We present a parallel algorithm and scalable implementation for genome analysis, specifically the problem of finding overlaps and alignments for data from "third generation" long read sequencers [29]. While long sequences of DNA offer enormous advantages for biological analysis and insight, current long read sequencing instruments have high error rates and therefore require different approaches to analysis than their short read counterparts. Our work focuses on an efficient distributed-memory parallelization of an accurate single-node algorithm for overlapping and aligning long reads. We achieve scalability of this irregular algorithm by addressing the competing issues of increasing parallelism, minimizing communication, constraining the me...
With growing throughput and dropping cost of High-Throughput Sequencing (HTS) technologies, there is...
Ultrascale computing and bioinformatics are two rapidly growing fields with a big impact right now a...
Motivation: Many programs for aligning short sequencing reads to a reference genome have been develo...
The challenge of comparing two or more genomes that have undergone recombination and substantial amo...
Alignment of long DNA sequences is a challenging task due to its high demands for computational powe...
Distributed Shared Memory systems allow the use of the shared memory programming paradigm in distrib...
Distributed Shared Memory systems allow the use of the shared memory programming paradigm in distrib...
Genomic sequence alignment is an important technique to decode genome sequences in bioinformatics. N...
The genome sequence alignment problems are very important ones from the computational biology perspe...
Third generation sequencing machines produce reads with tens of thousands of base pairs.To perform d...
With the advent of High performance computing, it is now possible to achieve orders of magnitude per...
Aligning a set of query sequences to a set of target sequences is an important task in bioinformatic...
One of the most computationally intensive tasks in computational biology is de novo genome assembly,...
The growth of next-generation sequencing (NGS) datasets poses a challenge to the align-ment of reads...
Aligning sequencing reads onto a reference is an essential step of the majority of genomic analysis ...
With growing throughput and dropping cost of High-Throughput Sequencing (HTS) technologies, there is...
Ultrascale computing and bioinformatics are two rapidly growing fields with a big impact right now a...
Motivation: Many programs for aligning short sequencing reads to a reference genome have been develo...
The challenge of comparing two or more genomes that have undergone recombination and substantial amo...
Alignment of long DNA sequences is a challenging task due to its high demands for computational powe...
Distributed Shared Memory systems allow the use of the shared memory programming paradigm in distrib...
Distributed Shared Memory systems allow the use of the shared memory programming paradigm in distrib...
Genomic sequence alignment is an important technique to decode genome sequences in bioinformatics. N...
The genome sequence alignment problems are very important ones from the computational biology perspe...
Third generation sequencing machines produce reads with tens of thousands of base pairs.To perform d...
With the advent of High performance computing, it is now possible to achieve orders of magnitude per...
Aligning a set of query sequences to a set of target sequences is an important task in bioinformatic...
One of the most computationally intensive tasks in computational biology is de novo genome assembly,...
The growth of next-generation sequencing (NGS) datasets poses a challenge to the align-ment of reads...
Aligning sequencing reads onto a reference is an essential step of the majority of genomic analysis ...
With growing throughput and dropping cost of High-Throughput Sequencing (HTS) technologies, there is...
Ultrascale computing and bioinformatics are two rapidly growing fields with a big impact right now a...
Motivation: Many programs for aligning short sequencing reads to a reference genome have been develo...