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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Familial Studies in Whole Exome and Genome Sequencing

Farlow, Janice L. January 2015 (has links)
Indiana University-Purdue University Indianapolis (IUPUI) / Population genetics has been revolutionized by the advent of high-throughput sequencing (HTS) methods in the 21st century. Modern day sequencers are now capable of sequencing entire exomes and genomes at unprecedented speed and accuracy. An explosion of bioinformatics software and data analysis tools now makes sequencing accessible for gene discovery in both rare Mendelian and complex disease. Family-based sequencing studies in particular have great potential for elucidating the genetic basis for many more diseases. We apply both whole exome and genome sequencing to three different cases of familial disease: intracranial aneurysm (IA), Parkinson disease (PD), and X-linked ataxia dementia (XLAD). IA and PD are both common, complex traits that inflict a devastating disease burden worldwide, mostly due to few effective therapeutic interventions. Little of the heritability of both IA and PD has been explained to date, especially as it relates to the impact of rare variation on disease. XLAD is an extremely rare neurological disease described thus far in one kindred. Although promising results have been achieved through previous genetic study designs, the causative gene has not yet been identified. For all three diseases, HTS offers an opportunity to explore the role of rare variation in disease pathogenesis. In each study, we explore the opportunities and challenges of family-based HTS for different disease models. The work presented herein contributes effective practices for study design, analysis, and interpretation in a rapidly growing field still replete with questions about how best to implement HTS in studying familial disease.
2

Characterization of circulating free DNA in healthy and diseased individuals / Maniesh van der Vaart

Van der Vaart, Maniesh January 2009 (has links)
Thesis (Ph.D. (Biochemistry))--North-West University, Potchefstroom Campus, 2009.
3

Characterization of circulating free DNA in healthy and diseased individuals / Maniesh van der Vaart

Van der Vaart, Maniesh January 2009 (has links)
Thesis (Ph.D. (Biochemistry))--North-West University, Potchefstroom Campus, 2009.
4

Exploring the Sequence Landscape of the Four-helix Bundle Protein ROP using DeepSequencing

Panneerselvam, Nishanthi January 2013 (has links)
No description available.
5

Structural and synthetic studies on biologically interesting peptides

Daley, Donald John January 1987 (has links)
No description available.
6

A molecular genetic analysis of yeast chromosome IX

Smith, Victoria January 1992 (has links)
No description available.
7

Studies on the Epstein-Barr virus genome

Gibson, T. J. January 1984 (has links)
No description available.
8

Neuroanatomy and phylogeny of cannabinoid signalling

Egertova, Michaela January 1999 (has links)
No description available.
9

Novel peptide discovery : isolation and characterisation of peptides with antidiabetic properties from the skin secretions of amphibians

Marenah, Lamin January 2001 (has links)
No description available.
10

The physical map of the genome of Caenorhabditis elegans

Coulson, Alan Robert January 1994 (has links)
No description available.

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