Meraculous: De Novo Genome Assembly with Short Paired-End Reads
JA Chapman, I Ho, S Sunkara, S Luo, GP Schroth… - PloS one, 2011 - journals.plos.org
We describe a new algorithm, meraculous, for whole genome assembly of deep paired-end
short reads, and apply it to the assembly of a dataset of paired 75-bp Illumina reads derived …
short reads, and apply it to the assembly of a dataset of paired 75-bp Illumina reads derived …
De novo genome assembly: what every biologist should know
M Baker - Nature methods, 2012 - nature.com
Asked how mature the field of genome assembly is, Ian Korf at the University of California,
Davis, compares it to a teenager with great capabilities.“It's got bold assertions about what it …
Davis, compares it to a teenager with great capabilities.“It's got bold assertions about what it …
Efficient de novo assembly of highly heterozygous genomes from whole-genome shotgun short reads
R Kajitani, K Toshimoto, H Noguchi, A Toyoda… - Genome …, 2014 - genome.cshlp.org
Although many de novo genome assembly projects have recently been conducted using
high-throughput sequencers, assembling highly heterozygous diploid genomes is a …
high-throughput sequencers, assembling highly heterozygous diploid genomes is a …
Long road to long-read assembly
V Marx - Nature Methods, 2021 - nature.com
Long road to long-read assembly | Nature Methods Skip to main content Thank you for
visiting nature.com. You are using a browser version with limited support for CSS. To obtain …
visiting nature.com. You are using a browser version with limited support for CSS. To obtain …
Contiguous and accurate de novo assembly of metazoan genomes with modest long read coverage
M Chakraborty, JG Baldwin-Brown… - Nucleic acids …, 2016 - academic.oup.com
Genome assemblies that are accurate, complete and contiguous are essential for identifying
important structural and functional elements of genomes and for identifying genetic variation …
important structural and functional elements of genomes and for identifying genetic variation …
DBG2OLC: efficient assembly of large genomes using long erroneous reads of the third generation sequencing technologies
The highly anticipated transition from next generation sequencing (NGS) to third generation
sequencing (3GS) has been difficult primarily due to high error rates and excessive …
sequencing (3GS) has been difficult primarily due to high error rates and excessive …
Assembly of large genomes using second-generation sequencing
MC Schatz, AL Delcher, SL Salzberg - Genome research, 2010 - genome.cshlp.org
Second-generation sequencing technology can now be used to sequence an entire human
genome in a matter of days and at low cost. Sequence read lengths, initially very short, have …
genome in a matter of days and at low cost. Sequence read lengths, initially very short, have …
The present and future of de novo whole-genome assembly
As the advent of next-generation sequencing (NGS) technology, various de novo assembly
algorithms based on the de Bruijn graph have been developed to construct chromosome …
algorithms based on the de Bruijn graph have been developed to construct chromosome …
Assemblathon 1: a competitive assessment of de novo short read assembly methods
Low-cost short read sequencing technology has revolutionized genomics, though it is only
just becoming practical for the high-quality de novo assembly of a novel large genome. We …
just becoming practical for the high-quality de novo assembly of a novel large genome. We …