Motivation: The boost of next-generation sequencing technologies provides us with an unprecedented opportunity for elucidating genetic mysteries, yet the short-read length hinders us from better assembling the genome from scratch. New protocols now exist that can generate overlapping pair-end reads. By joining the 3â ² ends of each read pair, one is able to construct longer reads for assembling. However, effectively joining two overlapped pair-end reads remains a challenging task.Result: In this article, we present an efficient tool called Connecting Overlapped Pair-End (COPE) reads, to connect overlapping pair-end reads using k-mer frequencies. We evaluated our tool on 30Ã simulated pair-end reads from Arabidopsis thaliana with 1% base er...
Inexpensive de novo genome sequencing, particularly in organisms with small genomes, is now possible...
Abstract Background High throughput sequencing (HTS) platforms produce gigabases of short read (de n...
We describe a new algorithm, meraculous, for whole genome assembly of deep paired-end short reads, a...
Motivation: The boost of next-generation sequencing technologies provides us with an unprecedented o...
De novo Genome assembly and k-mer frequency counting are two of the classical prob- lems of Bioinfo...
MotivationDe novo assemblies of genomes remain one of the most challenging applications in next-gene...
We present a reliable, easy to implement algorithm to generate a set of highly reliable overlaps bas...
. These authors contributed equally to this work. Since the read lengths of high throughput sequenci...
Abstract Background Short read DNA sequencing technologies have revolutionized genome assembly by pr...
Motivation: DNA sequence reads from Sanger and pyrosequencing platforms differ in cost, accuracy, ty...
We present a reliable, easy to implement algorithm to generate a set of highly reliable overlaps bas...
We describe a new algorithm, meraculous, for whole genome assembly of deep paired-end short reads, a...
We describe a new algorithm, meraculous, for whole genome assembly of deep paired-end short reads, a...
Paired-end sequencing allows circumventing the shortness of the reads produced by second generation ...
Genome sequence assembly presents a fascinating and frequently-changing challenge. As DNA sequencing...
Inexpensive de novo genome sequencing, particularly in organisms with small genomes, is now possible...
Abstract Background High throughput sequencing (HTS) platforms produce gigabases of short read (de n...
We describe a new algorithm, meraculous, for whole genome assembly of deep paired-end short reads, a...
Motivation: The boost of next-generation sequencing technologies provides us with an unprecedented o...
De novo Genome assembly and k-mer frequency counting are two of the classical prob- lems of Bioinfo...
MotivationDe novo assemblies of genomes remain one of the most challenging applications in next-gene...
We present a reliable, easy to implement algorithm to generate a set of highly reliable overlaps bas...
. These authors contributed equally to this work. Since the read lengths of high throughput sequenci...
Abstract Background Short read DNA sequencing technologies have revolutionized genome assembly by pr...
Motivation: DNA sequence reads from Sanger and pyrosequencing platforms differ in cost, accuracy, ty...
We present a reliable, easy to implement algorithm to generate a set of highly reliable overlaps bas...
We describe a new algorithm, meraculous, for whole genome assembly of deep paired-end short reads, a...
We describe a new algorithm, meraculous, for whole genome assembly of deep paired-end short reads, a...
Paired-end sequencing allows circumventing the shortness of the reads produced by second generation ...
Genome sequence assembly presents a fascinating and frequently-changing challenge. As DNA sequencing...
Inexpensive de novo genome sequencing, particularly in organisms with small genomes, is now possible...
Abstract Background High throughput sequencing (HTS) platforms produce gigabases of short read (de n...
We describe a new algorithm, meraculous, for whole genome assembly of deep paired-end short reads, a...