Hakutulokset - Eberle, Michael A

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

Hae kokoteksti Hae kokoteksti Hae kokoteksti

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

Hae kokoteksti Hae kokoteksti

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

Hae kokoteksti Hae kokoteksti

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

Hae kokoteksti Hae kokoteksti

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

Hae kokoteksti Hae kokoteksti Hae kokoteksti

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

Hae kokoteksti Hae kokoteksti Hae kokoteksti

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

Hae kokoteksti Hae kokoteksti Hae kokoteksti

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

Hae kokoteksti Hae kokoteksti Hae kokoteksti

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

Hae kokoteksti Hae kokoteksti Hae kokoteksti

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

Hae kokoteksti Hae kokoteksti Hae kokoteksti

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

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Haplotype Diversity across 100 Candidate Genes for Inflammation, Lipid Metabolism, and Blood Pressure Regulation in Two Populations Tekijä 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.

Hae kokoteksti Hae kokoteksti

Whole-genome haplotyping by dilution, amplification, and sequencing Tekijä 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

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Paragraph: a graph-based structural variant genotyper for short-read sequence data Tekijä 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.

Hae kokoteksti Hae kokoteksti Hae kokoteksti

A New Susceptibility Locus for Autosomal Dominant Pancreatic Cancer Maps to Chromosome 4q32-34 Tekijä 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.

Hae kokoteksti Hae kokoteksti

Power to Detect Risk Alleles Using Genome-Wide Tag SNP Panels Tekijä 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

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Comprehensive short and long read sequencing analysis for the Gaucher and Parkinson’s disease-associated GBA gene Tekijä 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

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Spinal muscular atrophy diagnosis and carrier screening from genome sequencing data Tekijä 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.

Hae kokoteksti Hae kokoteksti Hae kokoteksti

A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigree Tekijä 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.

Hae kokoteksti Hae kokoteksti Hae kokoteksti

Best Practices for Benchmarking Germline Small Variant Calls in Human Genomes Tekijä 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

Hae kokoteksti Hae kokoteksti Hae kokoteksti