Global ETD Search

Search theses and dissertations gathered from participating repositories worldwide. Every result links back to the library that holds it. No account is needed.

Results

Showing 1 to 20 of 340 for “"DNA sequencing"”.

  1. Nanopore technology for DNA sequencing

    Made available in DSpace on 2010-08-20T17:58:37Z (GMT). No. of bitstreams: 3 Comer_Jeffrey.zip: 226477214 bytes, checksum: 58e732aa747f3bd4da0e576ddcc65779 (MD5) Comer_Jeffrey.pdf: 19129383 bytes, checksum: be143050e3104cb300d385ce2da0c51e (MD5) license.txt: 4062 bytes, checksum: …

    uiuc Repository record for Nanopore technology for DNA sequencing (opens in a new tab)

  2. Signal processing for DNA sequencing

    DNA sequencing is the process of determining the sequence of chemical bases in a particular DNA molecule-nature's blueprint of how life works. The advancement of biological science in has created a vast demand for sequencing methods, which needs to be addressed by automated equipment. This thesis …

    mit Repository record for Signal processing for DNA sequencing (opens in a new tab)

  3. Cell-Free Dna Sequencing In Multiple Myeloma

    … both in acute and long-term settings. Cell-free DNA, DNA fragments which are released into circulation as a part of normal cellular turnover, is a useful and dynamic biomarker in cancer patients due to the presence of circulating tumor DNA (ctDNA), which is readily identified using next …

    uthsc Repository record for Cell-Free Dna Sequencing In Multiple Myeloma (opens in a new tab)

  4. Scheduling of biological samples for DNA sequencing

    In a DNA sequencing workflow, a biological sample has to pass through multiple process steps. Two consecutive steps are hydroshearing and library construction. Samples arrive randomly into the inventory and are to complete both processes before their due dates. The research project is to decide the …

    mit Repository record for Scheduling of biological samples for DNA sequencing (opens in a new tab)

  5. Error Correction in Next Generation DNA Sequencing Data

    Motivation: High throughput Next Generation Sequencing (NGS) technologies can sequence the genome of a species quickly and cheaply. Errors that are introduced by NGS technologies limit the full potential of the applications that rely on their data. Current techniques used to correct these errors …

    uwo Repository record for Error Correction in Next Generation DNA Sequencing Data (opens in a new tab)

  6. Expanding the applications of high-throughput DNA sequencing

    DNA sequencing is the process of determining the identities of the nucleotides that make up a molecule of DNA. The rapid pace of advancements in sequencing technologies in recent years have made it possible to simultaneously determine the sequences of hundreds of millions of short DNA fragments. …

    texas Repository record for Expanding the applications of high-throughput DNA sequencing (opens in a new tab)

  7. Genome scanning : an AFM-based DNA sequencing technique

    Genome Scanning is a powerful new technique for DNA sequencing. The method presented in this thesis uses an atomic force microscope with a functionalized cantilever tip to sequence single stranded DNA immobilized to a mica surface. The functionalized cantilever tip hybridizes with only one base …

    mit Repository record for Genome scanning : an AFM-based DNA sequencing technique (opens in a new tab)

  8. Novel molecular engineering approaches for genotyping and DNA sequencing

    … (MALDI-TOF MS) offers an attractive option for DNA analysis due to its high accuracy, sensitivity and speed. In the first part of the thesis, we report the design, synthesis and evaluation of a novel set of mass tagged, cleavable biotinylated dideoxynucleotides (ddNTP-N3-biotins) for DNA

    columbia-diss Repository record for Novel molecular engineering approaches for genotyping and DNA sequencing (opens in a new tab)

  9. Computational optimisation strategies for targeted DNA sequencing using nanopores

    Long-read DNA sequencing is causing a generational shift in genome sequencing productivity and is revolutionising many aspects of biological discovery. One of the technologies behind this transformation is sequencing using nanopores that act as biosensors measuring fluctuations of an ionic current …

    cambridge Repository record for Computational optimisation strategies for targeted DNA sequencing using nanopores (opens in a new tab)

  10. Application of manufacturing tools in the DNA sequencing process

    Thesis (M.B.A.)--Massachusetts Institute of Technology, Sloan School of Management; and, (S.M.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering; in conjunction with the Leaders for Manufacturing Program at MIT, 1999.

    mit Repository record for Application of manufacturing tools in the DNA sequencing process (opens in a new tab)

  11. Measuring ongoing chromosomal instability in single-cell DNA sequencing data

    … replication status. Cancer cells often exhibit DNA copy number aberrations and can vary widely in their ploidy as a consequence. Correct estimation of the ploidy of single cell genomes is crucial for many aspects of downstream analysis, such as copy number calling and inference of cell …

    cambridge Repository record for Measuring ongoing chromosomal instability in single-cell DNA sequencing data (opens in a new tab)

  12. Development of a microfluidic platform for integrated DNA sequencing protocols

    … reduce costs and improve the quality of in the DNA sequencing methodology currently implemented at the Broad Institute in Cambridge, Massachusetts. The Sequencing Center at the Broad Institute currently generates an average of 130 million bases per day with an average read length of 800. This is …

    mit Repository record for Development of a microfluidic platform for integrated DNA sequencing protocols (opens in a new tab)

  13. Optimization of data acquisition system for novel DNA sequencing instrument

    Thesis (S.B. and M.Eng.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2000.

    mit Repository record for Optimization of data acquisition system for novel DNA sequencing instrument (opens in a new tab)

  14. Return on investment and library complexity analysis for DNA sequencing

    … the profiles of information acquisition during DNA sequencing experiments is critical to the design and implementation of large-scale studies in medical and population genetics. One known technical challenge and cost driver in next-generation sequencing data is the occurrence of non-independent …

    mit Repository record for Return on investment and library complexity analysis for DNA sequencing (opens in a new tab)

  15. An analysis of the next generation DNA sequencing technology market

    … the ongoing development of the next generation DNA sequencing market in an effort to predict exactly which factors will play a role in determining who will ultimately succeed. This will be accomplished through an analysis incorporating a combination of historical precedents in this industry and …

    mit Repository record for An analysis of the next generation DNA sequencing technology market (opens in a new tab)

  16. Error Correction and de novo Genome Assembly of DNA Sequencing Data

    … sciences. Current technologies are capable of sequencing short pieces of DNA with very high quality. These short pieces of DNA determint the sequence of bases in the genome of any species. This information is key in understanding many of the aspects of how life functions. The accuracy of …

    uwo Repository record for Error Correction and de novo Genome Assembly of DNA Sequencing Data (opens in a new tab)

  17. Integrated Analog Readout Array and Digital Backend for Mobile DNA Sequencing

    DNA, a fundamental biomolecule, contains the genetic code that governs the development, functioning, and reproduction of all living organisms. It is composed of smaller molecular units called nucleotides. The process of determining the specific sequence of these nucleotides is known as DNA

    york Repository record for Integrated Analog Readout Array and Digital Backend for Mobile DNA Sequencing (opens in a new tab)

  18. Investigating Metastatic Lineage In Colorectal Cancer By Single Cell Dna Sequencing

    … have applied conventional bulk next-generation sequencing (NGS) methods, which have limited ability to resolve intratumor heterogeneity.</p> <p>To address this problem, we have developed a highly-multiplexed single cell DNA sequencing method that combines flow-sorting of single nuclei, …

    uthsc Repository record for Investigating Metastatic Lineage In Colorectal Cancer By Single Cell Dna Sequencing (opens in a new tab)

  19. Statistical Methods For Resolving Intratumor Heterogeneity With Single-Cell Dna Sequencing

    … and treatment resistance. Single-cell DNA sequencing is a promising experimental method for studying intratumor heterogeneity, but brings unique statistical challenges in interpreting the resulting data. Researchers lack methods to determine whether sufficiently many cells have been …

    uthsc Repository record for Statistical Methods For Resolving Intratumor Heterogeneity With Single-Cell Dna Sequencing (opens in a new tab)

  20. Elucidating aquatic virioplankton diversity and dynamics using high-throughput DNA sequencing

    … ecology was the application of high-throughput DNA sequencing to entire viral communities. Known as shotgun viral metagenomics, this approach allows access to the majority of viruses that cannot be maintained in culture. Viral metagenomics has revealed surprising insight into ancient …

    udel Repository record for Elucidating aquatic virioplankton diversity and dynamics using high-throughput DNA sequencing (opens in a new tab)

Page 1 of 17