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1.
Relationship between triplet repeat polymorphisms and HapMap tagSNPs
by Keddache, Mehdi, Ph.D.  University of Cincinnati. 2011: 123 pages; 3452890.
2.
Bayesian Biclustering on Discrete Data: Variable Selection Methods
by Guo, Lei, Ph.D.  Harvard University. 2013: 143 pages; 3600176.
3.
Human genetic susceptibility to mother to child transmission of HIV: A study of mother-infant pairs in Malawi
by Joubert, Bonnie Rachel, Ph.D.  The University of North Carolina at Chapel Hill. 2009: 215 pages; 3366470.
4.
The Molecular Evolution of Athletic Endurance in Humans
by McRae, Ellen Susan Rogers, Ph.D.  Harvard University. 2011: 180 pages; 3462778.
5.
Exploring the genetic basis of chronic periodontitis: A genome-wide approach
by Divaris, Kimon, Ph.D.  The University of North Carolina at Chapel Hill. 2011: 299 pages; 3495471.
6.
Archaic admixture in modern humans
by Bohlender, Ryan James, Ph.D.  The University of Utah. 2015: 58 pages; 10019581.
8.
The genetic basis of diabetic retinopathy
by Charles, Bashira Abdullah, Ph.D.  University of Pittsburgh. 2008: 111 pages; 3349265.
10.
Ancestry Informative Markers Tailored to Hispanic Populations
by Setser, Casandra Hernandez, Ph.D.  University of North Texas Health Science Center at Fort Worth. 2020: 97 pages; 27837053.
11.
Evolutionary inferences from genome-wide data in primates
by Meyer, Wynn, Ph.D.  The University of Chicago. 2013: 226 pages; 3595949.
12.
Analysis and optimization for processing grid-scale XML datasets
by Head, Michael Reuben, Ph.D.  State University of New York at Binghamton. 2009: 121 pages; 3389637.
13.
Identification of genetic factors in disease
by Below, Jennifer E., Ph.D.  The University of Chicago. 2011: 234 pages; 3460145.
15.
On the importance of phase in improving detection of shared genomic segments
by Genovese, Giulio, Ph.D.  Dartmouth College. 2010: 119 pages; 3404529.
16.
Analysis of aberrant and normal copy-number variation of human chromosome 22
by Urban, Alexander Eckehart, Ph.D.  Yale University. 2007: 126 pages; 3293411.
17.
Leukotriene receptor gene variation and atopic asthma
by Wysocki, Kenneth James, Ph.D.  The University of Arizona. 2011: 128 pages; 3459905.
18.
Statistical models for analyzing human genetic variation
by Sankararaman, Sriram, Ph.D.  University of California, Berkeley. 2010: 164 pages; 3413553.
19.
DNA Variation in FOXP3 and DRD2 and Its Association with C-Reactive Protein
by Miller, Kimberly Nicole, M.S.  Howard University. 2012: 76 pages; 1529455.
20.
Patterns of crossing over and gene conversion in meiotic recombination
by Campbell, Christopher L., Ph.D.  Yeshiva University. 2016: 216 pages; 10165490.
22.
Characterizing the impact of single nucleotide variation in breast cancer
by Desai, Kinjal, Ph.D.  Dartmouth College. 2016: 162 pages; 10144817.
24.
Developing approaches to study human epigenetic variation
by Bjornsson, Hans Tomas, Ph.D.  The Johns Hopkins University. 2007: 189 pages; 3267881.
25.
Search and ranking in semantically rich applications
by Stoyanovich, Julia, Ph.D.  Columbia University. 2010: 220 pages; 3400637.
26.
Models and forward simulations of selection, human demography, and complex traits
by Uricchio, Lawrence Hart, Ph.D.  University of California, San Francisco. 2014: 112 pages; 3681226.
27.
The genetics of kidney transplantation outcomes and autoimmune disease
by Musone, Stacy Lynn, Ph.D.  University of California, San Francisco. 2010: 126 pages; 3398896.
28.
Efficient identification of disease causative mutations with next generation sequencing technologies
by Maranhao, Bruno, Ph.D.  University of California, San Diego. 2015: 836 pages; 3718508.
29.
Genome-wide mapping and functional analysis of copy number variation in the human genome
by Haraksingh, Rajini Rani, Ph.D.  Yale University. 2012: 185 pages; 3525284.
30.
Analysis and Visualization of Local Phylogenetic Structure within Species
by Wang, Jeremy R., Ph.D.  The University of North Carolina at Chapel Hill. 2013: 154 pages; 3562960.
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