High throughput sequencing (HTS) platforms generate unprecedented amounts of data that introduce challenges for processing and downstream analysis. While tools that report the 'best' mapping location of each read provide a fast way to process HTS data, they are not suitable for many types of downstream analysis such as structural variation detection, where it is important to report multiple mapping loci for each read. For this purpose we introduce mrsFAST-Ultra, a fast, cache oblivious, SNP-aware aligner that can handle the multi-mapping of HTS reads very efficiently. mrsFAST-Ultra improves mrsFAST, our first cache oblivious read aligner capable of handling multi-mapping reads, through new and compact index structures that reduce not only t...
Motivation: Discovering variation among high throughput sequenced genomes relies on efficient and ef...
Motivation: Discovering variation among high-throughput sequenced genomes relies on efficient and ef...
Abstract With the introduction of next-generation sequencing (NGS) technologies, we are facing an ex...
Cataloged from PDF version of article.High throughput sequencing (HTS) platforms generate unpreceden...
The high throughput sequencing (HTS) platforms generate unprecedented amounts of data that introduce...
High throughput sequencing (HTS) platforms gener-ate unprecedented amounts of data that introduce ch...
The high throughput sequencing (HTS) platforms generate unprecedented amounts of data that introduce...
Many recent advances in genomics and the expectations of personalized medicine are made possible tha...
Bowtie is an ultrafast, memory-efficient alignment program for aligning short DNA sequence reads to ...
With the introduction of next-generation sequencing (NGS) technologies, we are facing an exponential...
Abstract Background DNA sequence alignment is a common first step in most applications of high-throu...
Rapidly decreasing genome sequencing costs have led to a proportionate increase in the number of sam...
Motivation: Next-generation DNA sequencing machines are generating an enormous amount of sequence da...
Next generation sequencing has increased the throughput of sequenced DNA into the range of billions ...
The growing volume of generated DNA sequencing data makes the problem of its long-term storage incre...
Motivation: Discovering variation among high throughput sequenced genomes relies on efficient and ef...
Motivation: Discovering variation among high-throughput sequenced genomes relies on efficient and ef...
Abstract With the introduction of next-generation sequencing (NGS) technologies, we are facing an ex...
Cataloged from PDF version of article.High throughput sequencing (HTS) platforms generate unpreceden...
The high throughput sequencing (HTS) platforms generate unprecedented amounts of data that introduce...
High throughput sequencing (HTS) platforms gener-ate unprecedented amounts of data that introduce ch...
The high throughput sequencing (HTS) platforms generate unprecedented amounts of data that introduce...
Many recent advances in genomics and the expectations of personalized medicine are made possible tha...
Bowtie is an ultrafast, memory-efficient alignment program for aligning short DNA sequence reads to ...
With the introduction of next-generation sequencing (NGS) technologies, we are facing an exponential...
Abstract Background DNA sequence alignment is a common first step in most applications of high-throu...
Rapidly decreasing genome sequencing costs have led to a proportionate increase in the number of sam...
Motivation: Next-generation DNA sequencing machines are generating an enormous amount of sequence da...
Next generation sequencing has increased the throughput of sequenced DNA into the range of billions ...
The growing volume of generated DNA sequencing data makes the problem of its long-term storage incre...
Motivation: Discovering variation among high throughput sequenced genomes relies on efficient and ef...
Motivation: Discovering variation among high-throughput sequenced genomes relies on efficient and ef...
Abstract With the introduction of next-generation sequencing (NGS) technologies, we are facing an ex...