Resultats de la cerca - Homer, Nils

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet

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

Obtenir text complet Obtenir text complet Obtenir text complet

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

Obtenir text complet

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

Obtenir text complet

IDENTIFICATION OF GENETIC VARIANTS USING BARCODED MULTIPLEXED SEQUENCING per 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.

Obtenir text complet Obtenir text complet Obtenir text complet

A Genome-wide Analysis Identifies Genetic Variants in the RELN Gene Associated with Otosclerosis per 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

Obtenir text complet Obtenir text complet Obtenir text complet

Identification of the Genetic Basis for Complex Disorders by Use of Pooling-Based Genomewide Single-Nucleotide–Polymorphism Association Studies per 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.

Obtenir text complet Obtenir text complet