Arama Sonuçları - Nelson, Stanley F.

Improved variant discovery through local re-alignment of short-read next-generation sequencing data using SRMA Yazar: Homer, Nils, Nelson, Stanley F

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The frontiers of sequencing in undiagnosed neurodevelopmental diseases Yazar: Lee, Hane, Nelson, Stanley F.

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Whole genome amplification using a degenerate oligonucleotide primer allows hundreds of genotypes to be performed on less than one nanogram of genomic DNA Yazar: Cheung, Vivian G., Nelson, Stanley F.

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Calculating the statistical significance of rare variants causal for Mendelian and complex disorders Yazar: Rao, Aliz R., Nelson, Stanley F.

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COVID‐19 drug repurposing: Summary statistics on current clinical trials and promising untested candidates Yazar: Ulm, J. Wes, Nelson, Stanley F.

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Local alignment of two-base encoded DNA sequence Yazar: Homer, Nils, Merriman, Barry, Nelson, Stanley F

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BFAST: An Alignment Tool for Large Scale Genome Resequencing Yazar: Homer, Nils, Merriman, Barry, Nelson, Stanley F.

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Local alignment of generalized k-base encoded DNA sequence Yazar: Homer, Nils, Nelson, Stanley F, Merriman, Barry

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SeqWare Query Engine: storing and searching sequence data in the cloud Yazar: O’Connor, Brian D, Merriman, Barry, Nelson, Stanley F

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Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia Yazar: Chang, Vivian Y, Basso, Giuseppe, Sakamoto, Kathleen M, Nelson, Stanley F

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Emerging genetic therapies to treat Duchenne muscular dystrophy Yazar: Nelson, Stanley F., Crosbie, Rachelle H., Miceli, M. Carrie, Spencer, Melissa J.

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Rare deleterious mutations are associated with disease in bipolar disorder families Yazar: Rao, Aliz R, Yourshaw, Michael, Christensen, Bryce, Nelson, Stanley F, Kerner, Berit

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Ppp1r1b-lncRNA inhibits PRC2 at myogenic regulatory genes to promote cardiac and skeletal muscle development in mouse and human Yazar: Kang, Xuedong, Zhao, Yan, Van Arsdell, Glen, Nelson, Stanley F., Touma, Marlin

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Calpain 3 and CaMKIIβ signaling are required to induce HSP70 necessary for adaptive muscle growth after atrophy Yazar: Kramerova, Irina, Torres, Jorge A, Eskin, Ascia, Nelson, Stanley F, Spencer, Melissa J

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Rich annotation of DNA sequencing variants by leveraging the Ensembl Variant Effect Predictor with plugins Yazar: Yourshaw, Michael, Taylor, S. Paige, Rao, Aliz R., Martín, Martín G., Nelson, Stanley F.

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Gene connectivity, function, and sequence conservation: predictions from modular yeast co-expression networks Yazar: Carlson, Marc RJ, Zhang, Bin, Fang, Zixing, Mischel, Paul S, Horvath, Steve, Nelson, Stanley F

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Celsius: a community resource for Affymetrix microarray data Yazar: Day, Allen, Carlson, Marc RJ, Dong, Jun, O'Connor, Brian D, Nelson, Stanley F

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Phenotypic and Genetic Analysis of a Large Family With Migraine-Associated Vertigo Yazar: Lee, Hane, Jen, Joanna C., Cha, Yoon-Hee, Nelson, Stanley F., Baloh, Robert W.

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Rare Genomic Variants Link Bipolar Disorder with Anxiety Disorders to CREB-Regulated Intracellular Signaling Pathways Yazar: Kerner, Berit, Rao, Aliz R., Christensen, Bryce, Dandekar, Sugandha, Yourshaw, Michael, Nelson, Stanley F.

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Whole Exome Sequencing of Pediatric Gastric Adenocarcinoma Reveals an Atypical Presentation of Li-Fraumeni Syndrome Yazar: Chang, Vivian Y., Federman, Noah, Martinez-Agosto, Julian, Tatishchev, Sergei F., Nelson, Stanley F.

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