Suchergebnisse - Eberle, Michael A

Allele Frequency Matching Between SNPs Reveals an Excess of Linkage Disequilibrium in Genic Regions of the Human Genome von Eberle, Michael A, Rieder, Mark J, Kruglyak, Leonid, Nickerson, Deborah A

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Sequence Variation and Linkage Disequilibrium in the Human T-Cell Receptor β (TCRB) Locus von Subrahmanyan, Lakshman, Eberle, Michael A., Clark, Andrew G., Kruglyak, Leonid, Nickerson, Deborah A.

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Selecting a Maximally Informative Set of Single-Nucleotide Polymorphisms for Association Analyses Using Linkage Disequilibrium von Carlson, Christopher S., Eberle, Michael A., Rieder, Mark J., Yi, Qian, Kruglyak, Leonid, Nickerson, Deborah A.

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Lower-Than-Expected Linkage Disequilibrium between Tightly Linked Markers in Humans Suggests a Role for Gene Conversion von Ardlie, Kristin, Liu-Cordero, Shau Neen, Eberle, Michael A., Daly, Mark, Barrett, Jeff, Winchester, Ellen, Lander, Eric S., Kruglyak, Leonid

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Population History and Natural Selection Shape Patterns of Genetic Variation in 132 Genes von Akey, Joshua M, Eberle, Michael A, Rieder, Mark J, Carlson, Christopher S, Shriver, Mark D, Nickerson, Deborah A, Kruglyak, Leonid

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Large scale in silico characterization of repeat expansion variation in human genomes von Fazal, Sarah, Danzi, Matt C., Cintra, Vivian P., Bis-Brewer, Dana M., Dolzhenko, Egor, Eberle, Michael A., Zuchner, Stephan

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Cyrius: accurate CYP2D6 genotyping using whole-genome sequencing data von Chen, Xiao, Shen, Fei, Gonzaludo, Nina, Malhotra, Alka, Rogert, Cande, Taft, Ryan J., Bentley, David R., Eberle, Michael A.

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Genomic regions exhibiting positive selection identified from dense genotype data von Carlson, Christopher S., Thomas, Daryl J., Eberle, Michael A., Swanson, Johanna E., Livingston, Robert J., Rieder, Mark J., Nickerson, Deborah A.

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Extensive and breed-specific linkage disequilibrium in Canis familiaris von Sutter, Nathan B., Eberle, Michael A., Parker, Heidi G., Pullar, Barbara J., Kirkness, Ewen F., Kruglyak, Leonid, Ostrander, Elaine A.

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Genome-wide sequencing as a first-tier screening test for short tandem repeat expansions von Rajan-Babu, Indhu-Shree, Peng, Junran J., Chiu, Readman, Li, Chenkai, Mohajeri, Arezoo, Dolzhenko, Egor, Eberle, Michael A., Birol, Inanc, Friedman, Jan M.

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Correction to: Genome-wide sequencing as a first-tier screening test for short tandem repeat expansions von Rajan-Babu, Indhu-Shree, Peng, Junran J., Chiu, Readman, Li, Chenkai, Mohajeri, Arezoo, Dolzhenko, Egor, Eberle, Michael A., Birol, Inanc, Friedman, Jan M.

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Haplotype Diversity across 100 Candidate Genes for Inflammation, Lipid Metabolism, and Blood Pressure Regulation in Two Populations von Crawford, Dana C., Carlson, Christopher S., Rieder, Mark J., Carrington, Dana P., Yi, Qian, Smith, Joshua D., Eberle, Michael A., Kruglyak, Leonid, Nickerson, Deborah A.

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Whole-genome haplotyping by dilution, amplification, and sequencing von Kaper, Fiona, Swamy, Sajani, Klotzle, Brandy, Munchel, Sarah, Cottrell, Joseph, Bibikova, Marina, Chuang, Han-Yu, Kruglyak, Semyon, Ronaghi, Mostafa, Eberle, Michael A., Fan, Jian-Bing

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Paragraph: a graph-based structural variant genotyper for short-read sequence data von Chen, Sai, Krusche, Peter, Dolzhenko, Egor, Sherman, Rachel M., Petrovski, Roman, Schlesinger, Felix, Kirsche, Melanie, Bentley, David R., Schatz, Michael C., Sedlazeck, Fritz J., Eberle, Michael A.

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A New Susceptibility Locus for Autosomal Dominant Pancreatic Cancer Maps to Chromosome 4q32-34 von Eberle, Michael A., Pfützer, Roland, Pogue-Geile, Kay L., Bronner, Mary P., Crispin, David, Kimmey, Michael B., Duerr, Richard H., Kruglyak, Leonid, Whitcomb, David C., Brentnall, Teresa A.

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Power to Detect Risk Alleles Using Genome-Wide Tag SNP Panels von Eberle, Michael A, Ng, Pauline C, Kuhn, Kenneth, Zhou, Lixin, Peiffer, Daniel A, Galver, Luana, Viaud-Martinez, Karine A, Lawley, Cynthia Taylor, Gunderson, Kevin L, Shen, Richard, Murray, Sarah S

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Comprehensive short and long read sequencing analysis for the Gaucher and Parkinson’s disease-associated GBA gene von Toffoli, Marco, Chen, Xiao, Sedlazeck, Fritz J., Lee, Chiao-Yin, Mullin, Stephen, Higgins, Abigail, Koletsi, Sofia, Garcia-Segura, Monica Emili, Sammler, Esther, Scholz, Sonja W., Schapira, Anthony H. V., Eberle, Michael A., Proukakis, Christos

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Spinal muscular atrophy diagnosis and carrier screening from genome sequencing data von Chen, Xiao, Sanchis-Juan, Alba, French, Courtney E., Connell, Andrew J., Delon, Isabelle, Kingsbury, Zoya, Chawla, Aditi, Halpern, Aaron L., Taft, Ryan J., Bentley, David R., Butchbach, Matthew E. R., Raymond, F. Lucy, Eberle, Michael A.

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A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigree von Eberle, Michael A., Fritzilas, Epameinondas, Krusche, Peter, Källberg, Morten, Moore, Benjamin L., Bekritsky, Mitchell A., Iqbal, Zamin, Chuang, Han-Yu, Humphray, Sean J., Halpern, Aaron L., Kruglyak, Semyon, Margulies, Elliott H., McVean, Gil, Bentley, David R.

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Best Practices for Benchmarking Germline Small Variant Calls in Human Genomes von Krusche, Peter, Trigg, Len, Boutros, Paul C., Mason, Christopher E., De La Vega, Francisco M., Moore, Benjamin L., Gonzalez-Porta, Mar, Eberle, Michael A., Tezak, Zivana, Lababidi, Samir, Truty, Rebecca, Asimenos, George, Funke, Birgit, Fleharty, Mark, Chapman, Brad A., Salit, Marc, Zook, Justin M

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