With the advent of several accurate and sophisticated statistical algorithms and pipelines for DNA sequence analysis, it is becoming increasingly possible to translate raw sequencing data into biologically meaningful information for further clinical analysis and processing. However, given the large volume of the data involved, even modestly complex algorithms would require a prohibitively long time to complete. Hence it is urgent to explore non-conventional implementation platforms to accelerate genomics research. In this thesis, we present a Field-Programmable Gate Array (FPGA) accelerated implementation of the Pair Hidden Markov Model (Pair HMM) forward algorithm, the performance bottleneck in the HaplotypeCaller, a critical function ...
International audienceWe propose a new parallelization scheme for the hmmsearch function of the HMME...
Recent advances in DNA sequencing technology have opened new doors for scientists to use genomic dat...
We now need more than ever to make genome analysis more intelligent. We need to read, analyze, and i...
With the advent of several accurate and sophisticated statistical algorithms and pipelines for DNA s...
Next generation sequencing (NGS) technologies have transformed the landscape of genomic research. Wi...
With the rise of Next-Generation Sequencing (NGS), clinical sequencing services have become more acc...
GATK HaplotypeCaller (HC) is a popular variant caller, which is widely used to identify variants in ...
GATK HaplotypeCaller (HC) is a popular variant caller, which is widely used to identify variants in ...
DNA carries all the information needed to define the genetic structure of an individual. The large a...
In order to handle the massive raw data generated by next generation sequencing (NGS) platforms, GPU...
In order to handle the massive raw data generated by next generation sequencing (NGS) platforms, GPU...
The hidden Markov model, known as HMM, is an important type of statistical model with extensive app...
International audienceWe propose a new parallelization scheme for the hmmsearch function of the HMME...
International audienceWe propose a new parallelization scheme for the hmmsearch function of the HMME...
International audienceWe propose a new parallelization scheme for the hmmsearch function of the HMME...
International audienceWe propose a new parallelization scheme for the hmmsearch function of the HMME...
Recent advances in DNA sequencing technology have opened new doors for scientists to use genomic dat...
We now need more than ever to make genome analysis more intelligent. We need to read, analyze, and i...
With the advent of several accurate and sophisticated statistical algorithms and pipelines for DNA s...
Next generation sequencing (NGS) technologies have transformed the landscape of genomic research. Wi...
With the rise of Next-Generation Sequencing (NGS), clinical sequencing services have become more acc...
GATK HaplotypeCaller (HC) is a popular variant caller, which is widely used to identify variants in ...
GATK HaplotypeCaller (HC) is a popular variant caller, which is widely used to identify variants in ...
DNA carries all the information needed to define the genetic structure of an individual. The large a...
In order to handle the massive raw data generated by next generation sequencing (NGS) platforms, GPU...
In order to handle the massive raw data generated by next generation sequencing (NGS) platforms, GPU...
The hidden Markov model, known as HMM, is an important type of statistical model with extensive app...
International audienceWe propose a new parallelization scheme for the hmmsearch function of the HMME...
International audienceWe propose a new parallelization scheme for the hmmsearch function of the HMME...
International audienceWe propose a new parallelization scheme for the hmmsearch function of the HMME...
International audienceWe propose a new parallelization scheme for the hmmsearch function of the HMME...
Recent advances in DNA sequencing technology have opened new doors for scientists to use genomic dat...
We now need more than ever to make genome analysis more intelligent. We need to read, analyze, and i...