Abstract Background Although single molecule sequencing is still improving, the lengths of the generated sequences are inevitably an advantage in genome assembly. Prior work that utilizes long reads to conduct genome assembly has mostly focused on correcting sequencing errors and improving contiguity of de novo assemblies. Results We propose a disassembling-reassembling approach for both correcting structural errors in the draft assembly and scaffolding a target assembly based on error-corrected single molecule sequences. To achieve this goal, we formulate a maximum alternating path cover problem. We prove that this problem is NP-hard, and solve it by a 2-approximation algorithm. Conclusions Our experimental results show that our approach c...
© The Author 2017. Published by Oxford University Press. All rights reserved. The application of adv...
Single-molecule sequencing instruments can generate multikilobase sequences with the potential to gr...
Genome assembly is the problem of reconstructing genomes from DNA sequence reads. Even the best asse...
Motivation: The increasing availability of second-generation highthroughput sequencing (HTS) technol...
Not AvailableCurrent de-novo assemblers are unable to effectively use the long-read sequencing data ...
One of the most significant advances in biology has been the ability to sequence the DNA of organism...
Accurate de novo assembly using short reads generated by next generation sequencing technologies is ...
Third generation sequencing technologies provide the opportunity to improve genome assemblies by gen...
Background The use of short reads from High Throughput Sequencing (HTS) techniques is now commonplac...
Abstract Background Genome sequencing yields the sequence of many short snippets of DNA (reads) from...
Advances in DNA sequencing technology over the past decade have increased the volume of raw sequence...
Despite the prodigious throughput of the sequencing instruments currently on the market, the assembl...
Motivation: Next-generation high-throughput sequencing has become a state-of-the-art technique in ge...
Advances in sequencing technology allow genomes to be sequenced at vastly decreased costs. However, ...
A genome sequence assembly provides the foundation for studies of genotypic and phenotypic variation...
© The Author 2017. Published by Oxford University Press. All rights reserved. The application of adv...
Single-molecule sequencing instruments can generate multikilobase sequences with the potential to gr...
Genome assembly is the problem of reconstructing genomes from DNA sequence reads. Even the best asse...
Motivation: The increasing availability of second-generation highthroughput sequencing (HTS) technol...
Not AvailableCurrent de-novo assemblers are unable to effectively use the long-read sequencing data ...
One of the most significant advances in biology has been the ability to sequence the DNA of organism...
Accurate de novo assembly using short reads generated by next generation sequencing technologies is ...
Third generation sequencing technologies provide the opportunity to improve genome assemblies by gen...
Background The use of short reads from High Throughput Sequencing (HTS) techniques is now commonplac...
Abstract Background Genome sequencing yields the sequence of many short snippets of DNA (reads) from...
Advances in DNA sequencing technology over the past decade have increased the volume of raw sequence...
Despite the prodigious throughput of the sequencing instruments currently on the market, the assembl...
Motivation: Next-generation high-throughput sequencing has become a state-of-the-art technique in ge...
Advances in sequencing technology allow genomes to be sequenced at vastly decreased costs. However, ...
A genome sequence assembly provides the foundation for studies of genotypic and phenotypic variation...
© The Author 2017. Published by Oxford University Press. All rights reserved. The application of adv...
Single-molecule sequencing instruments can generate multikilobase sequences with the potential to gr...
Genome assembly is the problem of reconstructing genomes from DNA sequence reads. Even the best asse...