Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Nucleotide). Showing records 1 – 30 of 1218 total matches.

[1] [2] [3] [4] [5] … [41]

Search Limiters

Last 2 Years | English Only

Department

Degrees

Levels

Languages

Country

▼ Search Limiters


University of Georgia

1. Yang, Ting. The role of the salvage pathway in nucleotide sugar biosynthesis: identification of sugar kinases and NDP-sugar pyrophosphorylases.

Degree: PhD, Biochemistry and Molecular Biology, 2011, University of Georgia

 The synthesis of polysaccharides, glycoproteins, glycolipids, glycosylated secondary metabolites and hormones requires a large number of glycosyltransferases and a constant supply of nucleotide sugars. In… (more)

Subjects/Keywords: Nucleotide sugar

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Yang, T. (2011). The role of the salvage pathway in nucleotide sugar biosynthesis: identification of sugar kinases and NDP-sugar pyrophosphorylases. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/yang_ting_201108_phd

Chicago Manual of Style (16th Edition):

Yang, Ting. “The role of the salvage pathway in nucleotide sugar biosynthesis: identification of sugar kinases and NDP-sugar pyrophosphorylases.” 2011. Doctoral Dissertation, University of Georgia. Accessed October 19, 2019. http://purl.galileo.usg.edu/uga_etd/yang_ting_201108_phd.

MLA Handbook (7th Edition):

Yang, Ting. “The role of the salvage pathway in nucleotide sugar biosynthesis: identification of sugar kinases and NDP-sugar pyrophosphorylases.” 2011. Web. 19 Oct 2019.

Vancouver:

Yang T. The role of the salvage pathway in nucleotide sugar biosynthesis: identification of sugar kinases and NDP-sugar pyrophosphorylases. [Internet] [Doctoral dissertation]. University of Georgia; 2011. [cited 2019 Oct 19]. Available from: http://purl.galileo.usg.edu/uga_etd/yang_ting_201108_phd.

Council of Science Editors:

Yang T. The role of the salvage pathway in nucleotide sugar biosynthesis: identification of sugar kinases and NDP-sugar pyrophosphorylases. [Doctoral Dissertation]. University of Georgia; 2011. Available from: http://purl.galileo.usg.edu/uga_etd/yang_ting_201108_phd


University of Hong Kong

2. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 October 19, 2019. http://hdl.handle.net/10722/235921.

MLA Handbook (7th Edition):

Law, Wai-chun. “Efficient analysis solution for DNA short-read sequencing.” 2016. Web. 19 Oct 2019.

Vancouver:

Law W. Efficient analysis solution for DNA short-read sequencing. [Internet] [Masters thesis]. University of Hong Kong; 2016. [cited 2019 Oct 19]. 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


Boston College

3. Guo, Wenyue. A study of structure and function of two enzymes in pyrimidine biosynthesis.

Degree: PhD, Chemistry, 2012, Boston College

 Nucleotides, the building blocks for nucleic acids, are essential for cell growth and replication. In E. coli the enzyme responsible for the regulation of pyrimidine… (more)

Subjects/Keywords: pyrimidine nucleotide biosynthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Guo, W. (2012). A study of structure and function of two enzymes in pyrimidine biosynthesis. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101896

Chicago Manual of Style (16th Edition):

Guo, Wenyue. “A study of structure and function of two enzymes in pyrimidine biosynthesis.” 2012. Doctoral Dissertation, Boston College. Accessed October 19, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101896.

MLA Handbook (7th Edition):

Guo, Wenyue. “A study of structure and function of two enzymes in pyrimidine biosynthesis.” 2012. Web. 19 Oct 2019.

Vancouver:

Guo W. A study of structure and function of two enzymes in pyrimidine biosynthesis. [Internet] [Doctoral dissertation]. Boston College; 2012. [cited 2019 Oct 19]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101896.

Council of Science Editors:

Guo W. A study of structure and function of two enzymes in pyrimidine biosynthesis. [Doctoral Dissertation]. Boston College; 2012. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101896


University of Guelph

4. Leung, Haley. THE EFFECTS OF A NUCLEOTIDE RICH YEAST SUPPLEMENT ON GROWTH PERFORMANCE, GASTROINTESTINAL ECOLOGY AND IMMUNE SYSTEM IN BROILER CHICKENS CHALLENGED WITH EIMERIA .

Degree: 2018, University of Guelph

 Increased antibiotic free production has increased emphasis on poultry gut health leading to evaluation of dietary alternatives such as nucleotides to improve production. Therefore, yeast… (more)

Subjects/Keywords: chickens; Eimeria; nucleotide

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Leung, H. (2018). THE EFFECTS OF A NUCLEOTIDE RICH YEAST SUPPLEMENT ON GROWTH PERFORMANCE, GASTROINTESTINAL ECOLOGY AND IMMUNE SYSTEM IN BROILER CHICKENS CHALLENGED WITH EIMERIA . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14157

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):

Leung, Haley. “THE EFFECTS OF A NUCLEOTIDE RICH YEAST SUPPLEMENT ON GROWTH PERFORMANCE, GASTROINTESTINAL ECOLOGY AND IMMUNE SYSTEM IN BROILER CHICKENS CHALLENGED WITH EIMERIA .” 2018. Thesis, University of Guelph. Accessed October 19, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14157.

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

MLA Handbook (7th Edition):

Leung, Haley. “THE EFFECTS OF A NUCLEOTIDE RICH YEAST SUPPLEMENT ON GROWTH PERFORMANCE, GASTROINTESTINAL ECOLOGY AND IMMUNE SYSTEM IN BROILER CHICKENS CHALLENGED WITH EIMERIA .” 2018. Web. 19 Oct 2019.

Vancouver:

Leung H. THE EFFECTS OF A NUCLEOTIDE RICH YEAST SUPPLEMENT ON GROWTH PERFORMANCE, GASTROINTESTINAL ECOLOGY AND IMMUNE SYSTEM IN BROILER CHICKENS CHALLENGED WITH EIMERIA . [Internet] [Thesis]. University of Guelph; 2018. [cited 2019 Oct 19]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14157.

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

Council of Science Editors:

Leung H. THE EFFECTS OF A NUCLEOTIDE RICH YEAST SUPPLEMENT ON GROWTH PERFORMANCE, GASTROINTESTINAL ECOLOGY AND IMMUNE SYSTEM IN BROILER CHICKENS CHALLENGED WITH EIMERIA . [Thesis]. University of Guelph; 2018. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14157

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


Rutgers University

5. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 October 19, 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. 19 Oct 2019.

Vancouver:

Micallef, David Ian 1. Using RNA backbone torsions to study RNA structure:. [Internet] [Masters thesis]. Rutgers University; 2010. [cited 2019 Oct 19]. 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


University of Georgia

6. Sprolden, Tracy Lashonda. Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks.

Degree: MS, Statistics, 2013, University of Georgia

 A double eQTL mapping method for identifying trans eQTLs that reduces multiple testing and increases the statistical power of eQTL mapping is described. The first… (more)

Subjects/Keywords: Single nucleotide polymorphism (SNP)

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sprolden, T. L. (2013). Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/sprolden_tracy_l_201305_ms

Chicago Manual of Style (16th Edition):

Sprolden, Tracy Lashonda. “Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks.” 2013. Masters Thesis, University of Georgia. Accessed October 19, 2019. http://purl.galileo.usg.edu/uga_etd/sprolden_tracy_l_201305_ms.

MLA Handbook (7th Edition):

Sprolden, Tracy Lashonda. “Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks.” 2013. Web. 19 Oct 2019.

Vancouver:

Sprolden TL. Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks. [Internet] [Masters thesis]. University of Georgia; 2013. [cited 2019 Oct 19]. Available from: http://purl.galileo.usg.edu/uga_etd/sprolden_tracy_l_201305_ms.

Council of Science Editors:

Sprolden TL. Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks. [Masters Thesis]. University of Georgia; 2013. Available from: http://purl.galileo.usg.edu/uga_etd/sprolden_tracy_l_201305_ms


University of Pretoria

7. Ganesan, Hamilton. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms.

Degree: Biochemistry, 2010, University of Pretoria

 Tuberculosis is one of the leading causes of mortality globally. Although this disease has been around for many generations, treatment and management of the disease… (more)

Subjects/Keywords: Nucleotide polymorphisms; Comparative genomics; UCTD

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ganesan, H. (2010). New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/25245

Chicago Manual of Style (16th Edition):

Ganesan, Hamilton. “New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms.” 2010. Doctoral Dissertation, University of Pretoria. Accessed October 19, 2019. http://hdl.handle.net/2263/25245.

MLA Handbook (7th Edition):

Ganesan, Hamilton. “New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms.” 2010. Web. 19 Oct 2019.

Vancouver:

Ganesan H. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms. [Internet] [Doctoral dissertation]. University of Pretoria; 2010. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/2263/25245.

Council of Science Editors:

Ganesan H. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms. [Doctoral Dissertation]. University of Pretoria; 2010. Available from: http://hdl.handle.net/2263/25245

8. Bhasin, Yasha. Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis.

Degree: 2009, University of Pune

Common complex disorders, also known as multifactorial disorders, are characterized by the interactions of multiple genetic and/or environmental factors that influence the expression of a… (more)

Subjects/Keywords: Biotechnology; Single Nucleotide Polymorphisms

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bhasin, Y. (2009). Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis. (Thesis). University of Pune. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/3417

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):

Bhasin, Yasha. “Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis.” 2009. Thesis, University of Pune. Accessed October 19, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/3417.

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

MLA Handbook (7th Edition):

Bhasin, Yasha. “Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis.” 2009. Web. 19 Oct 2019.

Vancouver:

Bhasin Y. Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis. [Internet] [Thesis]. University of Pune; 2009. [cited 2019 Oct 19]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/3417.

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

Council of Science Editors:

Bhasin Y. Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis. [Thesis]. University of Pune; 2009. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/3417

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


Oregon State University

9. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 October 19, 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. 19 Oct 2019.

Vancouver:

Holloway JL. Algorithms for string matching with applications in molecular biology. [Internet] [Doctoral dissertation]. Oregon State University; 2009. [cited 2019 Oct 19]. 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 Pretoria

10. [No author]. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms .

Degree: 2010, University of Pretoria

 Tuberculosis is one of the leading causes of mortality globally. Although this disease has been around for many generations, treatment and management of the disease… (more)

Subjects/Keywords: Nucleotide polymorphisms; Comparative genomics; UCTD

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

author], [. (2010). New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms . (Doctoral Dissertation). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-06042010-004142/

Chicago Manual of Style (16th Edition):

author], [No. “New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms .” 2010. Doctoral Dissertation, University of Pretoria. Accessed October 19, 2019. http://upetd.up.ac.za/thesis/available/etd-06042010-004142/.

MLA Handbook (7th Edition):

author], [No. “New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms .” 2010. Web. 19 Oct 2019.

Vancouver:

author] [. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms . [Internet] [Doctoral dissertation]. University of Pretoria; 2010. [cited 2019 Oct 19]. Available from: http://upetd.up.ac.za/thesis/available/etd-06042010-004142/.

Council of Science Editors:

author] [. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms . [Doctoral Dissertation]. University of Pretoria; 2010. Available from: http://upetd.up.ac.za/thesis/available/etd-06042010-004142/


University of Hong Kong

11. Qin, Youwen. Statistical analysis of human gastrointestinal microbiota using next generation sequencing data.

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

The human gastrointestinal tract is the niche of both commensal and pathogenic microbes which play an important role in human health. This thesis includes two… (more)

Subjects/Keywords: Nucleotide sequence; Gastrointestinal system - Microbiology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Qin, Y. (2015). Statistical analysis of human gastrointestinal microbiota using next generation sequencing data. (Masters Thesis). University of Hong Kong. Retrieved from Qin, Y. [覃友文]. (2015). Statistical analysis of human gastrointestinal microbiota using next generation sequencing data. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5719476 ; http://hdl.handle.net/10722/223622

Chicago Manual of Style (16th Edition):

Qin, Youwen. “Statistical analysis of human gastrointestinal microbiota using next generation sequencing data.” 2015. Masters Thesis, University of Hong Kong. Accessed October 19, 2019. Qin, Y. [覃友文]. (2015). Statistical analysis of human gastrointestinal microbiota using next generation sequencing data. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5719476 ; http://hdl.handle.net/10722/223622.

MLA Handbook (7th Edition):

Qin, Youwen. “Statistical analysis of human gastrointestinal microbiota using next generation sequencing data.” 2015. Web. 19 Oct 2019.

Vancouver:

Qin Y. Statistical analysis of human gastrointestinal microbiota using next generation sequencing data. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2019 Oct 19]. Available from: Qin, Y. [覃友文]. (2015). Statistical analysis of human gastrointestinal microbiota using next generation sequencing data. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5719476 ; http://hdl.handle.net/10722/223622.

Council of Science Editors:

Qin Y. Statistical analysis of human gastrointestinal microbiota using next generation sequencing data. [Masters Thesis]. University of Hong Kong; 2015. Available from: Qin, Y. [覃友文]. (2015). Statistical analysis of human gastrointestinal microbiota using next generation sequencing data. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5719476 ; http://hdl.handle.net/10722/223622


University of Hong Kong

12. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 October 19, 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. 19 Oct 2019.

Vancouver:

Luo R. An all-purpose genome assembler for next-generation sequencing reads. [Internet] [Doctoral dissertation]. University of Hong Kong; 2015. [cited 2019 Oct 19]. 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

13. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 October 19, 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. 19 Oct 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 Oct 19]. 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

14. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 October 19, 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. 19 Oct 2019.

Vancouver:

Ou M. A data management framework for clinical interpretation of human variations. [Internet] [Masters thesis]. University of Hong Kong; 2017. [cited 2019 Oct 19]. 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

15. 陈若言; Chen, Ruoyan. A new tool for detecting short inversions using next generation sequencing (NGS) data and a systematic comparison of different NGS platforms on detection sensitivities.

Degree: PhD, 2017, University of Hong Kong

Rapid development of Next Generation Sequencing (NGS) technology has substantially transformed the landscape of biomedical research. As a result, analyses based on these sequencing technologies,… (more)

Subjects/Keywords: Nucleotide sequence; Medical genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

陈若言; Chen, R. (2017). A new tool for detecting short inversions using next generation sequencing (NGS) data and a systematic comparison of different NGS platforms on detection sensitivities. (Doctoral Dissertation). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/250733

Chicago Manual of Style (16th Edition):

陈若言; Chen, Ruoyan. “A new tool for detecting short inversions using next generation sequencing (NGS) data and a systematic comparison of different NGS platforms on detection sensitivities.” 2017. Doctoral Dissertation, University of Hong Kong. Accessed October 19, 2019. http://hdl.handle.net/10722/250733.

MLA Handbook (7th Edition):

陈若言; Chen, Ruoyan. “A new tool for detecting short inversions using next generation sequencing (NGS) data and a systematic comparison of different NGS platforms on detection sensitivities.” 2017. Web. 19 Oct 2019.

Vancouver:

陈若言; Chen R. A new tool for detecting short inversions using next generation sequencing (NGS) data and a systematic comparison of different NGS platforms on detection sensitivities. [Internet] [Doctoral dissertation]. University of Hong Kong; 2017. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/10722/250733.

Council of Science Editors:

陈若言; Chen R. A new tool for detecting short inversions using next generation sequencing (NGS) data and a systematic comparison of different NGS platforms on detection sensitivities. [Doctoral Dissertation]. University of Hong Kong; 2017. Available from: http://hdl.handle.net/10722/250733


University of Hong Kong

16. 楊兆恩; Yeung, Shiu-yan. Update and evaluation of 16SpathDB, an automated comprehensive database for identification of medically important bacteria by 16S rRNA gene sequencing.

Degree: Master of Medical Sciences, 2013, University of Hong Kong

Identification of pathogens is one of the important duties of clinical microbiology laboratory. Traditionally, phenotypic tests are used to identify the bacteria. However, due to… (more)

Subjects/Keywords: Pathogenic bacteria; Nucleotide sequence

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

楊兆恩; Yeung, S. (2013). Update and evaluation of 16SpathDB, an automated comprehensive database for identification of medically important bacteria by 16S rRNA gene sequencing. (Masters Thesis). University of Hong Kong. Retrieved from Yeung, S. [楊兆恩]. (2013). Update and evaluation of 16SpathDB, an automated comprehensive database for identification of medically important bacteria by 16S rRNA gene sequencing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5091599 ; http://dx.doi.org/10.5353/th_b5091599 ; http://hdl.handle.net/10722/193552

Chicago Manual of Style (16th Edition):

楊兆恩; Yeung, Shiu-yan. “Update and evaluation of 16SpathDB, an automated comprehensive database for identification of medically important bacteria by 16S rRNA gene sequencing.” 2013. Masters Thesis, University of Hong Kong. Accessed October 19, 2019. Yeung, S. [楊兆恩]. (2013). Update and evaluation of 16SpathDB, an automated comprehensive database for identification of medically important bacteria by 16S rRNA gene sequencing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5091599 ; http://dx.doi.org/10.5353/th_b5091599 ; http://hdl.handle.net/10722/193552.

MLA Handbook (7th Edition):

楊兆恩; Yeung, Shiu-yan. “Update and evaluation of 16SpathDB, an automated comprehensive database for identification of medically important bacteria by 16S rRNA gene sequencing.” 2013. Web. 19 Oct 2019.

Vancouver:

楊兆恩; Yeung S. Update and evaluation of 16SpathDB, an automated comprehensive database for identification of medically important bacteria by 16S rRNA gene sequencing. [Internet] [Masters thesis]. University of Hong Kong; 2013. [cited 2019 Oct 19]. Available from: Yeung, S. [楊兆恩]. (2013). Update and evaluation of 16SpathDB, an automated comprehensive database for identification of medically important bacteria by 16S rRNA gene sequencing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5091599 ; http://dx.doi.org/10.5353/th_b5091599 ; http://hdl.handle.net/10722/193552.

Council of Science Editors:

楊兆恩; Yeung S. Update and evaluation of 16SpathDB, an automated comprehensive database for identification of medically important bacteria by 16S rRNA gene sequencing. [Masters Thesis]. University of Hong Kong; 2013. Available from: Yeung, S. [楊兆恩]. (2013). Update and evaluation of 16SpathDB, an automated comprehensive database for identification of medically important bacteria by 16S rRNA gene sequencing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5091599 ; http://dx.doi.org/10.5353/th_b5091599 ; http://hdl.handle.net/10722/193552


University of Hong Kong

17. 黄亚志; Huang, Yazhi. HLA typing from next generation sequencing data : strategies, methods, and applications.

Degree: PhD, 2015, University of Hong Kong

 HLA genes play a key role in the human immune system. As a result, HLA typing is very important for both clinical laboratories and biomedical… (more)

Subjects/Keywords: HLA histocompatibility antigens; Nucleotide sequence

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

黄亚志; Huang, Y. (2015). HLA typing from next generation sequencing data : strategies, methods, and applications. (Doctoral Dissertation). University of Hong Kong. Retrieved from Huang, Y. [黄亚志]. (2015). HLA typing from next generation sequencing data : strategies, methods, and applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736651. ; http://dx.doi.org/10.5353/th_b5736651 ; http://hdl.handle.net/10722/235792

Chicago Manual of Style (16th Edition):

黄亚志; Huang, Yazhi. “HLA typing from next generation sequencing data : strategies, methods, and applications.” 2015. Doctoral Dissertation, University of Hong Kong. Accessed October 19, 2019. Huang, Y. [黄亚志]. (2015). HLA typing from next generation sequencing data : strategies, methods, and applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736651. ; http://dx.doi.org/10.5353/th_b5736651 ; http://hdl.handle.net/10722/235792.

MLA Handbook (7th Edition):

黄亚志; Huang, Yazhi. “HLA typing from next generation sequencing data : strategies, methods, and applications.” 2015. Web. 19 Oct 2019.

Vancouver:

黄亚志; Huang Y. HLA typing from next generation sequencing data : strategies, methods, and applications. [Internet] [Doctoral dissertation]. University of Hong Kong; 2015. [cited 2019 Oct 19]. Available from: Huang, Y. [黄亚志]. (2015). HLA typing from next generation sequencing data : strategies, methods, and applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736651. ; http://dx.doi.org/10.5353/th_b5736651 ; http://hdl.handle.net/10722/235792.

Council of Science Editors:

黄亚志; Huang Y. HLA typing from next generation sequencing data : strategies, methods, and applications. [Doctoral Dissertation]. University of Hong Kong; 2015. Available from: Huang, Y. [黄亚志]. (2015). HLA typing from next generation sequencing data : strategies, methods, and applications. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736651. ; http://dx.doi.org/10.5353/th_b5736651 ; http://hdl.handle.net/10722/235792


University of Hong Kong

18. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 October 19, 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. 19 Oct 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 Oct 19]. 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

19. 王煒欣; Wang, Weixin. A fast and accurate model to detect germline SNPs and somatic SNVs with high-throughput sequencing.

Degree: PhD, 2014, University of Hong Kong

The rapid development of high-throughput sequencing technology provides a new chance to extend the scale and resolution of genomic research. How to efficiently and accurately… (more)

Subjects/Keywords: Nucleotide sequence; Chromosome polymorphism

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

王煒欣; Wang, W. (2014). A fast and accurate model to detect germline SNPs and somatic SNVs with high-throughput sequencing. (Doctoral Dissertation). University of Hong Kong. Retrieved from Wang, W. [王煒欣]. (2014). A fast and accurate model to detect germline SNPs and somatic SNVs with high-throughput sequencing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5185953 ; http://dx.doi.org/10.5353/th_b5185953 ; http://hdl.handle.net/10722/197115

Chicago Manual of Style (16th Edition):

王煒欣; Wang, Weixin. “A fast and accurate model to detect germline SNPs and somatic SNVs with high-throughput sequencing.” 2014. Doctoral Dissertation, University of Hong Kong. Accessed October 19, 2019. Wang, W. [王煒欣]. (2014). A fast and accurate model to detect germline SNPs and somatic SNVs with high-throughput sequencing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5185953 ; http://dx.doi.org/10.5353/th_b5185953 ; http://hdl.handle.net/10722/197115.

MLA Handbook (7th Edition):

王煒欣; Wang, Weixin. “A fast and accurate model to detect germline SNPs and somatic SNVs with high-throughput sequencing.” 2014. Web. 19 Oct 2019.

Vancouver:

王煒欣; Wang W. A fast and accurate model to detect germline SNPs and somatic SNVs with high-throughput sequencing. [Internet] [Doctoral dissertation]. University of Hong Kong; 2014. [cited 2019 Oct 19]. Available from: Wang, W. [王煒欣]. (2014). A fast and accurate model to detect germline SNPs and somatic SNVs with high-throughput sequencing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5185953 ; http://dx.doi.org/10.5353/th_b5185953 ; http://hdl.handle.net/10722/197115.

Council of Science Editors:

王煒欣; Wang W. A fast and accurate model to detect germline SNPs and somatic SNVs with high-throughput sequencing. [Doctoral Dissertation]. University of Hong Kong; 2014. Available from: Wang, W. [王煒欣]. (2014). A fast and accurate model to detect germline SNPs and somatic SNVs with high-throughput sequencing. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5185953 ; http://dx.doi.org/10.5353/th_b5185953 ; http://hdl.handle.net/10722/197115


University of Hong Kong

20. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 October 19, 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. 19 Oct 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 Oct 19]. 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


Stellenbosch University

21. Van Der Merwe, Pieter de Wet. UCTD.

Degree: MSc, Biochemistry, 2015, Stellenbosch University

ENGLISH ABSTRACT: Zygophyllum orbiculatum Welwitsch ex Oliv. from Angola and Zygophyllum stapffii Schinz from Namibia were described in the late 1800’s. Recent comparisons of these… (more)

Subjects/Keywords: Zygophyllaceae; Genomics; Nucleotide sequence

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Van Der Merwe, P. d. W. (2015). UCTD. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/96877

Chicago Manual of Style (16th Edition):

Van Der Merwe, Pieter de Wet. “UCTD.” 2015. Masters Thesis, Stellenbosch University. Accessed October 19, 2019. http://hdl.handle.net/10019.1/96877.

MLA Handbook (7th Edition):

Van Der Merwe, Pieter de Wet. “UCTD.” 2015. Web. 19 Oct 2019.

Vancouver:

Van Der Merwe PdW. UCTD. [Internet] [Masters thesis]. Stellenbosch University; 2015. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/10019.1/96877.

Council of Science Editors:

Van Der Merwe PdW. UCTD. [Masters Thesis]. Stellenbosch University; 2015. Available from: http://hdl.handle.net/10019.1/96877


Columbia University

22. Ding, Hongxu. Understand Biology Using Single Cell RNA-Sequencing.

Degree: 2018, Columbia University

 This dissertation summarizes the development of experimental and analytical tools for single cell RNA sequencing (scRNA-Seq), including 1) scPLATE-Seq, a FACS- and plate-based scRNASeq platform,… (more)

Subjects/Keywords: Biology; Nucleotide sequence; Systems biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ding, H. (2018). Understand Biology Using Single Cell RNA-Sequencing. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8Z04S0R

Chicago Manual of Style (16th Edition):

Ding, Hongxu. “Understand Biology Using Single Cell RNA-Sequencing.” 2018. Doctoral Dissertation, Columbia University. Accessed October 19, 2019. https://doi.org/10.7916/D8Z04S0R.

MLA Handbook (7th Edition):

Ding, Hongxu. “Understand Biology Using Single Cell RNA-Sequencing.” 2018. Web. 19 Oct 2019.

Vancouver:

Ding H. Understand Biology Using Single Cell RNA-Sequencing. [Internet] [Doctoral dissertation]. Columbia University; 2018. [cited 2019 Oct 19]. Available from: https://doi.org/10.7916/D8Z04S0R.

Council of Science Editors:

Ding H. Understand Biology Using Single Cell RNA-Sequencing. [Doctoral Dissertation]. Columbia University; 2018. Available from: https://doi.org/10.7916/D8Z04S0R


Vanderbilt University

23. Gandhi, Vishal V. Investigating mitochondrial deoxyribonucleotide metabolism and its role in a family of genetic diseases.

Degree: PhD, Human Genetics, 2011, Vanderbilt University

 Abnormal regulation of mitochondrial deoxyribonucleoside triphosphate pools can lead to mitochondrial DNA depletion syndromes, a set of genetic diseases associated with depletion of mitochondrial DNA.… (more)

Subjects/Keywords: depletion; dNTP; mitochondria; nucleotide; mtDNA

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gandhi, V. V. (2011). Investigating mitochondrial deoxyribonucleotide metabolism and its role in a family of genetic diseases. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-11292011-142606/ ;

Chicago Manual of Style (16th Edition):

Gandhi, Vishal V. “Investigating mitochondrial deoxyribonucleotide metabolism and its role in a family of genetic diseases.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed October 19, 2019. http://etd.library.vanderbilt.edu/available/etd-11292011-142606/ ;.

MLA Handbook (7th Edition):

Gandhi, Vishal V. “Investigating mitochondrial deoxyribonucleotide metabolism and its role in a family of genetic diseases.” 2011. Web. 19 Oct 2019.

Vancouver:

Gandhi VV. Investigating mitochondrial deoxyribonucleotide metabolism and its role in a family of genetic diseases. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2019 Oct 19]. Available from: http://etd.library.vanderbilt.edu/available/etd-11292011-142606/ ;.

Council of Science Editors:

Gandhi VV. Investigating mitochondrial deoxyribonucleotide metabolism and its role in a family of genetic diseases. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu/available/etd-11292011-142606/ ;


Vanderbilt University

24. Burns, Michael Charles. Small Molecule Modulation of the Ras-SOS Interaction in Cancer.

Degree: PhD, Biochemistry, 2014, Vanderbilt University

 Aberrant activation of the small GTPase Ras by oncogenic mutation or constitutively active upstream receptor tyrosine kinases results in the deregulation of cellular signals governing… (more)

Subjects/Keywords: Ras; SOS; nucleotide exchange

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Burns, M. C. (2014). Small Molecule Modulation of the Ras-SOS Interaction in Cancer. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-12052014-101242/ ;

Chicago Manual of Style (16th Edition):

Burns, Michael Charles. “Small Molecule Modulation of the Ras-SOS Interaction in Cancer.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed October 19, 2019. http://etd.library.vanderbilt.edu//available/etd-12052014-101242/ ;.

MLA Handbook (7th Edition):

Burns, Michael Charles. “Small Molecule Modulation of the Ras-SOS Interaction in Cancer.” 2014. Web. 19 Oct 2019.

Vancouver:

Burns MC. Small Molecule Modulation of the Ras-SOS Interaction in Cancer. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2019 Oct 19]. Available from: http://etd.library.vanderbilt.edu//available/etd-12052014-101242/ ;.

Council of Science Editors:

Burns MC. Small Molecule Modulation of the Ras-SOS Interaction in Cancer. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://etd.library.vanderbilt.edu//available/etd-12052014-101242/ ;

25. André, Joseph. Modélisation moléculaire de complexes Tubuline-Ligand : Molecular modeling of Tubulin-Ligand complexes.

Degree: Docteur es, Bioinformatique, 2012, Evry-Val d'Essonne

Les microtubules sont des polymères cylindriques de tubuline-αβ, membres du cytosquelette eucaryote. Ils possèdent une dynamique intrinsèque nécessaire à de nombreuses fonctions cellulaires telle que… (more)

Subjects/Keywords: Nucléotide; Nucleotide; Molecular dynamics; Colchicine

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

André, J. (2012). Modélisation moléculaire de complexes Tubuline-Ligand : Molecular modeling of Tubulin-Ligand complexes. (Doctoral Dissertation). Evry-Val d'Essonne. Retrieved from http://www.theses.fr/2011EVRY0026

Chicago Manual of Style (16th Edition):

André, Joseph. “Modélisation moléculaire de complexes Tubuline-Ligand : Molecular modeling of Tubulin-Ligand complexes.” 2012. Doctoral Dissertation, Evry-Val d'Essonne. Accessed October 19, 2019. http://www.theses.fr/2011EVRY0026.

MLA Handbook (7th Edition):

André, Joseph. “Modélisation moléculaire de complexes Tubuline-Ligand : Molecular modeling of Tubulin-Ligand complexes.” 2012. Web. 19 Oct 2019.

Vancouver:

André J. Modélisation moléculaire de complexes Tubuline-Ligand : Molecular modeling of Tubulin-Ligand complexes. [Internet] [Doctoral dissertation]. Evry-Val d'Essonne; 2012. [cited 2019 Oct 19]. Available from: http://www.theses.fr/2011EVRY0026.

Council of Science Editors:

André J. Modélisation moléculaire de complexes Tubuline-Ligand : Molecular modeling of Tubulin-Ligand complexes. [Doctoral Dissertation]. Evry-Val d'Essonne; 2012. Available from: http://www.theses.fr/2011EVRY0026


Central Connecticut State University

26. Bigiarelli, Krista J. Using SNP analysis to refine a genetic map for the "curly whiskers" mutation in mice.

Degree: Department of Biomolecular Sciences, 2019, Central Connecticut State University

The "curly whiskers" mutation in mice (abbreviated cw) causes recessive hair curling and may also generate a single-gene barrier to tissue-graft acceptance, a combination of… (more)

Subjects/Keywords: Single nucleotide polymorphisms.; Mice.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bigiarelli, K. J. (2019). Using SNP analysis to refine a genetic map for the "curly whiskers" mutation in mice. (Thesis). Central Connecticut State University. Retrieved from http://content.library.ccsu.edu/u?/ccsutheses,2929

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):

Bigiarelli, Krista J. “Using SNP analysis to refine a genetic map for the "curly whiskers" mutation in mice.” 2019. Thesis, Central Connecticut State University. Accessed October 19, 2019. http://content.library.ccsu.edu/u?/ccsutheses,2929.

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

MLA Handbook (7th Edition):

Bigiarelli, Krista J. “Using SNP analysis to refine a genetic map for the "curly whiskers" mutation in mice.” 2019. Web. 19 Oct 2019.

Vancouver:

Bigiarelli KJ. Using SNP analysis to refine a genetic map for the "curly whiskers" mutation in mice. [Internet] [Thesis]. Central Connecticut State University; 2019. [cited 2019 Oct 19]. Available from: http://content.library.ccsu.edu/u?/ccsutheses,2929.

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

Council of Science Editors:

Bigiarelli KJ. Using SNP analysis to refine a genetic map for the "curly whiskers" mutation in mice. [Thesis]. Central Connecticut State University; 2019. Available from: http://content.library.ccsu.edu/u?/ccsutheses,2929

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


University of Adelaide

27. Stock, Beresford Hannam. The chemistry and metabolism of tetrahydronicotinamide and its nucleotide derivatives.

Degree: 1969, University of Adelaide

Subjects/Keywords: Nicotinamide nucleotide.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Stock, B. H. (1969). The chemistry and metabolism of tetrahydronicotinamide and its nucleotide derivatives. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/20422

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):

Stock, Beresford Hannam. “The chemistry and metabolism of tetrahydronicotinamide and its nucleotide derivatives.” 1969. Thesis, University of Adelaide. Accessed October 19, 2019. http://hdl.handle.net/2440/20422.

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

MLA Handbook (7th Edition):

Stock, Beresford Hannam. “The chemistry and metabolism of tetrahydronicotinamide and its nucleotide derivatives.” 1969. Web. 19 Oct 2019.

Vancouver:

Stock BH. The chemistry and metabolism of tetrahydronicotinamide and its nucleotide derivatives. [Internet] [Thesis]. University of Adelaide; 1969. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/2440/20422.

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

Council of Science Editors:

Stock BH. The chemistry and metabolism of tetrahydronicotinamide and its nucleotide derivatives. [Thesis]. University of Adelaide; 1969. Available from: http://hdl.handle.net/2440/20422

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


San Jose State University

28. Zhang, Min. Characterization of a hydride-based HPLC column by polar molecule retention.

Degree: MS, Chemistry, 2010, San Jose State University

  The UDA column, which has undecynoic acid groups attached to the silica-hydride surface, was chromatographically characterized in this research, and the retention mechanisms are… (more)

Subjects/Keywords: HPLC; Nucleotide separation; UDA column

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zhang, M. (2010). Characterization of a hydride-based HPLC column by polar molecule retention. (Masters Thesis). San Jose State University. Retrieved from https://doi.org/10.31979/etd.nm6u-h9qf ; https://scholarworks.sjsu.edu/etd_theses/3839

Chicago Manual of Style (16th Edition):

Zhang, Min. “Characterization of a hydride-based HPLC column by polar molecule retention.” 2010. Masters Thesis, San Jose State University. Accessed October 19, 2019. https://doi.org/10.31979/etd.nm6u-h9qf ; https://scholarworks.sjsu.edu/etd_theses/3839.

MLA Handbook (7th Edition):

Zhang, Min. “Characterization of a hydride-based HPLC column by polar molecule retention.” 2010. Web. 19 Oct 2019.

Vancouver:

Zhang M. Characterization of a hydride-based HPLC column by polar molecule retention. [Internet] [Masters thesis]. San Jose State University; 2010. [cited 2019 Oct 19]. Available from: https://doi.org/10.31979/etd.nm6u-h9qf ; https://scholarworks.sjsu.edu/etd_theses/3839.

Council of Science Editors:

Zhang M. Characterization of a hydride-based HPLC column by polar molecule retention. [Masters Thesis]. San Jose State University; 2010. Available from: https://doi.org/10.31979/etd.nm6u-h9qf ; https://scholarworks.sjsu.edu/etd_theses/3839


Laurentian University

29. Baath, Simran. Genetic background and environmental effects on single nucleotide polymorphisms in the NADPH pathway .

Degree: 2018, Laurentian University

 A major focus in modern genomics is determining the connection between genotypes and quantifying phenotypes. In this connection, many factors come into play including different… (more)

Subjects/Keywords: Nucleotide polymorphisms; NADPH; phenotypes; genotypes

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Baath, S. (2018). Genetic background and environmental effects on single nucleotide polymorphisms in the NADPH pathway . (Thesis). Laurentian University. Retrieved from https://zone.biblio.laurentian.ca/handle/10219/3236

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):

Baath, Simran. “Genetic background and environmental effects on single nucleotide polymorphisms in the NADPH pathway .” 2018. Thesis, Laurentian University. Accessed October 19, 2019. https://zone.biblio.laurentian.ca/handle/10219/3236.

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

MLA Handbook (7th Edition):

Baath, Simran. “Genetic background and environmental effects on single nucleotide polymorphisms in the NADPH pathway .” 2018. Web. 19 Oct 2019.

Vancouver:

Baath S. Genetic background and environmental effects on single nucleotide polymorphisms in the NADPH pathway . [Internet] [Thesis]. Laurentian University; 2018. [cited 2019 Oct 19]. Available from: https://zone.biblio.laurentian.ca/handle/10219/3236.

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

Council of Science Editors:

Baath S. Genetic background and environmental effects on single nucleotide polymorphisms in the NADPH pathway . [Thesis]. Laurentian University; 2018. Available from: https://zone.biblio.laurentian.ca/handle/10219/3236

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


University of Limerick

30. Sheikhi, Ali. Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers.

Degree: 2014, University of Limerick

peer-reviewed

A single nucleotide polymorphism, or SNP, is a site of the genome where variation occurs within a population. Almost all SNPs have only two… (more)

Subjects/Keywords: single nucleotide polymorphism; SNP; DNA sequences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sheikhi, A. (2014). Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers. (Thesis). University of Limerick. Retrieved from http://hdl.handle.net/10344/5996

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):

Sheikhi, Ali. “Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers.” 2014. Thesis, University of Limerick. Accessed October 19, 2019. http://hdl.handle.net/10344/5996.

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

MLA Handbook (7th Edition):

Sheikhi, Ali. “Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers.” 2014. Web. 19 Oct 2019.

Vancouver:

Sheikhi A. Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers. [Internet] [Thesis]. University of Limerick; 2014. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/10344/5996.

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

Council of Science Editors:

Sheikhi A. Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers. [Thesis]. University of Limerick; 2014. Available from: http://hdl.handle.net/10344/5996

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

[1] [2] [3] [4] [5] … [41]

.