Resultados da pesquisa - Homer, Nils

A survey of sequence alignment algorithms for next-generation sequencing Por Li, Heng, Homer, Nils

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

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

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

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

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RipTide Ultra High-Throughput Rapid DNA Library Preparation for Next Generation Sequencing Por Siddique, Azeem, Suckow, Gaia, Bahena, Jorge, Homer, Nils, Ordoukhanian, Phillip, Head, Steve, Brown, Keith

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Statistical Comparison Framework and Visualization Scheme for Ranking-Based Algorithms in High-Throughput Genome-Wide Studies Por Tembe, Waibhav D., Pearson, John V., Homer, Nils, Lowey, James, Suh, Edward, Craig, David W.

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The Sequence Alignment/Map format and SAMtools Por Li, Heng, Handsaker, Bob, Wysoker, Alec, Fennell, Tim, Ruan, Jue, Homer, Nils, Marth, Gabor, Abecasis, Goncalo, Durbin, Richard

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Multimarker analysis and imputation of multiple platform pooling-based genome-wide association studies Por Homer, Nils, Tembe, Waibhav D., Szelinger, Szabolcs, Redman, Margot, Stephan, Dietrich A., Pearson, John V., Nelson, Stanley F., Craig, David

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U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line Por Clark, Michael James, Homer, Nils, O'Connor, Brian D., Chen, Zugen, Eskin, Ascia, Lee, Hane, Merriman, Barry, Nelson, Stanley F.

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Correction: U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line Por Clark, Michael James, Homer, Nils, O'Connor, Brian D., Chen, Zugen, Eskin, Ascia, Lee, Hane, Merriman, Barry, Nelson, Stanley F.

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RipTide High Throughput NGS Library Prep for Genotyping in Populations Por Siddique, Azeem, Suckow, Gaia, Ordoukhanian, Phillip, Head, Steve, Homer, Nils, Hernandez, Alvaro, Brown, Keith, Glick, Lior, Baruch, Kobi, Doran, Paul

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Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing Por Lee, Hane, O'Connor, Brian D, Merriman, Barry, Funari, Vincent A, Homer, Nils, Chen, Zugen, Cohn, Daniel H, Nelson, Stanley F

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Next Generation Genotyping (NGG) for Population Scale Genomic Studies Using Riptide™ DNA Library Preparation Por Siddique, Azeem, Brown, Keith, Suckow, Gaia, Homer, Nils, Ordoukhanian, Phillip, Head, Steve, Pickrell, Joseph, Kim, Ryan, Ashworth, Roxann, Chittur, Sridar, Kermack, Justin

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Resolving Individuals Contributing Trace Amounts of DNA to Highly Complex Mixtures Using High-Density SNP Genotyping Microarrays Por Homer, Nils, Szelinger, Szabolcs, Redman, Margot, Duggan, David, Tembe, Waibhav, Muehling, Jill, Pearson, John V., Stephan, Dietrich A., Nelson, Stanley F., Craig, David W.

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CRISPR-Mediated Depletion of Ribosomal RNA-Derived DNA from RNA-Seq NGS Libraries Por Siddique, Azeem, Suckow, Gaia, Head, Steve, Ordoukhanian, Phillip, Sussman, Hallie, Ramachandran, Dhanya, Homer, Nils, Bajena, Jorge, Brown, Keith, Chittur, Sridar, Knudtson, Kevin, Kermack, Justin

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Next Generation Genotyping (NGG) Using Riptide™. Performance Specifications when Best Practices are Applied Por Brown, Keith, Siddique, Azeem, Suckow, Gaia, Homer, Nils, Carey, Jay, Ordoukhanian, Phillip, Head, Steve, Pickrell, Joseph, Kim, Ryan, Ashworth, Roxann, Chittur, Sridar, Kermack, Justin

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IDENTIFICATION OF GENETIC VARIANTS USING BARCODED MULTIPLEXED SEQUENCING Por Craig, David W., Pearson, John V., Szelinger, Szabolcs, Sekar, Aswin, Margot, Redma, Corneveaux, Jason J., Pawlowski, Traci L., Laub, Trisha, Nunn, Gary, Stephan, Dietrich A., Homer, Nils, Huentelman, Matthew J.

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A Genome-wide Analysis Identifies Genetic Variants in the RELN Gene Associated with Otosclerosis Por Schrauwen, Isabelle, Ealy, Megan, Huentelman, Matthew J., Thys, Melissa, Homer, Nils, Vanderstraeten, Kathleen, Fransen, Erik, Corneveaux, Jason J., Craig, David W., Claustres, Mireille, Cremers, Cor W.R.J., Dhooge, Ingeborg, Van de Heyning, Paul, Vincent, Robert, Offeciers, Erwin, Smith, Richard J.H., Van Camp, Guy

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Identification of the Genetic Basis for Complex Disorders by Use of Pooling-Based Genomewide Single-Nucleotide–Polymorphism Association Studies Por Pearson, John V., Huentelman, Matthew J., Halperin, Rebecca F., Tembe, Waibhav D., Melquist, Stacey, Homer, Nils, Brun, Marcel, Szelinger, Szabolcs, Coon, Keith D., Zismann, Victoria L., Webster, Jennifer A., Beach, Thomas, Sando, Sigrid B., Aasly, Jan O., Heun, Reinhard, Jessen, Frank, Kölsch, Heike, Tsolaki, Magdalini, Daniilidou, Makrina, Reiman, Eric M., Papassotiropoulos, Andreas, Hutton, Michael L., Stephan, Dietrich A., Craig, David W.

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