In the assembly pipeline of Whole Genome Sequencing (WGS), read mapping is a widely used method to re-assemble the genome. It employs approximate string matching and dynamic programming-based algorithms on a large volume of data and associated structures, making it a computationally intensive process. Currently, the state-of-the-art data centers for genome sequencing incur substantial setup and energy costs for maintaining hardware, data storage and cooling systems. To enable low-cost genomics, we propose an energy-efficient architectural methodology for read mapping using a single system-on-chip (SoC) platform. The proposed methodology is based on the q-gram lemma and designed using a novel architecture for filtering and verification. The ...
The alignment of short DNA read sequencing data to a human reference genome sequence has become a st...
Thesis (Ph.D.)--University of Washington, 2018Advances in next-generation sequencing technology have...
Summarization: The ever-increasing genomic dataset sizes, fueled by continuous advances in DNA seque...
In the assembly pipeline of Whole Genome Sequencing (WGS), read mapping is a widely used method to r...
Genomics is transforming medicine from reactive to personalized, predictive, preventive and particip...
© 2019 IEEE. Read mapping is a process in which DNA reads are mapped to a reference genome through f...
With over 6000 known genetic disorders, genomics is a key driver to transform the current generation...
Bioinformatics is one of the emerging trends in today’s world. The major part of bioinformatics is d...
Genome assemblies sequenced by a Whole Genome Shotgun (WGS) project predict an organism’s fun...
Abstract—In bioinformatics, short read alignment is a computationally intensive operation that invol...
Genome sequence analysis is central to today’s genomics research, and sequence alignment and Single-...
The analysis of next-generation sequencing (NGS) data is a major topic in bioinfor-matics: short rea...
Genome analysis benefits precise medical care, wildlife conservation, pandemic treatment, e.g., COVI...
High throughput DNA sequencing made individual genome profiling possible and produces very large amo...
String matching is the searching of patterns in a very long string called text. It is involved in DN...
The alignment of short DNA read sequencing data to a human reference genome sequence has become a st...
Thesis (Ph.D.)--University of Washington, 2018Advances in next-generation sequencing technology have...
Summarization: The ever-increasing genomic dataset sizes, fueled by continuous advances in DNA seque...
In the assembly pipeline of Whole Genome Sequencing (WGS), read mapping is a widely used method to r...
Genomics is transforming medicine from reactive to personalized, predictive, preventive and particip...
© 2019 IEEE. Read mapping is a process in which DNA reads are mapped to a reference genome through f...
With over 6000 known genetic disorders, genomics is a key driver to transform the current generation...
Bioinformatics is one of the emerging trends in today’s world. The major part of bioinformatics is d...
Genome assemblies sequenced by a Whole Genome Shotgun (WGS) project predict an organism’s fun...
Abstract—In bioinformatics, short read alignment is a computationally intensive operation that invol...
Genome sequence analysis is central to today’s genomics research, and sequence alignment and Single-...
The analysis of next-generation sequencing (NGS) data is a major topic in bioinfor-matics: short rea...
Genome analysis benefits precise medical care, wildlife conservation, pandemic treatment, e.g., COVI...
High throughput DNA sequencing made individual genome profiling possible and produces very large amo...
String matching is the searching of patterns in a very long string called text. It is involved in DN...
The alignment of short DNA read sequencing data to a human reference genome sequence has become a st...
Thesis (Ph.D.)--University of Washington, 2018Advances in next-generation sequencing technology have...
Summarization: The ever-increasing genomic dataset sizes, fueled by continuous advances in DNA seque...