We demonstrate that genome sequences approaching finished quality can be generated from short paired reads. Using 36 base (fragment) and 26 base (jumping) reads from five microbial genomes of varied GC composition and sizes up to 40 Mb, ALLPATHS2 generated assemblies with long, accurate contigs and scaffolds. Velvet and EULER-SR were less accurate. For example, for Escherichia coli, the fraction of 10-kb stretches that were perfect was 99.8% (ALLPATHS2), 68.7% (Velvet), and 42.1% (EULER-SR).Organismic and Evolutionary Biolog
De novo Genome assembly and k-mer frequency counting are two of the classical prob- lems of Bioinfo...
International audienceNext-generation sequencing technology is enabling massive production of high-q...
Genomic research relies on computers to process large amounts of genomic data. In order to digitize ...
New DNA sequencing technologies deliver data at dramatically lower costs but demand new analytical m...
One of the most significant advances in biology has been the ability to sequence the DNA of organism...
Advances in sequencing technology allow genomes to be sequenced at vastly decreased costs. However, ...
Motivation: Paired-end sequencing allows circumventing the shortness of the reads produced by second...
BACKGROUND: Long-read and short-read sequencing technologies offer competing advantages for eukaryot...
New sequencing technology has dramatically altered the landscape of whole-genome sequencing, allowin...
A genome sequence assembly provides the foundation for studies of genotypic and phenotypic variation...
Single-molecule sequencing instruments can generate multikilobase sequences with the potential to gr...
Background: De Bruijn graphs are a theoretical framework underlying several modern genome assembly p...
Background: Short read DNA sequencing technologies have revolutionized genome assembly by providing ...
Recently news technologies in molecular biology enormously improved the sequencing data production, ...
Genome assembly is a critical first step for biological discovery. All current sequencing technologi...
De novo Genome assembly and k-mer frequency counting are two of the classical prob- lems of Bioinfo...
International audienceNext-generation sequencing technology is enabling massive production of high-q...
Genomic research relies on computers to process large amounts of genomic data. In order to digitize ...
New DNA sequencing technologies deliver data at dramatically lower costs but demand new analytical m...
One of the most significant advances in biology has been the ability to sequence the DNA of organism...
Advances in sequencing technology allow genomes to be sequenced at vastly decreased costs. However, ...
Motivation: Paired-end sequencing allows circumventing the shortness of the reads produced by second...
BACKGROUND: Long-read and short-read sequencing technologies offer competing advantages for eukaryot...
New sequencing technology has dramatically altered the landscape of whole-genome sequencing, allowin...
A genome sequence assembly provides the foundation for studies of genotypic and phenotypic variation...
Single-molecule sequencing instruments can generate multikilobase sequences with the potential to gr...
Background: De Bruijn graphs are a theoretical framework underlying several modern genome assembly p...
Background: Short read DNA sequencing technologies have revolutionized genome assembly by providing ...
Recently news technologies in molecular biology enormously improved the sequencing data production, ...
Genome assembly is a critical first step for biological discovery. All current sequencing technologi...
De novo Genome assembly and k-mer frequency counting are two of the classical prob- lems of Bioinfo...
International audienceNext-generation sequencing technology is enabling massive production of high-q...
Genomic research relies on computers to process large amounts of genomic data. In order to digitize ...