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You searched for subject:(Massively parallel). Showing records 1 – 30 of 75 total matches.

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University of Rochester

1. Shastri, Lokendra. Evidential reasoning in semantic networks : a formal theory and its parallel implementation.

Degree: PhD, 2009, University of Rochester

 The problem of representing and utilizing a large body of knowledge is fundamental to artificial intelligence. This thesis focuses on two important issues related to… (more)

Subjects/Keywords: Uncertainty; Connectionist; Massively parallel; Incomplete

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APA (6th Edition):

Shastri, L. (2009). Evidential reasoning in semantic networks : a formal theory and its parallel implementation. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/7400

Chicago Manual of Style (16th Edition):

Shastri, Lokendra. “Evidential reasoning in semantic networks : a formal theory and its parallel implementation.” 2009. Doctoral Dissertation, University of Rochester. Accessed July 07, 2020. http://hdl.handle.net/1802/7400.

MLA Handbook (7th Edition):

Shastri, Lokendra. “Evidential reasoning in semantic networks : a formal theory and its parallel implementation.” 2009. Web. 07 Jul 2020.

Vancouver:

Shastri L. Evidential reasoning in semantic networks : a formal theory and its parallel implementation. [Internet] [Doctoral dissertation]. University of Rochester; 2009. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1802/7400.

Council of Science Editors:

Shastri L. Evidential reasoning in semantic networks : a formal theory and its parallel implementation. [Doctoral Dissertation]. University of Rochester; 2009. Available from: http://hdl.handle.net/1802/7400


University of Leicester

2. Huszar, Tunde I. Massively parallel sequencing of forensic markers : sequence variation and forensic application.

Degree: PhD, 2020, University of Leicester

 DNA analyses have been used to aid forensic investigations since 1985 and to date, human identification relies on the typing of polymorphic autosomal short tandem… (more)

Subjects/Keywords: Thesis; Massively Parallel Sequencing; Forensic Markers; Genetics

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APA (6th Edition):

Huszar, T. I. (2020). Massively parallel sequencing of forensic markers : sequence variation and forensic application. (Doctoral Dissertation). University of Leicester. Retrieved from https://doi.org/10.25392/leicester.data.11914548.v1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.803708

Chicago Manual of Style (16th Edition):

Huszar, Tunde I. “Massively parallel sequencing of forensic markers : sequence variation and forensic application.” 2020. Doctoral Dissertation, University of Leicester. Accessed July 07, 2020. https://doi.org/10.25392/leicester.data.11914548.v1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.803708.

MLA Handbook (7th Edition):

Huszar, Tunde I. “Massively parallel sequencing of forensic markers : sequence variation and forensic application.” 2020. Web. 07 Jul 2020.

Vancouver:

Huszar TI. Massively parallel sequencing of forensic markers : sequence variation and forensic application. [Internet] [Doctoral dissertation]. University of Leicester; 2020. [cited 2020 Jul 07]. Available from: https://doi.org/10.25392/leicester.data.11914548.v1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.803708.

Council of Science Editors:

Huszar TI. Massively parallel sequencing of forensic markers : sequence variation and forensic application. [Doctoral Dissertation]. University of Leicester; 2020. Available from: https://doi.org/10.25392/leicester.data.11914548.v1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.803708


University of Illinois – Urbana-Champaign

3. Gahvari, Hormozd. Improving the performance and scalability of algebraic multigrid solvers through applied performance modeling.

Degree: PhD, 0112, 2014, University of Illinois – Urbana-Champaign

 With single-core speeds no longer rising, dramatically increased parallelism is now the means of getting more performance from supercomputers. The current generation of algorithms run… (more)

Subjects/Keywords: Algebraic Multigrid; Performance Modeling; Massively Parallel Architectures

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APA (6th Edition):

Gahvari, H. (2014). Improving the performance and scalability of algebraic multigrid solvers through applied performance modeling. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/50516

Chicago Manual of Style (16th Edition):

Gahvari, Hormozd. “Improving the performance and scalability of algebraic multigrid solvers through applied performance modeling.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 07, 2020. http://hdl.handle.net/2142/50516.

MLA Handbook (7th Edition):

Gahvari, Hormozd. “Improving the performance and scalability of algebraic multigrid solvers through applied performance modeling.” 2014. Web. 07 Jul 2020.

Vancouver:

Gahvari H. Improving the performance and scalability of algebraic multigrid solvers through applied performance modeling. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/2142/50516.

Council of Science Editors:

Gahvari H. Improving the performance and scalability of algebraic multigrid solvers through applied performance modeling. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/50516


University of Melbourne

4. Thirukeswaran, Shalini. Determining the genetic basis of mitochondrial complex I deficiency in children using massively parallel sequencing.

Degree: 2019, University of Melbourne

 Mitochondrial oxidative phosphorylation (OXPHOS) disorders constitute the largest group of inborn errors of metabolism. Complex I (CI) deficiency is the most common enzymatic defect identified… (more)

Subjects/Keywords: mitochondrial disease; complex I; massively parallel sequencing

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APA (6th Edition):

Thirukeswaran, S. (2019). Determining the genetic basis of mitochondrial complex I deficiency in children using massively parallel sequencing. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/225852

Chicago Manual of Style (16th Edition):

Thirukeswaran, Shalini. “Determining the genetic basis of mitochondrial complex I deficiency in children using massively parallel sequencing.” 2019. Doctoral Dissertation, University of Melbourne. Accessed July 07, 2020. http://hdl.handle.net/11343/225852.

MLA Handbook (7th Edition):

Thirukeswaran, Shalini. “Determining the genetic basis of mitochondrial complex I deficiency in children using massively parallel sequencing.” 2019. Web. 07 Jul 2020.

Vancouver:

Thirukeswaran S. Determining the genetic basis of mitochondrial complex I deficiency in children using massively parallel sequencing. [Internet] [Doctoral dissertation]. University of Melbourne; 2019. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/11343/225852.

Council of Science Editors:

Thirukeswaran S. Determining the genetic basis of mitochondrial complex I deficiency in children using massively parallel sequencing. [Doctoral Dissertation]. University of Melbourne; 2019. Available from: http://hdl.handle.net/11343/225852


University of Melbourne

5. Lake, Nicole Janet. Using massively parallel sequencing to determine the genetic basis of Leigh Syndrome, the most common mitochondrial disorder affecting children.

Degree: 2018, University of Melbourne

 Mitochondrial diseases are debilitating illnesses caused by mutations that impair mitochondrial energy generation. The most common clinical presentation of mitochondrial disease in children is Leigh… (more)

Subjects/Keywords: mitochondrial disease; Leigh syndrome; massively parallel sequencing

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APA (6th Edition):

Lake, N. J. (2018). Using massively parallel sequencing to determine the genetic basis of Leigh Syndrome, the most common mitochondrial disorder affecting children. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/212134

Chicago Manual of Style (16th Edition):

Lake, Nicole Janet. “Using massively parallel sequencing to determine the genetic basis of Leigh Syndrome, the most common mitochondrial disorder affecting children.” 2018. Doctoral Dissertation, University of Melbourne. Accessed July 07, 2020. http://hdl.handle.net/11343/212134.

MLA Handbook (7th Edition):

Lake, Nicole Janet. “Using massively parallel sequencing to determine the genetic basis of Leigh Syndrome, the most common mitochondrial disorder affecting children.” 2018. Web. 07 Jul 2020.

Vancouver:

Lake NJ. Using massively parallel sequencing to determine the genetic basis of Leigh Syndrome, the most common mitochondrial disorder affecting children. [Internet] [Doctoral dissertation]. University of Melbourne; 2018. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/11343/212134.

Council of Science Editors:

Lake NJ. Using massively parallel sequencing to determine the genetic basis of Leigh Syndrome, the most common mitochondrial disorder affecting children. [Doctoral Dissertation]. University of Melbourne; 2018. Available from: http://hdl.handle.net/11343/212134


Penn State University

6. Zerr, Robert Joseph. Solution of the Within-Group Multidimensional Discrete Ordinates Transport Equations on Massively Parallel Architectures.

Degree: PhD, Nuclear Engineering, 2011, Penn State University

 The integral transport matrix method (ITMM) has been used as the kernel of new parallel solution methods for the discrete ordinates approximation of the within-group… (more)

Subjects/Keywords: neutron transport; discrete ordinates; within-group; massively parallel; spatial domain decomposition

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APA (6th Edition):

Zerr, R. J. (2011). Solution of the Within-Group Multidimensional Discrete Ordinates Transport Equations on Massively Parallel Architectures. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/11686

Chicago Manual of Style (16th Edition):

Zerr, Robert Joseph. “Solution of the Within-Group Multidimensional Discrete Ordinates Transport Equations on Massively Parallel Architectures.” 2011. Doctoral Dissertation, Penn State University. Accessed July 07, 2020. https://etda.libraries.psu.edu/catalog/11686.

MLA Handbook (7th Edition):

Zerr, Robert Joseph. “Solution of the Within-Group Multidimensional Discrete Ordinates Transport Equations on Massively Parallel Architectures.” 2011. Web. 07 Jul 2020.

Vancouver:

Zerr RJ. Solution of the Within-Group Multidimensional Discrete Ordinates Transport Equations on Massively Parallel Architectures. [Internet] [Doctoral dissertation]. Penn State University; 2011. [cited 2020 Jul 07]. Available from: https://etda.libraries.psu.edu/catalog/11686.

Council of Science Editors:

Zerr RJ. Solution of the Within-Group Multidimensional Discrete Ordinates Transport Equations on Massively Parallel Architectures. [Doctoral Dissertation]. Penn State University; 2011. Available from: https://etda.libraries.psu.edu/catalog/11686


Michigan Technological University

7. Hu, Linjia. MASSIVELY PARALLEL ALGORITHMS FOR POINT CLOUD BASED OBJECT RECOGNITION ON HETEROGENEOUS ARCHITECTURE.

Degree: PhD, Department of Computer Science, 2017, Michigan Technological University

  With the advent of new commodity depth sensors, point cloud data processing plays an increasingly important role in object recognition and perception. However, the… (more)

Subjects/Keywords: Massively parallel algorithm; object recognition; heterogeneous architecture; Computer Sciences

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APA (6th Edition):

Hu, L. (2017). MASSIVELY PARALLEL ALGORITHMS FOR POINT CLOUD BASED OBJECT RECOGNITION ON HETEROGENEOUS ARCHITECTURE. (Doctoral Dissertation). Michigan Technological University. Retrieved from http://digitalcommons.mtu.edu/etdr/508

Chicago Manual of Style (16th Edition):

Hu, Linjia. “MASSIVELY PARALLEL ALGORITHMS FOR POINT CLOUD BASED OBJECT RECOGNITION ON HETEROGENEOUS ARCHITECTURE.” 2017. Doctoral Dissertation, Michigan Technological University. Accessed July 07, 2020. http://digitalcommons.mtu.edu/etdr/508.

MLA Handbook (7th Edition):

Hu, Linjia. “MASSIVELY PARALLEL ALGORITHMS FOR POINT CLOUD BASED OBJECT RECOGNITION ON HETEROGENEOUS ARCHITECTURE.” 2017. Web. 07 Jul 2020.

Vancouver:

Hu L. MASSIVELY PARALLEL ALGORITHMS FOR POINT CLOUD BASED OBJECT RECOGNITION ON HETEROGENEOUS ARCHITECTURE. [Internet] [Doctoral dissertation]. Michigan Technological University; 2017. [cited 2020 Jul 07]. Available from: http://digitalcommons.mtu.edu/etdr/508.

Council of Science Editors:

Hu L. MASSIVELY PARALLEL ALGORITHMS FOR POINT CLOUD BASED OBJECT RECOGNITION ON HETEROGENEOUS ARCHITECTURE. [Doctoral Dissertation]. Michigan Technological University; 2017. Available from: http://digitalcommons.mtu.edu/etdr/508


University of California – San Francisco

8. Russell, Jonathan Foster. Familial Cortical Myoclonus Caused by Mutation in NOL3.

Degree: Biomedical Sciences, 2013, University of California – San Francisco

 Many neurologic diseases cause discrete episodic impairment. Study of the genes and mechanisms underlying these diseases has informed our understanding of the nervous system. Here… (more)

Subjects/Keywords: Genetics; familial cortical myoclonus; human genetics; massively parallel sequencing; myoclonus; NOL3

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APA (6th Edition):

Russell, J. F. (2013). Familial Cortical Myoclonus Caused by Mutation in NOL3. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/35r3d8kq

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Russell, Jonathan Foster. “Familial Cortical Myoclonus Caused by Mutation in NOL3.” 2013. Thesis, University of California – San Francisco. Accessed July 07, 2020. http://www.escholarship.org/uc/item/35r3d8kq.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Russell, Jonathan Foster. “Familial Cortical Myoclonus Caused by Mutation in NOL3.” 2013. Web. 07 Jul 2020.

Vancouver:

Russell JF. Familial Cortical Myoclonus Caused by Mutation in NOL3. [Internet] [Thesis]. University of California – San Francisco; 2013. [cited 2020 Jul 07]. Available from: http://www.escholarship.org/uc/item/35r3d8kq.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Russell JF. Familial Cortical Myoclonus Caused by Mutation in NOL3. [Thesis]. University of California – San Francisco; 2013. Available from: http://www.escholarship.org/uc/item/35r3d8kq

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Sydney

9. Sandaradura, Sarah. Application of massively parallel sequencing approaches in Nemaline Myopathy .

Degree: 2018, University of Sydney

 Nemaline myopathy (NM) is one of the most common forms of congenital myopathy. The traditional approach to diagnosis involved skeletal muscle biopsy followed by Sanger… (more)

Subjects/Keywords: congenital myopathy; genetic; neuromuscular; nemaline myopathy; massively parallel sequencing

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APA (6th Edition):

Sandaradura, S. (2018). Application of massively parallel sequencing approaches in Nemaline Myopathy . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/18998

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sandaradura, Sarah. “Application of massively parallel sequencing approaches in Nemaline Myopathy .” 2018. Thesis, University of Sydney. Accessed July 07, 2020. http://hdl.handle.net/2123/18998.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sandaradura, Sarah. “Application of massively parallel sequencing approaches in Nemaline Myopathy .” 2018. Web. 07 Jul 2020.

Vancouver:

Sandaradura S. Application of massively parallel sequencing approaches in Nemaline Myopathy . [Internet] [Thesis]. University of Sydney; 2018. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/2123/18998.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sandaradura S. Application of massively parallel sequencing approaches in Nemaline Myopathy . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/18998

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Washington

10. Rich, Matthew Saul. Massively parallel analysis of the functional effects of mutations.

Degree: PhD, 2017, University of Washington

Massively parallel assays can dramatically advance our understanding of biological processes. Coupling them with modern mutagenesis techniques allows for fine mapping of the link between… (more)

Subjects/Keywords: High throughput sequencing; Massively parallel; TP53; Yeast; Molecular biology; Genetics

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APA (6th Edition):

Rich, M. S. (2017). Massively parallel analysis of the functional effects of mutations. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/40589

Chicago Manual of Style (16th Edition):

Rich, Matthew Saul. “Massively parallel analysis of the functional effects of mutations.” 2017. Doctoral Dissertation, University of Washington. Accessed July 07, 2020. http://hdl.handle.net/1773/40589.

MLA Handbook (7th Edition):

Rich, Matthew Saul. “Massively parallel analysis of the functional effects of mutations.” 2017. Web. 07 Jul 2020.

Vancouver:

Rich MS. Massively parallel analysis of the functional effects of mutations. [Internet] [Doctoral dissertation]. University of Washington; 2017. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1773/40589.

Council of Science Editors:

Rich MS. Massively parallel analysis of the functional effects of mutations. [Doctoral Dissertation]. University of Washington; 2017. Available from: http://hdl.handle.net/1773/40589


University of Melbourne

11. Lim, Sze Chern. Identification of novel genes causing mitochondrial energy generation disorders.

Degree: 2012, University of Melbourne

 Intracellular energy is generated in the form of ATP via mitochondrial oxidative phosphorylation (OXPHOS). OXPHOS disorders affecting one or more of the 5 OXPHOS enzymes… (more)

Subjects/Keywords: mitochondria; massively parallel sequencing; mitochondrial disorders; molecular genetics

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APA (6th Edition):

Lim, S. C. (2012). Identification of novel genes causing mitochondrial energy generation disorders. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/37362

Chicago Manual of Style (16th Edition):

Lim, Sze Chern. “Identification of novel genes causing mitochondrial energy generation disorders.” 2012. Doctoral Dissertation, University of Melbourne. Accessed July 07, 2020. http://hdl.handle.net/11343/37362.

MLA Handbook (7th Edition):

Lim, Sze Chern. “Identification of novel genes causing mitochondrial energy generation disorders.” 2012. Web. 07 Jul 2020.

Vancouver:

Lim SC. Identification of novel genes causing mitochondrial energy generation disorders. [Internet] [Doctoral dissertation]. University of Melbourne; 2012. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/11343/37362.

Council of Science Editors:

Lim SC. Identification of novel genes causing mitochondrial energy generation disorders. [Doctoral Dissertation]. University of Melbourne; 2012. Available from: http://hdl.handle.net/11343/37362


University of Melbourne

12. Teo, Zhi Ling (Joyce). Genetic variants, phenotypic spectrum and breast cancer risk associated with germline mutations in PALB2: identifying female PALB2 mutation carriers at time of diagnosis.

Degree: 2013, University of Melbourne

 PALB2 is a breast cancer susceptibility gene which encodes a protein that is fundamental to the maintenance of genome stability via the homologous recombination DNA… (more)

Subjects/Keywords: PALB2; breast cancer; breast cancer risk; tumour morphology; massively parallel sequencing

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APA (6th Edition):

Teo, Z. L. (. (2013). Genetic variants, phenotypic spectrum and breast cancer risk associated with germline mutations in PALB2: identifying female PALB2 mutation carriers at time of diagnosis. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/38188

Chicago Manual of Style (16th Edition):

Teo, Zhi Ling (Joyce). “Genetic variants, phenotypic spectrum and breast cancer risk associated with germline mutations in PALB2: identifying female PALB2 mutation carriers at time of diagnosis.” 2013. Doctoral Dissertation, University of Melbourne. Accessed July 07, 2020. http://hdl.handle.net/11343/38188.

MLA Handbook (7th Edition):

Teo, Zhi Ling (Joyce). “Genetic variants, phenotypic spectrum and breast cancer risk associated with germline mutations in PALB2: identifying female PALB2 mutation carriers at time of diagnosis.” 2013. Web. 07 Jul 2020.

Vancouver:

Teo ZL(. Genetic variants, phenotypic spectrum and breast cancer risk associated with germline mutations in PALB2: identifying female PALB2 mutation carriers at time of diagnosis. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/11343/38188.

Council of Science Editors:

Teo ZL(. Genetic variants, phenotypic spectrum and breast cancer risk associated with germline mutations in PALB2: identifying female PALB2 mutation carriers at time of diagnosis. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/38188


University of Melbourne

13. Smith, Katherine Rose. Identifying inherited disease-causing mutations using massively parallel sequencing.

Degree: 2014, University of Melbourne

Massively parallel sequencing (MPS) technology has accelerated the rate at which mutations causing inherited Mendelian disorders are identified. In particular, whole-exome sequencing (WES) has been… (more)

Subjects/Keywords: massively parallel sequencing; monogenic disorders; genetic linkage analysis; identity by descent

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APA (6th Edition):

Smith, K. R. (2014). Identifying inherited disease-causing mutations using massively parallel sequencing. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/42055

Chicago Manual of Style (16th Edition):

Smith, Katherine Rose. “Identifying inherited disease-causing mutations using massively parallel sequencing.” 2014. Doctoral Dissertation, University of Melbourne. Accessed July 07, 2020. http://hdl.handle.net/11343/42055.

MLA Handbook (7th Edition):

Smith, Katherine Rose. “Identifying inherited disease-causing mutations using massively parallel sequencing.” 2014. Web. 07 Jul 2020.

Vancouver:

Smith KR. Identifying inherited disease-causing mutations using massively parallel sequencing. [Internet] [Doctoral dissertation]. University of Melbourne; 2014. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/11343/42055.

Council of Science Editors:

Smith KR. Identifying inherited disease-causing mutations using massively parallel sequencing. [Doctoral Dissertation]. University of Melbourne; 2014. Available from: http://hdl.handle.net/11343/42055


University of Melbourne

14. Eggers, Stefanie. Genetic analysis of Disorders of Sex Development using Massively Parallel Sequencing.

Degree: 2013, University of Melbourne

 Background: Disorders of Sexual Development (DSDs) are conditions present at birth, in which development of the gonads or external genitalia is atypical. The cause of… (more)

Subjects/Keywords: Disorders of Sex Development; DSD; Massively Parallel Sequencing; MPS

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APA (6th Edition):

Eggers, S. (2013). Genetic analysis of Disorders of Sex Development using Massively Parallel Sequencing. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/38470

Chicago Manual of Style (16th Edition):

Eggers, Stefanie. “Genetic analysis of Disorders of Sex Development using Massively Parallel Sequencing.” 2013. Doctoral Dissertation, University of Melbourne. Accessed July 07, 2020. http://hdl.handle.net/11343/38470.

MLA Handbook (7th Edition):

Eggers, Stefanie. “Genetic analysis of Disorders of Sex Development using Massively Parallel Sequencing.” 2013. Web. 07 Jul 2020.

Vancouver:

Eggers S. Genetic analysis of Disorders of Sex Development using Massively Parallel Sequencing. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/11343/38470.

Council of Science Editors:

Eggers S. Genetic analysis of Disorders of Sex Development using Massively Parallel Sequencing. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/38470


Rochester Institute of Technology

15. Muszynski, Jesse. Pond IDE: Machine level program development environment and register transfer level simulator for a massively parallel computer architecture.

Degree: Microelectronic Engineering, 2010, Rochester Institute of Technology

 As computing architectures are being implemented in late and post silicon technologies, fault tolerance and concurrent operation are becoming increasingly important. It is already common… (more)

Subjects/Keywords: Massively parallel; Multi-core; Nano architecture; Network on chip; Post silicon; Register transfer level

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APA (6th Edition):

Muszynski, J. (2010). Pond IDE: Machine level program development environment and register transfer level simulator for a massively parallel computer architecture. (Thesis). Rochester Institute of Technology. Retrieved from https://scholarworks.rit.edu/theses/7142

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Muszynski, Jesse. “Pond IDE: Machine level program development environment and register transfer level simulator for a massively parallel computer architecture.” 2010. Thesis, Rochester Institute of Technology. Accessed July 07, 2020. https://scholarworks.rit.edu/theses/7142.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Muszynski, Jesse. “Pond IDE: Machine level program development environment and register transfer level simulator for a massively parallel computer architecture.” 2010. Web. 07 Jul 2020.

Vancouver:

Muszynski J. Pond IDE: Machine level program development environment and register transfer level simulator for a massively parallel computer architecture. [Internet] [Thesis]. Rochester Institute of Technology; 2010. [cited 2020 Jul 07]. Available from: https://scholarworks.rit.edu/theses/7142.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Muszynski J. Pond IDE: Machine level program development environment and register transfer level simulator for a massively parallel computer architecture. [Thesis]. Rochester Institute of Technology; 2010. Available from: https://scholarworks.rit.edu/theses/7142

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Oklahoma State University

16. Espindola, Andres Sebastian. Massively Parallel Sequencing (Mps) As a Diagnostic and Forensic Analysis Tool for Important Fungi and Chromista Plant Pathogens.

Degree: Plant Pathology, 2013, Oklahoma State University

 Different mechanisms are involved in the movement of plant pathogens such as rainwater, wind, vectors, etc. Eukaryotic plant pathogens, and principally fungal and chromista are… (more)

Subjects/Keywords: massively parallel sequencing; next generation sequencing; phakopsora pachyrhizi; phytophthora ramorum; puccinia graminis; pythium ultimum

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APA (6th Edition):

Espindola, A. S. (2013). Massively Parallel Sequencing (Mps) As a Diagnostic and Forensic Analysis Tool for Important Fungi and Chromista Plant Pathogens. (Thesis). Oklahoma State University. Retrieved from http://hdl.handle.net/11244/11155

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Espindola, Andres Sebastian. “Massively Parallel Sequencing (Mps) As a Diagnostic and Forensic Analysis Tool for Important Fungi and Chromista Plant Pathogens.” 2013. Thesis, Oklahoma State University. Accessed July 07, 2020. http://hdl.handle.net/11244/11155.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Espindola, Andres Sebastian. “Massively Parallel Sequencing (Mps) As a Diagnostic and Forensic Analysis Tool for Important Fungi and Chromista Plant Pathogens.” 2013. Web. 07 Jul 2020.

Vancouver:

Espindola AS. Massively Parallel Sequencing (Mps) As a Diagnostic and Forensic Analysis Tool for Important Fungi and Chromista Plant Pathogens. [Internet] [Thesis]. Oklahoma State University; 2013. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/11244/11155.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Espindola AS. Massively Parallel Sequencing (Mps) As a Diagnostic and Forensic Analysis Tool for Important Fungi and Chromista Plant Pathogens. [Thesis]. Oklahoma State University; 2013. Available from: http://hdl.handle.net/11244/11155

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Texas A&M University

17. Hackemack, Michael Wayne. Higher-Order DGFEM Transport Calculations on Polytope Meshes for Massively-Parallel Architectures.

Degree: PhD, Nuclear Engineering, 2016, Texas A&M University

 In this dissertation, we develop improvements to the discrete ordinates (S_N) neutron transport equation using a Discontinuous Galerkin Finite Element Method (DGFEM) spatial discretization on… (more)

Subjects/Keywords: neutron transport; polytope basis functions; higher-order; diffusion synthetic acceleration; massively-parallel; diffusion

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APA (6th Edition):

Hackemack, M. W. (2016). Higher-Order DGFEM Transport Calculations on Polytope Meshes for Massively-Parallel Architectures. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/157991

Chicago Manual of Style (16th Edition):

Hackemack, Michael Wayne. “Higher-Order DGFEM Transport Calculations on Polytope Meshes for Massively-Parallel Architectures.” 2016. Doctoral Dissertation, Texas A&M University. Accessed July 07, 2020. http://hdl.handle.net/1969.1/157991.

MLA Handbook (7th Edition):

Hackemack, Michael Wayne. “Higher-Order DGFEM Transport Calculations on Polytope Meshes for Massively-Parallel Architectures.” 2016. Web. 07 Jul 2020.

Vancouver:

Hackemack MW. Higher-Order DGFEM Transport Calculations on Polytope Meshes for Massively-Parallel Architectures. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1969.1/157991.

Council of Science Editors:

Hackemack MW. Higher-Order DGFEM Transport Calculations on Polytope Meshes for Massively-Parallel Architectures. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/157991


University of Texas – Austin

18. Lena, Charles Manuel. Scalable electronic structure methods to solve the Kohn-Sham equation.

Degree: PhD, Chemical Engineering, 2018, University of Texas – Austin

 From the single hydrogen to proteins in the hundreds of thousands of kilodaltons, scientists can use the electronic structure of interacting atoms to predict their… (more)

Subjects/Keywords: Kohn-Sham equations; Density functional theory; High performance computing; Massively parallel computing; Electronic structure problem

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APA (6th Edition):

Lena, C. M. (2018). Scalable electronic structure methods to solve the Kohn-Sham equation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63299

Chicago Manual of Style (16th Edition):

Lena, Charles Manuel. “Scalable electronic structure methods to solve the Kohn-Sham equation.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed July 07, 2020. http://hdl.handle.net/2152/63299.

MLA Handbook (7th Edition):

Lena, Charles Manuel. “Scalable electronic structure methods to solve the Kohn-Sham equation.” 2018. Web. 07 Jul 2020.

Vancouver:

Lena CM. Scalable electronic structure methods to solve the Kohn-Sham equation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/2152/63299.

Council of Science Editors:

Lena CM. Scalable electronic structure methods to solve the Kohn-Sham equation. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/63299


University of KwaZulu-Natal

19. Ragalo, Anisa. An analysis of algorithms to estimate the characteristics of the underlying population in Massively Parallel Pyrosequencing data.

Degree: 2011, University of KwaZulu-Natal

Massively Parallel Pyrosequencing (MPP) is a next generation DNA sequencing technique that is becoming ubiquitous because it is considerably faster, cheaper and produces a higher… (more)

Subjects/Keywords: Massively Parallel Pyrosequencing (MPP).; DNA sequencing.; MPP reads.; Removal of non-authentic variation.; Computational algorithms.

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APA (6th Edition):

Ragalo, A. (2011). An analysis of algorithms to estimate the characteristics of the underlying population in Massively Parallel Pyrosequencing data. (Thesis). University of KwaZulu-Natal. Retrieved from https://researchspace.ukzn.ac.za/handle/10413/16904

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ragalo, Anisa. “An analysis of algorithms to estimate the characteristics of the underlying population in Massively Parallel Pyrosequencing data.” 2011. Thesis, University of KwaZulu-Natal. Accessed July 07, 2020. https://researchspace.ukzn.ac.za/handle/10413/16904.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ragalo, Anisa. “An analysis of algorithms to estimate the characteristics of the underlying population in Massively Parallel Pyrosequencing data.” 2011. Web. 07 Jul 2020.

Vancouver:

Ragalo A. An analysis of algorithms to estimate the characteristics of the underlying population in Massively Parallel Pyrosequencing data. [Internet] [Thesis]. University of KwaZulu-Natal; 2011. [cited 2020 Jul 07]. Available from: https://researchspace.ukzn.ac.za/handle/10413/16904.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ragalo A. An analysis of algorithms to estimate the characteristics of the underlying population in Massively Parallel Pyrosequencing data. [Thesis]. University of KwaZulu-Natal; 2011. Available from: https://researchspace.ukzn.ac.za/handle/10413/16904

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Iowa

20. Shearer, Aiden Eliot. Deafness in the genomics era.

Degree: PhD, Molecular Physiology and Biophysics, 2014, University of Iowa

  Deafness is the most common sensory deficit in humans, affecting 278 million people worldwide. Non-syndromic hearing loss (NSHL), hearing loss not associated with other… (more)

Subjects/Keywords: Deafness; Genomics; Hearing loss; Massively parallel sequencing; Targeted genomic enrichment; Usher syndrome; Biophysics

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APA (6th Edition):

Shearer, A. E. (2014). Deafness in the genomics era. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/4750

Chicago Manual of Style (16th Edition):

Shearer, Aiden Eliot. “Deafness in the genomics era.” 2014. Doctoral Dissertation, University of Iowa. Accessed July 07, 2020. https://ir.uiowa.edu/etd/4750.

MLA Handbook (7th Edition):

Shearer, Aiden Eliot. “Deafness in the genomics era.” 2014. Web. 07 Jul 2020.

Vancouver:

Shearer AE. Deafness in the genomics era. [Internet] [Doctoral dissertation]. University of Iowa; 2014. [cited 2020 Jul 07]. Available from: https://ir.uiowa.edu/etd/4750.

Council of Science Editors:

Shearer AE. Deafness in the genomics era. [Doctoral Dissertation]. University of Iowa; 2014. Available from: https://ir.uiowa.edu/etd/4750

21. Zhao, Min. Risk Measures Extracted from Option Market Data Using Massively Parallel Computing.

Degree: MS, 2011, Worcester Polytechnic Institute

  The famous Black-Scholes formula provided the first mathematically sound mechanism to price financial options. It is based on the assumption, that daily random stock… (more)

Subjects/Keywords: Financial risk management; Massively parallel GPU comtuing; Stochastic volatility model; Black-Scholes Formula

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APA (6th Edition):

Zhao, M. (2011). Risk Measures Extracted from Option Market Data Using Massively Parallel Computing. (Thesis). Worcester Polytechnic Institute. Retrieved from etd-042711-001313 ; https://digitalcommons.wpi.edu/etd-theses/373

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zhao, Min. “Risk Measures Extracted from Option Market Data Using Massively Parallel Computing.” 2011. Thesis, Worcester Polytechnic Institute. Accessed July 07, 2020. etd-042711-001313 ; https://digitalcommons.wpi.edu/etd-theses/373.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zhao, Min. “Risk Measures Extracted from Option Market Data Using Massively Parallel Computing.” 2011. Web. 07 Jul 2020.

Vancouver:

Zhao M. Risk Measures Extracted from Option Market Data Using Massively Parallel Computing. [Internet] [Thesis]. Worcester Polytechnic Institute; 2011. [cited 2020 Jul 07]. Available from: etd-042711-001313 ; https://digitalcommons.wpi.edu/etd-theses/373.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zhao M. Risk Measures Extracted from Option Market Data Using Massively Parallel Computing. [Thesis]. Worcester Polytechnic Institute; 2011. Available from: etd-042711-001313 ; https://digitalcommons.wpi.edu/etd-theses/373

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Melbourne

22. Ganesamoorthy, Devika. Cell-free DNA chimerism analysis and clinical applications.

Degree: 2013, University of Melbourne

 Cell-free DNA chimerism describes the co-existence of cell-free DNA originating from more than one individual. The most obvious examples are donor-recipient DNA mixtures in the… (more)

Subjects/Keywords: cell-free DNA; massively parallel sequencing; copy number variation; renal transplant; non-invasive prenatal diagnosis

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Ganesamoorthy, D. (2013). Cell-free DNA chimerism analysis and clinical applications. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/38584

Chicago Manual of Style (16th Edition):

Ganesamoorthy, Devika. “Cell-free DNA chimerism analysis and clinical applications.” 2013. Doctoral Dissertation, University of Melbourne. Accessed July 07, 2020. http://hdl.handle.net/11343/38584.

MLA Handbook (7th Edition):

Ganesamoorthy, Devika. “Cell-free DNA chimerism analysis and clinical applications.” 2013. Web. 07 Jul 2020.

Vancouver:

Ganesamoorthy D. Cell-free DNA chimerism analysis and clinical applications. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/11343/38584.

Council of Science Editors:

Ganesamoorthy D. Cell-free DNA chimerism analysis and clinical applications. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/38584


University of Melbourne

23. Corboy, Gregory Philip. The role of next generation sequencing in the management of haematological malignancies.

Degree: 2018, University of Melbourne

 Next generation sequencing comprises a rapidly-evolving cohort of technologies which enable detection of genetic variants present in DNA or RNA. In the context of haematological… (more)

Subjects/Keywords: genomics; next generation sequencing; massively parallel sequencing; haematology; hematology; cancer; hematological malignancies; haematological malignancies

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Corboy, G. P. (2018). The role of next generation sequencing in the management of haematological malignancies. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/218096

Chicago Manual of Style (16th Edition):

Corboy, Gregory Philip. “The role of next generation sequencing in the management of haematological malignancies.” 2018. Doctoral Dissertation, University of Melbourne. Accessed July 07, 2020. http://hdl.handle.net/11343/218096.

MLA Handbook (7th Edition):

Corboy, Gregory Philip. “The role of next generation sequencing in the management of haematological malignancies.” 2018. Web. 07 Jul 2020.

Vancouver:

Corboy GP. The role of next generation sequencing in the management of haematological malignancies. [Internet] [Doctoral dissertation]. University of Melbourne; 2018. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/11343/218096.

Council of Science Editors:

Corboy GP. The role of next generation sequencing in the management of haematological malignancies. [Doctoral Dissertation]. University of Melbourne; 2018. Available from: http://hdl.handle.net/11343/218096


University of California – Berkeley

24. Vo, Anh-Thu. Determinants and Implications of Variation in the Avian Gut Microbiota.

Degree: Integrative Biology, 2014, University of California – Berkeley

 Microbes occur in extraordinary abundance and diversity in vertebrates, and a growing body of work, particularly on humans and mice, has highlighted the pervasive role… (more)

Subjects/Keywords: Microbiology; Ecology; avian microbiology; host-associated microbiota; massively parallel sequencing; metaorganismal biology; microbial ecology; natural variation

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APA (6th Edition):

Vo, A. (2014). Determinants and Implications of Variation in the Avian Gut Microbiota. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/9xn036k9

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Vo, Anh-Thu. “Determinants and Implications of Variation in the Avian Gut Microbiota.” 2014. Thesis, University of California – Berkeley. Accessed July 07, 2020. http://www.escholarship.org/uc/item/9xn036k9.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Vo, Anh-Thu. “Determinants and Implications of Variation in the Avian Gut Microbiota.” 2014. Web. 07 Jul 2020.

Vancouver:

Vo A. Determinants and Implications of Variation in the Avian Gut Microbiota. [Internet] [Thesis]. University of California – Berkeley; 2014. [cited 2020 Jul 07]. Available from: http://www.escholarship.org/uc/item/9xn036k9.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Vo A. Determinants and Implications of Variation in the Avian Gut Microbiota. [Thesis]. University of California – Berkeley; 2014. Available from: http://www.escholarship.org/uc/item/9xn036k9

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Virginia Tech

25. Slotta, Douglas J. Structural Design Using Cellular Automata.

Degree: MS, Computer Science, 2001, Virginia Tech

 Traditional parallel methods for structural design do not scale well. This thesis discusses the application of massively scalable cellular automata (CA) techniques to structural design.… (more)

Subjects/Keywords: structural analysis; massively parallel processing; cellular automata

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APA (6th Edition):

Slotta, D. J. (2001). Structural Design Using Cellular Automata. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/33368

Chicago Manual of Style (16th Edition):

Slotta, Douglas J. “Structural Design Using Cellular Automata.” 2001. Masters Thesis, Virginia Tech. Accessed July 07, 2020. http://hdl.handle.net/10919/33368.

MLA Handbook (7th Edition):

Slotta, Douglas J. “Structural Design Using Cellular Automata.” 2001. Web. 07 Jul 2020.

Vancouver:

Slotta DJ. Structural Design Using Cellular Automata. [Internet] [Masters thesis]. Virginia Tech; 2001. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/10919/33368.

Council of Science Editors:

Slotta DJ. Structural Design Using Cellular Automata. [Masters Thesis]. Virginia Tech; 2001. Available from: http://hdl.handle.net/10919/33368

26. Poursaeed, Nasim. Genetic diagnosis and identification of novel genes in neuromuscular disorders using next generation sequencing : Diagnostic génétique et identification de nouveau gènes impliqués dans les maladies neuromusculaires par séquençage haut débit.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2012, Université de Strasbourg

Les maladies neuromusculaires sont des maladies souvent très sévères et très handicapantes, et un fardeau pour les patients, leurs familles, ainsi que pour le système… (more)

Subjects/Keywords: Maladies neuromusculaires; Myopathies centronucléaires; Séquençage haut débit; Neuromuscular disorders; Centronuclear myopathies; Massively parallel sequencing; 616.7; 660.65; 572.8

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APA (6th Edition):

Poursaeed, N. (2012). Genetic diagnosis and identification of novel genes in neuromuscular disorders using next generation sequencing : Diagnostic génétique et identification de nouveau gènes impliqués dans les maladies neuromusculaires par séquençage haut débit. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2012STRAJ055

Chicago Manual of Style (16th Edition):

Poursaeed, Nasim. “Genetic diagnosis and identification of novel genes in neuromuscular disorders using next generation sequencing : Diagnostic génétique et identification de nouveau gènes impliqués dans les maladies neuromusculaires par séquençage haut débit.” 2012. Doctoral Dissertation, Université de Strasbourg. Accessed July 07, 2020. http://www.theses.fr/2012STRAJ055.

MLA Handbook (7th Edition):

Poursaeed, Nasim. “Genetic diagnosis and identification of novel genes in neuromuscular disorders using next generation sequencing : Diagnostic génétique et identification de nouveau gènes impliqués dans les maladies neuromusculaires par séquençage haut débit.” 2012. Web. 07 Jul 2020.

Vancouver:

Poursaeed N. Genetic diagnosis and identification of novel genes in neuromuscular disorders using next generation sequencing : Diagnostic génétique et identification de nouveau gènes impliqués dans les maladies neuromusculaires par séquençage haut débit. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2012. [cited 2020 Jul 07]. Available from: http://www.theses.fr/2012STRAJ055.

Council of Science Editors:

Poursaeed N. Genetic diagnosis and identification of novel genes in neuromuscular disorders using next generation sequencing : Diagnostic génétique et identification de nouveau gènes impliqués dans les maladies neuromusculaires par séquençage haut débit. [Doctoral Dissertation]. Université de Strasbourg; 2012. Available from: http://www.theses.fr/2012STRAJ055


University of Washington

27. Rosenberg, Alexander. Learning Models of Gene Expression from Synthetic DNA Sequences.

Degree: PhD, 2016, University of Washington

 Over the past decade, new sequencing technologies have enabled the comprehensive cataloging of human genetic variation, but for most DNA sequence variants we do not… (more)

Subjects/Keywords: deep learning; gene expression; high throughput; machine learning; massively parallel reporter assay; modeling; Biology; Genetics; Computer science; electrical engineering

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APA (6th Edition):

Rosenberg, A. (2016). Learning Models of Gene Expression from Synthetic DNA Sequences. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/36609

Chicago Manual of Style (16th Edition):

Rosenberg, Alexander. “Learning Models of Gene Expression from Synthetic DNA Sequences.” 2016. Doctoral Dissertation, University of Washington. Accessed July 07, 2020. http://hdl.handle.net/1773/36609.

MLA Handbook (7th Edition):

Rosenberg, Alexander. “Learning Models of Gene Expression from Synthetic DNA Sequences.” 2016. Web. 07 Jul 2020.

Vancouver:

Rosenberg A. Learning Models of Gene Expression from Synthetic DNA Sequences. [Internet] [Doctoral dissertation]. University of Washington; 2016. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1773/36609.

Council of Science Editors:

Rosenberg A. Learning Models of Gene Expression from Synthetic DNA Sequences. [Doctoral Dissertation]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/36609


University of Oregon

28. Turnbull, Douglas William, 1979-. Genetic dissection of the transcriptional hypoxia response and genomic regional capture for massively parallel sequencing.

Degree: 2008, University of Oregon

 When cells are faced with the stress of oxygen deprivation (hypoxia), they must alter their physiology in order to survive. One adaptation cells make during… (more)

Subjects/Keywords: Bioinformatics; Genetics; Massively parallel sequencing; Hypoxia; Genetic dissection

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APA (6th Edition):

Turnbull, Douglas William, 1. (2008). Genetic dissection of the transcriptional hypoxia response and genomic regional capture for massively parallel sequencing. (Thesis). University of Oregon. Retrieved from http://hdl.handle.net/1794/9030

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Turnbull, Douglas William, 1979-. “Genetic dissection of the transcriptional hypoxia response and genomic regional capture for massively parallel sequencing.” 2008. Thesis, University of Oregon. Accessed July 07, 2020. http://hdl.handle.net/1794/9030.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Turnbull, Douglas William, 1979-. “Genetic dissection of the transcriptional hypoxia response and genomic regional capture for massively parallel sequencing.” 2008. Web. 07 Jul 2020.

Vancouver:

Turnbull, Douglas William 1. Genetic dissection of the transcriptional hypoxia response and genomic regional capture for massively parallel sequencing. [Internet] [Thesis]. University of Oregon; 2008. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1794/9030.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Turnbull, Douglas William 1. Genetic dissection of the transcriptional hypoxia response and genomic regional capture for massively parallel sequencing. [Thesis]. University of Oregon; 2008. Available from: http://hdl.handle.net/1794/9030

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Illinois – Urbana-Champaign

29. Cook, Jeffrey J. Scaling short read de novo DNA sequence assembly to gigabase genomes.

Degree: PhD, 1200, 2011, University of Illinois – Urbana-Champaign

 The recent advent of massively parallel sequencing technologies has drastically reduced the cost of sequencing, sparking a revolution in whole genome de novo sequencing. However,… (more)

Subjects/Keywords: de novo sequence assembly; de Bruijn graph; Eulerian assembly; gigabase genome assembly; Deoxyribonucleic Acid (DNA); short reads; massively parallel sequencing

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APA (6th Edition):

Cook, J. J. (2011). Scaling short read de novo DNA sequence assembly to gigabase genomes. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24291

Chicago Manual of Style (16th Edition):

Cook, Jeffrey J. “Scaling short read de novo DNA sequence assembly to gigabase genomes.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 07, 2020. http://hdl.handle.net/2142/24291.

MLA Handbook (7th Edition):

Cook, Jeffrey J. “Scaling short read de novo DNA sequence assembly to gigabase genomes.” 2011. Web. 07 Jul 2020.

Vancouver:

Cook JJ. Scaling short read de novo DNA sequence assembly to gigabase genomes. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/2142/24291.

Council of Science Editors:

Cook JJ. Scaling short read de novo DNA sequence assembly to gigabase genomes. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24291


University of Melbourne

30. Yow, Melissa-Ann. The role of infection in the aetiology of prostate cancer.

Degree: 2015, University of Melbourne

 An infectious aetiology for prostate cancer has been conjectured for decades but the evidence gained from questionnaire-based and sero-epidemiological studies is weak and inconsistent and… (more)

Subjects/Keywords: prostate cancer; sexually transmitted infections; 16S rRNA; cDNA; sequencing; massively parallel sequencing; qPCR; novel infectious agents; infection

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Yow, M. (2015). The role of infection in the aetiology of prostate cancer. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/91560

Chicago Manual of Style (16th Edition):

Yow, Melissa-Ann. “The role of infection in the aetiology of prostate cancer.” 2015. Doctoral Dissertation, University of Melbourne. Accessed July 07, 2020. http://hdl.handle.net/11343/91560.

MLA Handbook (7th Edition):

Yow, Melissa-Ann. “The role of infection in the aetiology of prostate cancer.” 2015. Web. 07 Jul 2020.

Vancouver:

Yow M. The role of infection in the aetiology of prostate cancer. [Internet] [Doctoral dissertation]. University of Melbourne; 2015. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/11343/91560.

Council of Science Editors:

Yow M. The role of infection in the aetiology of prostate cancer. [Doctoral Dissertation]. University of Melbourne; 2015. Available from: http://hdl.handle.net/11343/91560

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