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High Performance and Scalable Matching and Assembly of Biological Sequences
Abu Doleh, Anas

2016, Doctor of Philosophy, Ohio State University, Electrical and Computer Engineering.
Next Generation Sequencing (NGS), the massive parallel and low-cost sequencing
technology, is able to generate an enormous size of sequencing data. This facilitates
the discovery of new genomic sequences and expands the biological and medical
research. However, these big advancements in this technology also bring big computational
challenges. In almost all NGS analysis pipelines, the most crucial and computationally
intensive tasks are sequence similarity searching and de novo genome assembly. Thus, in this
work, we introduced novel and efficient techniques to utilize the advancements in the
High Performance Computing hardware and data computing platforms in order to
accelerate these tasks while producing high quality results.

For the sequence similarity search, we have studied utilizing the massively multithreaded
architectures, such as Graphical Processing Unit (GPU), in accelerating and solving
two important problems: reads mapping and maximal exact matching. Firstly, we introduced
a new mapping tool, Masher, which processes long~(and short) reads efficiently and
accurately. Masher employs a novel indexing technique that produces an index for
huge genome, such as the human genome, with a small memory footprint such that
it could be stored and efficiently accessed in a restricted-memory device such as a GPU.
The results show that Masher is faster than state-of-the-art tools and obtains a good
accuracy and sensitivity on sequencing data with various characteristics. Secondly,
maximal exact matching problem has been studied because of its importance in
detection and evaluating the similarity between sequences. We introduced a novel
tool, GPUMEM, which efficiently utilizes GPU in building a lightweight indexing and
finding maximal exact matches inside two genome sequences. The index construction
is so fast that even by including its time, GPUMEM is faster in practice than state-of-the-art
tools that use a pre-built index.

De novo genome assembly is a crucial step in NGS analysis because of the novelty of
discovered sequences. Firstly, we have studied parallelizing the de Bruijn graph based
de novo genome assembly on distributed memory systems using Spark framework and
GraphX API. We proposed a new tool, Spaler, which assembles short reads efficiently
and accurately. Spaler starts with the de Bruijn graph construction. Then, it applies an iterative
graph reduction and simplification techniques to generate contigs. After that, Spaler uses
the reads mapping information to produce scaffolds. Spaler employs smart parallelism
level tuning technique to improve the performance in each of these steps independently.
The experiments show promising results in term of scalability, execution time and quality.
Secondly, we addressed the problem of de novo metagenomics assembly. Spaler may
not properly assemble the sequenced data extracted from environmental samples.
This is because of the complexity and diversity of the living microbial communities.
Thus, we introduced meta-Spaler, an extension of Spaler, to handle metagenomics
dataset. meta-Spaler partitions the reads based on their expected coverage and applies
an iterative assembly. The results show an improving in the assembly quality of meta-Spaler
in comparison to the assembly of Spaler.
Umit Catalyurek (Advisor)
Kun Huang (Committee Member)
Fusun Ozguner (Committee Member)
157 p.

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Abu Doleh, Anas "High Performance and Scalable Matching and Assembly of Biological Sequences." Electronic Thesis or Dissertation. Ohio State University, 2016. https://etd.ohiolink.edu/

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