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You searched for subject:(Nucleotide sequence Data processing). Showing records 1 – 30 of 55435 total matches.

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Oregon State University

1. Holloway, James Lee. Algorithms for string matching with applications in molecular biology.

Degree: PhD, Computer Science, 2009, Oregon State University

 As the volume of genetic sequence data increases due to improved sequencing techniques and increased interest, the computational tools available to analyze the data are… (more)

Subjects/Keywords: Nucleotide sequence  – Data processing

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APA (6th Edition):

Holloway, J. L. (2009). Algorithms for string matching with applications in molecular biology. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/11518

Chicago Manual of Style (16th Edition):

Holloway, James Lee. “Algorithms for string matching with applications in molecular biology.” 2009. Doctoral Dissertation, Oregon State University. Accessed September 15, 2019. http://hdl.handle.net/1957/11518.

MLA Handbook (7th Edition):

Holloway, James Lee. “Algorithms for string matching with applications in molecular biology.” 2009. Web. 15 Sep 2019.

Vancouver:

Holloway JL. Algorithms for string matching with applications in molecular biology. [Internet] [Doctoral dissertation]. Oregon State University; 2009. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/1957/11518.

Council of Science Editors:

Holloway JL. Algorithms for string matching with applications in molecular biology. [Doctoral Dissertation]. Oregon State University; 2009. Available from: http://hdl.handle.net/1957/11518


University of Hong Kong

2. Luo, Ruibang. An all-purpose genome assembler for next-generation sequencing reads.

Degree: PhD, 2015, University of Hong Kong

There is a rapidly increasing amount of de novo genome assembly using next-generation sequencing (NGS) short reads. However, several big challenges remain to be overcome… (more)

Subjects/Keywords: Nucleotide sequence - Data processing

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APA (6th Edition):

Luo, R. (2015). An all-purpose genome assembler for next-generation sequencing reads. (Doctoral Dissertation). University of Hong Kong. Retrieved from Luo, R. [罗锐邦]. (2015). An all-purpose genome assembler for next-generation sequencing reads. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5731093 ; http://hdl.handle.net/10722/224657

Chicago Manual of Style (16th Edition):

Luo, Ruibang. “An all-purpose genome assembler for next-generation sequencing reads.” 2015. Doctoral Dissertation, University of Hong Kong. Accessed September 15, 2019. Luo, R. [罗锐邦]. (2015). An all-purpose genome assembler for next-generation sequencing reads. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5731093 ; http://hdl.handle.net/10722/224657.

MLA Handbook (7th Edition):

Luo, Ruibang. “An all-purpose genome assembler for next-generation sequencing reads.” 2015. Web. 15 Sep 2019.

Vancouver:

Luo R. An all-purpose genome assembler for next-generation sequencing reads. [Internet] [Doctoral dissertation]. University of Hong Kong; 2015. [cited 2019 Sep 15]. Available from: Luo, R. [罗锐邦]. (2015). An all-purpose genome assembler for next-generation sequencing reads. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5731093 ; http://hdl.handle.net/10722/224657.

Council of Science Editors:

Luo R. An all-purpose genome assembler for next-generation sequencing reads. [Doctoral Dissertation]. University of Hong Kong; 2015. Available from: Luo, R. [罗锐邦]. (2015). An all-purpose genome assembler for next-generation sequencing reads. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5731093 ; http://hdl.handle.net/10722/224657


University of Hong Kong

3. 王毅; Wang, Yi. Binning and annotation for metagenomic next-generation sequencing reads.

Degree: PhD, 2014, University of Hong Kong

The development of next-generation sequencing technology enables us to obtain a vast number of short reads from metagenomic samples. In metagenomic samples, the reads from… (more)

Subjects/Keywords: Nucleotide sequence - Data processing

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APA (6th Edition):

王毅; Wang, Y. (2014). Binning and annotation for metagenomic next-generation sequencing reads. (Doctoral Dissertation). University of Hong Kong. Retrieved from Wang, Y. [王毅]. (2014). Binning and annotation for metagenomic next-generation sequencing reads. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5351027 ; http://dx.doi.org/10.5353/th_b5351027 ; http://hdl.handle.net/10722/208040

Chicago Manual of Style (16th Edition):

王毅; Wang, Yi. “Binning and annotation for metagenomic next-generation sequencing reads.” 2014. Doctoral Dissertation, University of Hong Kong. Accessed September 15, 2019. Wang, Y. [王毅]. (2014). Binning and annotation for metagenomic next-generation sequencing reads. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5351027 ; http://dx.doi.org/10.5353/th_b5351027 ; http://hdl.handle.net/10722/208040.

MLA Handbook (7th Edition):

王毅; Wang, Yi. “Binning and annotation for metagenomic next-generation sequencing reads.” 2014. Web. 15 Sep 2019.

Vancouver:

王毅; Wang Y. Binning and annotation for metagenomic next-generation sequencing reads. [Internet] [Doctoral dissertation]. University of Hong Kong; 2014. [cited 2019 Sep 15]. Available from: Wang, Y. [王毅]. (2014). Binning and annotation for metagenomic next-generation sequencing reads. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5351027 ; http://dx.doi.org/10.5353/th_b5351027 ; http://hdl.handle.net/10722/208040.

Council of Science Editors:

王毅; Wang Y. Binning and annotation for metagenomic next-generation sequencing reads. [Doctoral Dissertation]. University of Hong Kong; 2014. Available from: Wang, Y. [王毅]. (2014). Binning and annotation for metagenomic next-generation sequencing reads. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5351027 ; http://dx.doi.org/10.5353/th_b5351027 ; http://hdl.handle.net/10722/208040


University of Hong Kong

4. Ou, Min. A data management framework for clinical interpretation of human variations.

Degree: M. Phil., 2017, University of Hong Kong

The emergence of high-throughput, low-cost next-generation sequencing (NGS) technologies has led to an explosion in genetic information for clinical care. The exploitation of such massive… (more)

Subjects/Keywords: Nucleotide sequence - Data processing

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APA (6th Edition):

Ou, M. (2017). A data management framework for clinical interpretation of human variations. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/241409

Chicago Manual of Style (16th Edition):

Ou, Min. “A data management framework for clinical interpretation of human variations.” 2017. Masters Thesis, University of Hong Kong. Accessed September 15, 2019. http://hdl.handle.net/10722/241409.

MLA Handbook (7th Edition):

Ou, Min. “A data management framework for clinical interpretation of human variations.” 2017. Web. 15 Sep 2019.

Vancouver:

Ou M. A data management framework for clinical interpretation of human variations. [Internet] [Masters thesis]. University of Hong Kong; 2017. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/10722/241409.

Council of Science Editors:

Ou M. A data management framework for clinical interpretation of human variations. [Masters Thesis]. University of Hong Kong; 2017. Available from: http://hdl.handle.net/10722/241409


University of Hong Kong

5. 鲍素莹; Bao, Suying. Deciphering the mechanisms of genetic disorders by high throughput genomic data.

Degree: PhD, 2013, University of Hong Kong

 A new generation of non-Sanger-based sequencing technologies, so called “next-generation” sequencing (NGS), has been changing the landscape of genetics at unprecedented speed. In particular, our… (more)

Subjects/Keywords: Nucleotide sequence - Data processing; Bioinformatics

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APA (6th Edition):

鲍素莹; Bao, S. (2013). Deciphering the mechanisms of genetic disorders by high throughput genomic data. (Doctoral Dissertation). University of Hong Kong. Retrieved from Bao, S. [鲍素莹]. (2013). Deciphering the mechanisms of genetic disorders by high throughput genomic data. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5177308 ; http://dx.doi.org/10.5353/th_b5177308 ; http://hdl.handle.net/10722/196471

Chicago Manual of Style (16th Edition):

鲍素莹; Bao, Suying. “Deciphering the mechanisms of genetic disorders by high throughput genomic data.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed September 15, 2019. Bao, S. [鲍素莹]. (2013). Deciphering the mechanisms of genetic disorders by high throughput genomic data. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5177308 ; http://dx.doi.org/10.5353/th_b5177308 ; http://hdl.handle.net/10722/196471.

MLA Handbook (7th Edition):

鲍素莹; Bao, Suying. “Deciphering the mechanisms of genetic disorders by high throughput genomic data.” 2013. Web. 15 Sep 2019.

Vancouver:

鲍素莹; Bao S. Deciphering the mechanisms of genetic disorders by high throughput genomic data. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2019 Sep 15]. Available from: Bao, S. [鲍素莹]. (2013). Deciphering the mechanisms of genetic disorders by high throughput genomic data. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5177308 ; http://dx.doi.org/10.5353/th_b5177308 ; http://hdl.handle.net/10722/196471.

Council of Science Editors:

鲍素莹; Bao S. Deciphering the mechanisms of genetic disorders by high throughput genomic data. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Bao, S. [鲍素莹]. (2013). Deciphering the mechanisms of genetic disorders by high throughput genomic data. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5177308 ; http://dx.doi.org/10.5353/th_b5177308 ; http://hdl.handle.net/10722/196471


University of Hong Kong

6. 李耀满; Li, Yaoman. Efficient methods for improving the sensitivity and accuracy of RNA alignments and structure prediction.

Degree: M. Phil., 2013, University of Hong Kong

RNA plays an important role in molecular biology. RNA sequence comparison is an important method to analysis the gene expression. Since aligning RNA reads needs… (more)

Subjects/Keywords: Nucleotide sequence - Data processing

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APA (6th Edition):

李耀满; Li, Y. (2013). Efficient methods for improving the sensitivity and accuracy of RNA alignments and structure prediction. (Masters Thesis). University of Hong Kong. Retrieved from Li, Y. [李耀满]. (2013). Efficient methods for improving the sensitivity and accuracy of RNA alignments and structure prediction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153733 ; http://dx.doi.org/10.5353/th_b5153733 ; http://hdl.handle.net/10722/195977

Chicago Manual of Style (16th Edition):

李耀满; Li, Yaoman. “Efficient methods for improving the sensitivity and accuracy of RNA alignments and structure prediction.” 2013. Masters Thesis, University of Hong Kong. Accessed September 15, 2019. Li, Y. [李耀满]. (2013). Efficient methods for improving the sensitivity and accuracy of RNA alignments and structure prediction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153733 ; http://dx.doi.org/10.5353/th_b5153733 ; http://hdl.handle.net/10722/195977.

MLA Handbook (7th Edition):

李耀满; Li, Yaoman. “Efficient methods for improving the sensitivity and accuracy of RNA alignments and structure prediction.” 2013. Web. 15 Sep 2019.

Vancouver:

李耀满; Li Y. Efficient methods for improving the sensitivity and accuracy of RNA alignments and structure prediction. [Internet] [Masters thesis]. University of Hong Kong; 2013. [cited 2019 Sep 15]. Available from: Li, Y. [李耀满]. (2013). Efficient methods for improving the sensitivity and accuracy of RNA alignments and structure prediction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153733 ; http://dx.doi.org/10.5353/th_b5153733 ; http://hdl.handle.net/10722/195977.

Council of Science Editors:

李耀满; Li Y. Efficient methods for improving the sensitivity and accuracy of RNA alignments and structure prediction. [Masters Thesis]. University of Hong Kong; 2013. Available from: Li, Y. [李耀满]. (2013). Efficient methods for improving the sensitivity and accuracy of RNA alignments and structure prediction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153733 ; http://dx.doi.org/10.5353/th_b5153733 ; http://hdl.handle.net/10722/195977


University of Hong Kong

7. Peng, Yu. Iterative de Bruijn graph assemblers for second-generation sequencing reads.

Degree: PhD, 2012, University of Hong Kong

The recent advance of second-generation sequencing technologies has made it possible to generate a vast amount of short read sequences from a DNA (cDNA) sample.… (more)

Subjects/Keywords: Nucleotide sequence - Data processing.; Sequence alignment (Bioinformatics)

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APA (6th Edition):

Peng, Y. (2012). Iterative de Bruijn graph assemblers for second-generation sequencing reads. (Doctoral Dissertation). University of Hong Kong. Retrieved from Peng, Y. [彭煜]. (2012). Iterative de Bruijn graph assemblers for second-generation sequencing reads. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5053405 ; http://dx.doi.org/10.5353/th_b5053405 ; http://hdl.handle.net/10722/188286

Chicago Manual of Style (16th Edition):

Peng, Yu. “Iterative de Bruijn graph assemblers for second-generation sequencing reads.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed September 15, 2019. Peng, Y. [彭煜]. (2012). Iterative de Bruijn graph assemblers for second-generation sequencing reads. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5053405 ; http://dx.doi.org/10.5353/th_b5053405 ; http://hdl.handle.net/10722/188286.

MLA Handbook (7th Edition):

Peng, Yu. “Iterative de Bruijn graph assemblers for second-generation sequencing reads.” 2012. Web. 15 Sep 2019.

Vancouver:

Peng Y. Iterative de Bruijn graph assemblers for second-generation sequencing reads. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2019 Sep 15]. Available from: Peng, Y. [彭煜]. (2012). Iterative de Bruijn graph assemblers for second-generation sequencing reads. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5053405 ; http://dx.doi.org/10.5353/th_b5053405 ; http://hdl.handle.net/10722/188286.

Council of Science Editors:

Peng Y. Iterative de Bruijn graph assemblers for second-generation sequencing reads. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Peng, Y. [彭煜]. (2012). Iterative de Bruijn graph assemblers for second-generation sequencing reads. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5053405 ; http://dx.doi.org/10.5353/th_b5053405 ; http://hdl.handle.net/10722/188286


University of Hong Kong

8. Wong, Kwong-leong. Next generation sequencing analysis : from monogenic to polygenic disorders.

Degree: PhD, 2015, University of Hong Kong

 Since the introduction of Next Generation Sequencing(NGS), it has quickly become a popular tool for studying monogenic and polygenic disorders. Genetic architecture between monogenic and… (more)

Subjects/Keywords: Genetic disorders; Nucleotide sequence - Data processing

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APA (6th Edition):

Wong, K. (2015). Next generation sequencing analysis : from monogenic to polygenic disorders. (Doctoral Dissertation). University of Hong Kong. Retrieved from Wong, K. [黃光亮]. (2015). Next generation sequencing analysis : from monogenic to polygenic disorders. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5731070. ; http://dx.doi.org/10.5353/th_b5731070 ; http://hdl.handle.net/10722/237858

Chicago Manual of Style (16th Edition):

Wong, Kwong-leong. “Next generation sequencing analysis : from monogenic to polygenic disorders.” 2015. Doctoral Dissertation, University of Hong Kong. Accessed September 15, 2019. Wong, K. [黃光亮]. (2015). Next generation sequencing analysis : from monogenic to polygenic disorders. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5731070. ; http://dx.doi.org/10.5353/th_b5731070 ; http://hdl.handle.net/10722/237858.

MLA Handbook (7th Edition):

Wong, Kwong-leong. “Next generation sequencing analysis : from monogenic to polygenic disorders.” 2015. Web. 15 Sep 2019.

Vancouver:

Wong K. Next generation sequencing analysis : from monogenic to polygenic disorders. [Internet] [Doctoral dissertation]. University of Hong Kong; 2015. [cited 2019 Sep 15]. Available from: Wong, K. [黃光亮]. (2015). Next generation sequencing analysis : from monogenic to polygenic disorders. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5731070. ; http://dx.doi.org/10.5353/th_b5731070 ; http://hdl.handle.net/10722/237858.

Council of Science Editors:

Wong K. Next generation sequencing analysis : from monogenic to polygenic disorders. [Doctoral Dissertation]. University of Hong Kong; 2015. Available from: Wong, K. [黃光亮]. (2015). Next generation sequencing analysis : from monogenic to polygenic disorders. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5731070. ; http://dx.doi.org/10.5353/th_b5731070 ; http://hdl.handle.net/10722/237858


Massey University

9. McComish, Bennet James. Exploring biological sequence space : selected problems in sequence analysis and phylogenetics.

Degree: PhD, Computational Biology, 2012, Massey University

 As the volume and complexity of available sequence data continues to grow at an exponential rate, the need for new sequence analysis techniques becomes more… (more)

Subjects/Keywords: Nucleotide sequence; Phlyogeny; Bioinformatics; Methodology; Data processing

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APA (6th Edition):

McComish, B. J. (2012). Exploring biological sequence space : selected problems in sequence analysis and phylogenetics. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/4945

Chicago Manual of Style (16th Edition):

McComish, Bennet James. “Exploring biological sequence space : selected problems in sequence analysis and phylogenetics.” 2012. Doctoral Dissertation, Massey University. Accessed September 15, 2019. http://hdl.handle.net/10179/4945.

MLA Handbook (7th Edition):

McComish, Bennet James. “Exploring biological sequence space : selected problems in sequence analysis and phylogenetics.” 2012. Web. 15 Sep 2019.

Vancouver:

McComish BJ. Exploring biological sequence space : selected problems in sequence analysis and phylogenetics. [Internet] [Doctoral dissertation]. Massey University; 2012. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/10179/4945.

Council of Science Editors:

McComish BJ. Exploring biological sequence space : selected problems in sequence analysis and phylogenetics. [Doctoral Dissertation]. Massey University; 2012. Available from: http://hdl.handle.net/10179/4945


Western Carolina University

10. Smith, Brandon Chase. Low-level variant detection in human mitochondrial DNA using the Illumina MiSeq next-generation sequencing (NGS) platform.

Degree: 2013, Western Carolina University

 When challenged by difficult biological samples, the forensic analyst is far more likely to obtain useful data by sequencing the human mitochondrial DNA (mtDNA). Nextgeneration… (more)

Subjects/Keywords: Mitochondrial DNA  – Variation  – Data processing; Human genetics  – Variation  – Data processing; Nucleotide sequence  – Data processing

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APA (6th Edition):

Smith, B. C. (2013). Low-level variant detection in human mitochondrial DNA using the Illumina MiSeq next-generation sequencing (NGS) platform. (Masters Thesis). Western Carolina University. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=16635

Chicago Manual of Style (16th Edition):

Smith, Brandon Chase. “Low-level variant detection in human mitochondrial DNA using the Illumina MiSeq next-generation sequencing (NGS) platform.” 2013. Masters Thesis, Western Carolina University. Accessed September 15, 2019. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=16635.

MLA Handbook (7th Edition):

Smith, Brandon Chase. “Low-level variant detection in human mitochondrial DNA using the Illumina MiSeq next-generation sequencing (NGS) platform.” 2013. Web. 15 Sep 2019.

Vancouver:

Smith BC. Low-level variant detection in human mitochondrial DNA using the Illumina MiSeq next-generation sequencing (NGS) platform. [Internet] [Masters thesis]. Western Carolina University; 2013. [cited 2019 Sep 15]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=16635.

Council of Science Editors:

Smith BC. Low-level variant detection in human mitochondrial DNA using the Illumina MiSeq next-generation sequencing (NGS) platform. [Masters Thesis]. Western Carolina University; 2013. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=16635


University of Hong Kong

11. 劉兵行; Liu, Binghang. Large genome de novo assembly with bi-directional BWT.

Degree: M. Phil., 2015, University of Hong Kong

De novo genome assembly is a fundamental problem in genomics research. When assembling large genomes, time is often a very important concern, and one might… (more)

Subjects/Keywords: Data compression (Computer science); Nucleotide sequence - Data processing

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APA (6th Edition):

劉兵行; Liu, B. (2015). Large genome de novo assembly with bi-directional BWT. (Masters Thesis). University of Hong Kong. Retrieved from Liu, B. [劉兵行]. (2015). Large genome de novo assembly with bi-directional BWT. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736698 ; http://hdl.handle.net/10722/225227

Chicago Manual of Style (16th Edition):

劉兵行; Liu, Binghang. “Large genome de novo assembly with bi-directional BWT.” 2015. Masters Thesis, University of Hong Kong. Accessed September 15, 2019. Liu, B. [劉兵行]. (2015). Large genome de novo assembly with bi-directional BWT. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736698 ; http://hdl.handle.net/10722/225227.

MLA Handbook (7th Edition):

劉兵行; Liu, Binghang. “Large genome de novo assembly with bi-directional BWT.” 2015. Web. 15 Sep 2019.

Vancouver:

劉兵行; Liu B. Large genome de novo assembly with bi-directional BWT. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2019 Sep 15]. Available from: Liu, B. [劉兵行]. (2015). Large genome de novo assembly with bi-directional BWT. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736698 ; http://hdl.handle.net/10722/225227.

Council of Science Editors:

劉兵行; Liu B. Large genome de novo assembly with bi-directional BWT. [Masters Thesis]. University of Hong Kong; 2015. Available from: Liu, B. [劉兵行]. (2015). Large genome de novo assembly with bi-directional BWT. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736698 ; http://hdl.handle.net/10722/225227


University of Hong Kong

12. Gui, Hongsheng. Data mining of post genome-wide association studies and next generation sequencing.

Degree: PhD, 2013, University of Hong Kong

 Genome-wide association studies (GWAS) have been successfully applied to several complex diseases, yielding many confirmed associations. Nonetheless, at most they have explained half the genetic… (more)

Subjects/Keywords: Molecular genetics; Nucleotide sequence - Data processing; Data mining

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APA (6th Edition):

Gui, H. (2013). Data mining of post genome-wide association studies and next generation sequencing. (Doctoral Dissertation). University of Hong Kong. Retrieved from Gui, H. [桂宏胜]. (2013). Data mining of post genome-wide association studies and next generation sequencing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5106519 ; http://hdl.handle.net/10722/193419

Chicago Manual of Style (16th Edition):

Gui, Hongsheng. “Data mining of post genome-wide association studies and next generation sequencing.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed September 15, 2019. Gui, H. [桂宏胜]. (2013). Data mining of post genome-wide association studies and next generation sequencing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5106519 ; http://hdl.handle.net/10722/193419.

MLA Handbook (7th Edition):

Gui, Hongsheng. “Data mining of post genome-wide association studies and next generation sequencing.” 2013. Web. 15 Sep 2019.

Vancouver:

Gui H. Data mining of post genome-wide association studies and next generation sequencing. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2019 Sep 15]. Available from: Gui, H. [桂宏胜]. (2013). Data mining of post genome-wide association studies and next generation sequencing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5106519 ; http://hdl.handle.net/10722/193419.

Council of Science Editors:

Gui H. Data mining of post genome-wide association studies and next generation sequencing. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Gui, H. [桂宏胜]. (2013). Data mining of post genome-wide association studies and next generation sequencing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5106519 ; http://hdl.handle.net/10722/193419


University of Hong Kong

13. Zeng, Shuai. Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach.

Degree: PhD, 2014, University of Hong Kong

 The rapidly developing sequencing technology has brought up an opportunity to scientists to look into the detailed genotype information in human genome. Computational programs have… (more)

Subjects/Keywords: Medical genetics; Nucleotide sequence - Data processing; Mutation (Biology)

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

APA (6th Edition):

Zeng, S. (2014). Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach. (Doctoral Dissertation). University of Hong Kong. Retrieved from Zeng, S. [曾帥]. (2014). Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5204922 ; http://dx.doi.org/10.5353/th_b5204922 ; http://hdl.handle.net/10722/198818

Chicago Manual of Style (16th Edition):

Zeng, Shuai. “Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach.” 2014. Doctoral Dissertation, University of Hong Kong. Accessed September 15, 2019. Zeng, S. [曾帥]. (2014). Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5204922 ; http://dx.doi.org/10.5353/th_b5204922 ; http://hdl.handle.net/10722/198818.

MLA Handbook (7th Edition):

Zeng, Shuai. “Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach.” 2014. Web. 15 Sep 2019.

Vancouver:

Zeng S. Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach. [Internet] [Doctoral dissertation]. University of Hong Kong; 2014. [cited 2019 Sep 15]. Available from: Zeng, S. [曾帥]. (2014). Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5204922 ; http://dx.doi.org/10.5353/th_b5204922 ; http://hdl.handle.net/10722/198818.

Council of Science Editors:

Zeng S. Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach. [Doctoral Dissertation]. University of Hong Kong; 2014. Available from: Zeng, S. [曾帥]. (2014). Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5204922 ; http://dx.doi.org/10.5353/th_b5204922 ; http://hdl.handle.net/10722/198818


Hong Kong University of Science and Technology

14. Wang, Zhenggang. Improved algorithm for entropic segmentation of DNA sequence.

Degree: 2004, Hong Kong University of Science and Technology

 The research of Gene Predicting Algorithms is a key section in bioinformatics. After brief introduction to bioinformatics, we introduce a new and improved Gene Predicting… (more)

Subjects/Keywords: Nucleotide sequence  – Mathematical models; Nucleotide sequence  – Data processing

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

APA (6th Edition):

Wang, Z. (2004). Improved algorithm for entropic segmentation of DNA sequence. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b837481 ; http://repository.ust.hk/ir/bitstream/1783.1-5445/1/th_redirect.html

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):

Wang, Zhenggang. “Improved algorithm for entropic segmentation of DNA sequence.” 2004. Thesis, Hong Kong University of Science and Technology. Accessed September 15, 2019. https://doi.org/10.14711/thesis-b837481 ; http://repository.ust.hk/ir/bitstream/1783.1-5445/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Wang, Zhenggang. “Improved algorithm for entropic segmentation of DNA sequence.” 2004. Web. 15 Sep 2019.

Vancouver:

Wang Z. Improved algorithm for entropic segmentation of DNA sequence. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2004. [cited 2019 Sep 15]. Available from: https://doi.org/10.14711/thesis-b837481 ; http://repository.ust.hk/ir/bitstream/1783.1-5445/1/th_redirect.html.

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

Council of Science Editors:

Wang Z. Improved algorithm for entropic segmentation of DNA sequence. [Thesis]. Hong Kong University of Science and Technology; 2004. Available from: https://doi.org/10.14711/thesis-b837481 ; http://repository.ust.hk/ir/bitstream/1783.1-5445/1/th_redirect.html

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


University of Hong Kong

15. Wong, Kwong-leong. Next generation sequencing analysis : from monogenic to polygenic disorders.

Degree: PhD, 2015, University of Hong Kong

abstract

Psychiatry

Doctoral

Doctor of Philosophy

Subjects/Keywords: Nucleotide sequence - Data processing; Genetic disorders

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

APA (6th Edition):

Wong, K. (2015). Next generation sequencing analysis : from monogenic to polygenic disorders. (Doctoral Dissertation). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/224639

Chicago Manual of Style (16th Edition):

Wong, Kwong-leong. “Next generation sequencing analysis : from monogenic to polygenic disorders.” 2015. Doctoral Dissertation, University of Hong Kong. Accessed September 15, 2019. http://hdl.handle.net/10722/224639.

MLA Handbook (7th Edition):

Wong, Kwong-leong. “Next generation sequencing analysis : from monogenic to polygenic disorders.” 2015. Web. 15 Sep 2019.

Vancouver:

Wong K. Next generation sequencing analysis : from monogenic to polygenic disorders. [Internet] [Doctoral dissertation]. University of Hong Kong; 2015. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/10722/224639.

Council of Science Editors:

Wong K. Next generation sequencing analysis : from monogenic to polygenic disorders. [Doctoral Dissertation]. University of Hong Kong; 2015. Available from: http://hdl.handle.net/10722/224639


Hong Kong University of Science and Technology

16. Yang, Jianfeng. Cancer genome analysis by AluScan.

Degree: 2015, Hong Kong University of Science and Technology

 AluScan is a pre-sequencing capture method with reduced costs and cancerous DNA sample requirement, using inter-Alu PCR in conjunction with next-generation sequencing (NGS). As an… (more)

Subjects/Keywords: Human genome; Analysis; Human genetics; Variation; Nucleotide sequence; Data processing; Cancer genes

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APA (6th Edition):

Yang, J. (2015). Cancer genome analysis by AluScan. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1515018 ; http://repository.ust.hk/ir/bitstream/1783.1-87418/1/th_redirect.html

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):

Yang, Jianfeng. “Cancer genome analysis by AluScan.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed September 15, 2019. https://doi.org/10.14711/thesis-b1515018 ; http://repository.ust.hk/ir/bitstream/1783.1-87418/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Yang, Jianfeng. “Cancer genome analysis by AluScan.” 2015. Web. 15 Sep 2019.

Vancouver:

Yang J. Cancer genome analysis by AluScan. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2019 Sep 15]. Available from: https://doi.org/10.14711/thesis-b1515018 ; http://repository.ust.hk/ir/bitstream/1783.1-87418/1/th_redirect.html.

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

Council of Science Editors:

Yang J. Cancer genome analysis by AluScan. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: https://doi.org/10.14711/thesis-b1515018 ; http://repository.ust.hk/ir/bitstream/1783.1-87418/1/th_redirect.html

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


University of Hong Kong

17. Leung, Chi-ming. Motif discovery for DNA sequences.

Degree: PhD, 2006, University of Hong Kong

published_or_final_version

abstract

Computer Science

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Chin, FYL.

Subjects/Keywords: Bioinformatics.; Algorithms.; Nucleotide sequence - Data processing.

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APA (6th Edition):

Leung, C. (2006). Motif discovery for DNA sequences. (Doctoral Dissertation). University of Hong Kong. Retrieved from Leung, C. [梁志銘]. (2006). Motif discovery for DNA sequences. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3859755 ; http://dx.doi.org/10.5353/th_b3859755 ; http://hdl.handle.net/10722/50823

Chicago Manual of Style (16th Edition):

Leung, Chi-ming. “Motif discovery for DNA sequences.” 2006. Doctoral Dissertation, University of Hong Kong. Accessed September 15, 2019. Leung, C. [梁志銘]. (2006). Motif discovery for DNA sequences. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3859755 ; http://dx.doi.org/10.5353/th_b3859755 ; http://hdl.handle.net/10722/50823.

MLA Handbook (7th Edition):

Leung, Chi-ming. “Motif discovery for DNA sequences.” 2006. Web. 15 Sep 2019.

Vancouver:

Leung C. Motif discovery for DNA sequences. [Internet] [Doctoral dissertation]. University of Hong Kong; 2006. [cited 2019 Sep 15]. Available from: Leung, C. [梁志銘]. (2006). Motif discovery for DNA sequences. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3859755 ; http://dx.doi.org/10.5353/th_b3859755 ; http://hdl.handle.net/10722/50823.

Council of Science Editors:

Leung C. Motif discovery for DNA sequences. [Doctoral Dissertation]. University of Hong Kong; 2006. Available from: Leung, C. [梁志銘]. (2006). Motif discovery for DNA sequences. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3859755 ; http://dx.doi.org/10.5353/th_b3859755 ; http://hdl.handle.net/10722/50823


Simon Fraser University

18. Feng, Ping. Using blast, fasta and hybridization theory to select C. elegans genomic DNA sequence from databases that would hybridize with opsin cDNA probes.

Degree: 1997, Simon Fraser University

Subjects/Keywords: Nucleotide sequence  – Data processing.; DNA  – Analysis.

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APA (6th Edition):

Feng, P. (1997). Using blast, fasta and hybridization theory to select C. elegans genomic DNA sequence from databases that would hybridize with opsin cDNA probes. (Thesis). Simon Fraser University. Retrieved from http://summit.sfu.ca/item/7368

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):

Feng, Ping. “Using blast, fasta and hybridization theory to select C. elegans genomic DNA sequence from databases that would hybridize with opsin cDNA probes.” 1997. Thesis, Simon Fraser University. Accessed September 15, 2019. http://summit.sfu.ca/item/7368.

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

MLA Handbook (7th Edition):

Feng, Ping. “Using blast, fasta and hybridization theory to select C. elegans genomic DNA sequence from databases that would hybridize with opsin cDNA probes.” 1997. Web. 15 Sep 2019.

Vancouver:

Feng P. Using blast, fasta and hybridization theory to select C. elegans genomic DNA sequence from databases that would hybridize with opsin cDNA probes. [Internet] [Thesis]. Simon Fraser University; 1997. [cited 2019 Sep 15]. Available from: http://summit.sfu.ca/item/7368.

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

Council of Science Editors:

Feng P. Using blast, fasta and hybridization theory to select C. elegans genomic DNA sequence from databases that would hybridize with opsin cDNA probes. [Thesis]. Simon Fraser University; 1997. Available from: http://summit.sfu.ca/item/7368

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

19. Sotiriades, Euripides. Reconfigurable architecture structures for the BLAST DNA sequencing algorithm.

Degree: 2011, Technical University of Crete (TUC); Πολυτεχνείο Κρήτης

 Computational Molecular Biology or Bioinformatics is an emerging area for Electronic and Computer Engineering. Bioinformatics research results are expected to have a great impact on… (more)

Subjects/Keywords: Bioinformatics; Molecular biology; Data processing; Nucleotide sequence; Field programmable gate arrays (FPGA)

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APA (6th Edition):

Sotiriades, E. (2011). Reconfigurable architecture structures for the BLAST DNA sequencing algorithm. (Thesis). Technical University of Crete (TUC); Πολυτεχνείο Κρήτης. Retrieved from http://hdl.handle.net/10442/hedi/32018

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):

Sotiriades, Euripides. “Reconfigurable architecture structures for the BLAST DNA sequencing algorithm.” 2011. Thesis, Technical University of Crete (TUC); Πολυτεχνείο Κρήτης. Accessed September 15, 2019. http://hdl.handle.net/10442/hedi/32018.

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

MLA Handbook (7th Edition):

Sotiriades, Euripides. “Reconfigurable architecture structures for the BLAST DNA sequencing algorithm.” 2011. Web. 15 Sep 2019.

Vancouver:

Sotiriades E. Reconfigurable architecture structures for the BLAST DNA sequencing algorithm. [Internet] [Thesis]. Technical University of Crete (TUC); Πολυτεχνείο Κρήτης; 2011. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/10442/hedi/32018.

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

Council of Science Editors:

Sotiriades E. Reconfigurable architecture structures for the BLAST DNA sequencing algorithm. [Thesis]. Technical University of Crete (TUC); Πολυτεχνείο Κρήτης; 2011. Available from: http://hdl.handle.net/10442/hedi/32018

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


University of Hong Kong

20. 陳沛儀.; Chan, Pui-yee. A study on predicting gene relationship from a computational perspective.

Degree: M. Phil., 2004, University of Hong Kong

abstract

published_or_final_version

toc

Computer Science and Information Systems

Master

Master of Philosophy

Subjects/Keywords: Genomes - Data processing.; Nucleotide sequence - Data processing.; Computational biology.

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APA (6th Edition):

陳沛儀.; Chan, P. (2004). A study on predicting gene relationship from a computational perspective. (Masters Thesis). University of Hong Kong. Retrieved from Chan, P. [陳沛儀]. (2004). A study on predicting gene relationship from a computational perspective. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3046135 ; http://dx.doi.org/10.5353/th_b3046135 ; http://hdl.handle.net/10722/31311

Chicago Manual of Style (16th Edition):

陳沛儀.; Chan, Pui-yee. “A study on predicting gene relationship from a computational perspective.” 2004. Masters Thesis, University of Hong Kong. Accessed September 15, 2019. Chan, P. [陳沛儀]. (2004). A study on predicting gene relationship from a computational perspective. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3046135 ; http://dx.doi.org/10.5353/th_b3046135 ; http://hdl.handle.net/10722/31311.

MLA Handbook (7th Edition):

陳沛儀.; Chan, Pui-yee. “A study on predicting gene relationship from a computational perspective.” 2004. Web. 15 Sep 2019.

Vancouver:

陳沛儀.; Chan P. A study on predicting gene relationship from a computational perspective. [Internet] [Masters thesis]. University of Hong Kong; 2004. [cited 2019 Sep 15]. Available from: Chan, P. [陳沛儀]. (2004). A study on predicting gene relationship from a computational perspective. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3046135 ; http://dx.doi.org/10.5353/th_b3046135 ; http://hdl.handle.net/10722/31311.

Council of Science Editors:

陳沛儀.; Chan P. A study on predicting gene relationship from a computational perspective. [Masters Thesis]. University of Hong Kong; 2004. Available from: Chan, P. [陳沛儀]. (2004). A study on predicting gene relationship from a computational perspective. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3046135 ; http://dx.doi.org/10.5353/th_b3046135 ; http://hdl.handle.net/10722/31311


Hong Kong University of Science and Technology

21. Siu, Kim-Man. A computational estimation of errors in model genomes using exactly duplicated DNA sequences.

Degree: 2005, Hong Kong University of Science and Technology

 Genomes of several eukaryotic model organisms have now been finished, among them yeast (Saccharomyces cerevisiae), worm (Caenorhabditis elegans), fly (Drosophila melanogasta), mustard weed (Arabidopsis thaliana),… (more)

Subjects/Keywords: Genomics  – Mathematical models; Nucleotide sequence  – Mathematical models; Nucleotide sequence  – Data processing

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

APA (6th Edition):

Siu, K. (2005). A computational estimation of errors in model genomes using exactly duplicated DNA sequences. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b909288 ; http://repository.ust.hk/ir/bitstream/1783.1-5155/1/th_redirect.html

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):

Siu, Kim-Man. “A computational estimation of errors in model genomes using exactly duplicated DNA sequences.” 2005. Thesis, Hong Kong University of Science and Technology. Accessed September 15, 2019. https://doi.org/10.14711/thesis-b909288 ; http://repository.ust.hk/ir/bitstream/1783.1-5155/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Siu, Kim-Man. “A computational estimation of errors in model genomes using exactly duplicated DNA sequences.” 2005. Web. 15 Sep 2019.

Vancouver:

Siu K. A computational estimation of errors in model genomes using exactly duplicated DNA sequences. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2005. [cited 2019 Sep 15]. Available from: https://doi.org/10.14711/thesis-b909288 ; http://repository.ust.hk/ir/bitstream/1783.1-5155/1/th_redirect.html.

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

Council of Science Editors:

Siu K. A computational estimation of errors in model genomes using exactly duplicated DNA sequences. [Thesis]. Hong Kong University of Science and Technology; 2005. Available from: https://doi.org/10.14711/thesis-b909288 ; http://repository.ust.hk/ir/bitstream/1783.1-5155/1/th_redirect.html

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


University of Hong Kong

22. 桂宏胜; Gui, Hongsheng. Data mining of post genome-wide association studies and next generation sequencing.

Degree: PhD, 2013, University of Hong Kong

abstract

Psychiatry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Tam, PKH, Sham, PC, Garcia-Barcelo, MM, Cherny, SS.

Subjects/Keywords: Molecular genetics; Nucleotide sequence - Data processing; Data mining

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

APA (6th Edition):

桂宏胜; Gui, H. (2013). Data mining of post genome-wide association studies and next generation sequencing. (Doctoral Dissertation). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/193431

Chicago Manual of Style (16th Edition):

桂宏胜; Gui, Hongsheng. “Data mining of post genome-wide association studies and next generation sequencing.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed September 15, 2019. http://hdl.handle.net/10722/193431.

MLA Handbook (7th Edition):

桂宏胜; Gui, Hongsheng. “Data mining of post genome-wide association studies and next generation sequencing.” 2013. Web. 15 Sep 2019.

Vancouver:

桂宏胜; Gui H. Data mining of post genome-wide association studies and next generation sequencing. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/10722/193431.

Council of Science Editors:

桂宏胜; Gui H. Data mining of post genome-wide association studies and next generation sequencing. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: http://hdl.handle.net/10722/193431


University of Alberta

23. Driga, Adrian Radu. Parallel FastLSA: a parallel algorithm for pairwise sequence alignment.

Degree: MS, Department of Computing Science, 2002, University of Alberta

Subjects/Keywords: Parallel algorithms.; Nucleotide sequence – Data processing.; Amino acid sequence – Data processing.

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

APA (6th Edition):

Driga, A. R. (2002). Parallel FastLSA: a parallel algorithm for pairwise sequence alignment. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/dn39x334c

Chicago Manual of Style (16th Edition):

Driga, Adrian Radu. “Parallel FastLSA: a parallel algorithm for pairwise sequence alignment.” 2002. Masters Thesis, University of Alberta. Accessed September 15, 2019. https://era.library.ualberta.ca/files/dn39x334c.

MLA Handbook (7th Edition):

Driga, Adrian Radu. “Parallel FastLSA: a parallel algorithm for pairwise sequence alignment.” 2002. Web. 15 Sep 2019.

Vancouver:

Driga AR. Parallel FastLSA: a parallel algorithm for pairwise sequence alignment. [Internet] [Masters thesis]. University of Alberta; 2002. [cited 2019 Sep 15]. Available from: https://era.library.ualberta.ca/files/dn39x334c.

Council of Science Editors:

Driga AR. Parallel FastLSA: a parallel algorithm for pairwise sequence alignment. [Masters Thesis]. University of Alberta; 2002. Available from: https://era.library.ualberta.ca/files/dn39x334c


University of Hong Kong

24. Yim, Cheuk-hon, Terence. Approximate string alignment and its application to ESTs, mRNAs and genome mapping.

Degree: M. Phil., 2004, University of Hong Kong

published_or_final_version

abstract

Computer Science and Information Systems

Master

Master of Philosophy

Advisors/Committee Members: Ting, HF, Yiu, SM.

Subjects/Keywords: Molecular biology - Data processing.; Nucleotide sequence - Data processing.; Algorithms.; Gene mapping - Data processing

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APA (6th Edition):

Yim, Cheuk-hon, T. (2004). Approximate string alignment and its application to ESTs, mRNAs and genome mapping. (Masters Thesis). University of Hong Kong. Retrieved from Yim, C. T. [嚴卓漢]. (2004). Approximate string alignment and its application to ESTs, mRNAs and genome mapping. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3145573 ; http://dx.doi.org/10.5353/th_b3145573 ; http://hdl.handle.net/10722/39992

Chicago Manual of Style (16th Edition):

Yim, Cheuk-hon, Terence. “Approximate string alignment and its application to ESTs, mRNAs and genome mapping.” 2004. Masters Thesis, University of Hong Kong. Accessed September 15, 2019. Yim, C. T. [嚴卓漢]. (2004). Approximate string alignment and its application to ESTs, mRNAs and genome mapping. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3145573 ; http://dx.doi.org/10.5353/th_b3145573 ; http://hdl.handle.net/10722/39992.

MLA Handbook (7th Edition):

Yim, Cheuk-hon, Terence. “Approximate string alignment and its application to ESTs, mRNAs and genome mapping.” 2004. Web. 15 Sep 2019.

Vancouver:

Yim, Cheuk-hon T. Approximate string alignment and its application to ESTs, mRNAs and genome mapping. [Internet] [Masters thesis]. University of Hong Kong; 2004. [cited 2019 Sep 15]. Available from: Yim, C. T. [嚴卓漢]. (2004). Approximate string alignment and its application to ESTs, mRNAs and genome mapping. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3145573 ; http://dx.doi.org/10.5353/th_b3145573 ; http://hdl.handle.net/10722/39992.

Council of Science Editors:

Yim, Cheuk-hon T. Approximate string alignment and its application to ESTs, mRNAs and genome mapping. [Masters Thesis]. University of Hong Kong; 2004. Available from: Yim, C. T. [嚴卓漢]. (2004). Approximate string alignment and its application to ESTs, mRNAs and genome mapping. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3145573 ; http://dx.doi.org/10.5353/th_b3145573 ; http://hdl.handle.net/10722/39992


Universidade Federal de Mato Grosso do Sul

25. Sousa Júnior, Sérgio Ronaldo Alves de. Remontagem de Genomas: uma Avaliação das Técnicas de novo e por Comparação .

Degree: 2012, Universidade Federal de Mato Grosso do Sul

 As técnicas de sequenciamento de nova geração são alternativas ao método Sanger de sequenciamento. Essas técnicas produzem um grande volume de reads por ciclo de… (more)

Subjects/Keywords: Genoma - processamento de dados; Genomes - data processing; Sequenciamento de Nucleotídeo; Nucleotide Sequence; Código Genético; Genetic Code; Bioinformática; Bioinformatics; Biologia Molecular - processamento de dados; Molecular Biology - data processing

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APA (6th Edition):

Sousa Júnior, S. R. A. d. (2012). Remontagem de Genomas: uma Avaliação das Técnicas de novo e por Comparação . (Thesis). Universidade Federal de Mato Grosso do Sul. Retrieved from http://repositorio.cbc.ufms.br:8080/jspui/handle/123456789/1660

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):

Sousa Júnior, Sérgio Ronaldo Alves de. “Remontagem de Genomas: uma Avaliação das Técnicas de novo e por Comparação .” 2012. Thesis, Universidade Federal de Mato Grosso do Sul. Accessed September 15, 2019. http://repositorio.cbc.ufms.br:8080/jspui/handle/123456789/1660.

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

MLA Handbook (7th Edition):

Sousa Júnior, Sérgio Ronaldo Alves de. “Remontagem de Genomas: uma Avaliação das Técnicas de novo e por Comparação .” 2012. Web. 15 Sep 2019.

Vancouver:

Sousa Júnior SRAd. Remontagem de Genomas: uma Avaliação das Técnicas de novo e por Comparação . [Internet] [Thesis]. Universidade Federal de Mato Grosso do Sul; 2012. [cited 2019 Sep 15]. Available from: http://repositorio.cbc.ufms.br:8080/jspui/handle/123456789/1660.

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

Council of Science Editors:

Sousa Júnior SRAd. Remontagem de Genomas: uma Avaliação das Técnicas de novo e por Comparação . [Thesis]. Universidade Federal de Mato Grosso do Sul; 2012. Available from: http://repositorio.cbc.ufms.br:8080/jspui/handle/123456789/1660

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


Hong Kong University of Science and Technology

26. Yang, Guangyuan. Permutation tests for genome-wide association studies.

Degree: 2014, Hong Kong University of Science and Technology

 In genome wide association studies (GWAS), there are single-nucleotide polymorphism (SNP) pairs which have significant associations with diseases via the combination of their main effects… (more)

Subjects/Keywords: Single nucleotide polymorphisms; Testing; Data processing

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

APA (6th Edition):

Yang, G. (2014). Permutation tests for genome-wide association studies. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1432208 ; http://repository.ust.hk/ir/bitstream/1783.1-88026/1/th_redirect.html

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):

Yang, Guangyuan. “Permutation tests for genome-wide association studies.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed September 15, 2019. https://doi.org/10.14711/thesis-b1432208 ; http://repository.ust.hk/ir/bitstream/1783.1-88026/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Yang, Guangyuan. “Permutation tests for genome-wide association studies.” 2014. Web. 15 Sep 2019.

Vancouver:

Yang G. Permutation tests for genome-wide association studies. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2019 Sep 15]. Available from: https://doi.org/10.14711/thesis-b1432208 ; http://repository.ust.hk/ir/bitstream/1783.1-88026/1/th_redirect.html.

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

Council of Science Editors:

Yang G. Permutation tests for genome-wide association studies. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: https://doi.org/10.14711/thesis-b1432208 ; http://repository.ust.hk/ir/bitstream/1783.1-88026/1/th_redirect.html

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


University of Hong Kong

27. Ho, Ngai-lam. Algorithms on constrained sequence alignment.

Degree: M. Phil., 2004, University of Hong Kong

toc

abstract

published_or_final_version

Computer Science and Information Systems

Master

Master of Philosophy

Advisors/Committee Members: Chin, FYL, Lam, TW.

Subjects/Keywords: Nucleotide sequence.; Bioinformatics.; Algorithms.; Molecular biology - Data processing.; Proteins - Analysis.

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

APA (6th Edition):

Ho, N. (2004). Algorithms on constrained sequence alignment. (Masters Thesis). University of Hong Kong. Retrieved from Ho, N. [何毅林]. (2004). Algorithms on constrained sequence alignment. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3020194 ; http://dx.doi.org/10.5353/th_b3020194 ; http://hdl.handle.net/10722/31575

Chicago Manual of Style (16th Edition):

Ho, Ngai-lam. “Algorithms on constrained sequence alignment.” 2004. Masters Thesis, University of Hong Kong. Accessed September 15, 2019. Ho, N. [何毅林]. (2004). Algorithms on constrained sequence alignment. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3020194 ; http://dx.doi.org/10.5353/th_b3020194 ; http://hdl.handle.net/10722/31575.

MLA Handbook (7th Edition):

Ho, Ngai-lam. “Algorithms on constrained sequence alignment.” 2004. Web. 15 Sep 2019.

Vancouver:

Ho N. Algorithms on constrained sequence alignment. [Internet] [Masters thesis]. University of Hong Kong; 2004. [cited 2019 Sep 15]. Available from: Ho, N. [何毅林]. (2004). Algorithms on constrained sequence alignment. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3020194 ; http://dx.doi.org/10.5353/th_b3020194 ; http://hdl.handle.net/10722/31575.

Council of Science Editors:

Ho N. Algorithms on constrained sequence alignment. [Masters Thesis]. University of Hong Kong; 2004. Available from: Ho, N. [何毅林]. (2004). Algorithms on constrained sequence alignment. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3020194 ; http://dx.doi.org/10.5353/th_b3020194 ; http://hdl.handle.net/10722/31575


Western Carolina University

28. Russell, David Austin. Whole genome DNA sequence analysis of Salmonella Enterica subspecies isolated from environmental soil and fecal samples in Western North Carolina.

Degree: 2015, Western Carolina University

 Foodborne bacterial pathogens like Salmonella genera remain of interest to regulatory agencieslike the FDA and CDC. As a foodborne pathogen, capable of causing serious illness… (more)

Subjects/Keywords: Salmonella  – North Carolina, Western; Salmonella  – North Carolina  – Piedmont Triad; Environmental sampling  – North Carolina  – Piedmont Triad; Environmental sampling  – North Carolina, Western; Nucleotide sequence  – Data processing

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

APA (6th Edition):

Russell, D. A. (2015). Whole genome DNA sequence analysis of Salmonella Enterica subspecies isolated from environmental soil and fecal samples in Western North Carolina. (Masters Thesis). Western Carolina University. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=18976

Chicago Manual of Style (16th Edition):

Russell, David Austin. “Whole genome DNA sequence analysis of Salmonella Enterica subspecies isolated from environmental soil and fecal samples in Western North Carolina.” 2015. Masters Thesis, Western Carolina University. Accessed September 15, 2019. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=18976.

MLA Handbook (7th Edition):

Russell, David Austin. “Whole genome DNA sequence analysis of Salmonella Enterica subspecies isolated from environmental soil and fecal samples in Western North Carolina.” 2015. Web. 15 Sep 2019.

Vancouver:

Russell DA. Whole genome DNA sequence analysis of Salmonella Enterica subspecies isolated from environmental soil and fecal samples in Western North Carolina. [Internet] [Masters thesis]. Western Carolina University; 2015. [cited 2019 Sep 15]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=18976.

Council of Science Editors:

Russell DA. Whole genome DNA sequence analysis of Salmonella Enterica subspecies isolated from environmental soil and fecal samples in Western North Carolina. [Masters Thesis]. Western Carolina University; 2015. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=18976


University of Hong Kong

29. Law, Wai-chun. Efficient analysis solution for DNA short-read sequencing.

Degree: M. Phil., 2016, University of Hong Kong

In recent years, the demand for DNA sequencing analysis has been boosted with the advance of DNA sequencing technologies; exceeding the capacities of high-end computer… (more)

Subjects/Keywords: Nucleotide sequence - Methodology

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

APA (6th Edition):

Law, W. (2016). Efficient analysis solution for DNA short-read sequencing. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/235921

Chicago Manual of Style (16th Edition):

Law, Wai-chun. “Efficient analysis solution for DNA short-read sequencing.” 2016. Masters Thesis, University of Hong Kong. Accessed September 15, 2019. http://hdl.handle.net/10722/235921.

MLA Handbook (7th Edition):

Law, Wai-chun. “Efficient analysis solution for DNA short-read sequencing.” 2016. Web. 15 Sep 2019.

Vancouver:

Law W. Efficient analysis solution for DNA short-read sequencing. [Internet] [Masters thesis]. University of Hong Kong; 2016. [cited 2019 Sep 15]. Available from: http://hdl.handle.net/10722/235921.

Council of Science Editors:

Law W. Efficient analysis solution for DNA short-read sequencing. [Masters Thesis]. University of Hong Kong; 2016. Available from: http://hdl.handle.net/10722/235921


Rutgers University

30. Micallef, David Ian, 1979-. Using RNA backbone torsions to study RNA structure:.

Degree: MS, Microbiology and Molecular Genetics, 2010, Rutgers University

 Ribonucleic Acid (RNA) is an important cellular macromolecule vital to most if not all life on Earth. RNA has many different roles in the cell,… (more)

Subjects/Keywords: RNA; Nucleotide sequence

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

APA (6th Edition):

Micallef, David Ian, 1. (2010). Using RNA backbone torsions to study RNA structure:. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052134

Chicago Manual of Style (16th Edition):

Micallef, David Ian, 1979-. “Using RNA backbone torsions to study RNA structure:.” 2010. Masters Thesis, Rutgers University. Accessed September 15, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052134.

MLA Handbook (7th Edition):

Micallef, David Ian, 1979-. “Using RNA backbone torsions to study RNA structure:.” 2010. Web. 15 Sep 2019.

Vancouver:

Micallef, David Ian 1. Using RNA backbone torsions to study RNA structure:. [Internet] [Masters thesis]. Rutgers University; 2010. [cited 2019 Sep 15]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052134.

Council of Science Editors:

Micallef, David Ian 1. Using RNA backbone torsions to study RNA structure:. [Masters Thesis]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052134

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