultured microorganisms.
Faster, cheaper sequencing technologies and the ability to sequence uncultured microbes …

GenASM: A high-performance, low-power approximate string matching acceleration framework for genome sequence analysis

DS Cali, GS Kalsi, Z Bingöl, C Firtina… - 2020 53rd Annual …, 2020 - ieeexplore.ieee.org
Genome sequence analysis has enabled significant advancements in medical and scientific
areas such as personalized medicine, outbreak tracing, and the understanding of evolution …

LoRDEC: accurate and efficient long read error correction

L Salmela, E Rivals - Bioinformatics, 2014 - academic.oup.com
Motivation: PacBio single molecule real-time sequencing is a third-generation sequencing
technique producing long reads, with comparatively lower throughput and higher error rate …

Genome sequence and analysis of the tuber crop potato

X Xu, P Pan, S Cheng, B Zhang, D Mu, P Ni, G Zhang… - 2011 - cgspace.cgiar.org
Potato (Solanum tuberosum L.) is the world's most important non-grain food crop and is
central to global food security. It is clonally propagated, highly heterozygous, autotetraploid …

Velvet: algorithms for de novo short read assembly using de Bruijn graphs

DR Zerbino, E Birney - Genome research, 2008 - genome.cshlp.org
We have developed a new set of algorithms, collectively called “Velvet,” to manipulate de
Bruijn graphs for genomic sequence assembly. A de Bruijn graph is a compact …

Denoising DNA deep sequencing data—high-throughput sequencing errors and their correction

D Laehnemann, A Borkhardt… - Briefings in …, 2016 - academic.oup.com
Characterizing the errors generated by common high-throughput sequencing platforms and
telling true genetic variation from technical artefacts are two interdependent steps, essential …

[HTML][HTML] Ray: simultaneous assembly of reads from a mix of high-throughput sequencing technologies

S Boisvert, F Laviolette, J Corbeil - 2010 - liebertpub.com
An accurate genome sequence of a desired species is now a pre-requisite for genome
research. An important step in obtaining a high-quality genome sequence is to correctly …

Emerging technologies in DNA sequencing

ML Metzker - Genome research, 2005 - genome.cshlp.org
Demand for DNA sequence information has never been greater, yet current Sanger
technology is too costly, time consuming, and labor intensive to meet this ongoing demand …

Lighter: fast and memory-efficient sequencing error correction without counting

L Song, L Florea, B Langmead - Genome biology, 2014 - Springer
Lighter is a fast, memory-efficient tool for correcting sequencing errors. Lighter avoids
counting k-mers. Instead, it uses a pair of Bloom filters, one holding a sample of the input k …