Rezultati - Wilson, Richard K

Comparison of Sample Sequences of the Salmonella typhi Genome to the Sequence of the Complete Escherichia coli K-12 Genome od McClelland, Michael, Wilson, Richard K.

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Aspects of coverage in medical DNA sequencing od Wendl, Michael C, Wilson, Richard K

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Statistical aspects of discerning indel-type structural variation via DNA sequence alignment od Wendl, Michael C, Wilson, Richard K

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Cancer genome sequencing: a review od Mardis, Elaine R., Wilson, Richard K.

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The theory of discovering rare variants via DNA sequencing od Wendl, Michael C, Wilson, Richard K

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Chromothripsis and Human Disease: Piecing Together the Shattering Process od Maher, Christopher A., Wilson, Richard K.

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Using SomaticSniper to Detect Somatic Single Nucleotide Variants od Larson, David E., Abbott, Travis E., Wilson, Richard K.

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Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection od Koboldt, Daniel C., Larson, David E., Wilson, Richard K.

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Genomic Landscapes and Clonality of De Novo AML od Miller, Christopher A., Wilson, Richard K., Ley, Timothy J.

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After the Duplication: Gene Loss and Adaptation in Saccharomyces Genomes od Cliften, Paul F., Fulton, Robert S., Wilson, Richard K., Johnston, Mark

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Challenges of sequencing human genomes od Koboldt, Daniel C., Ding, Li, Mardis, Elaine R., Wilson, Richard K.

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Characterizing Ancylostoma caninum transcriptome and exploring nematode parasitic adaptation od Wang, Zhengyuan, Abubucker, Sahar, Martin, John, Wilson, Richard K, Hawdon, John, Mitreva, Makedonka

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Massively Parallel Sequencing Approaches for Characterization of Structural Variation od Koboldt, Daniel C., Larson, David E., Chen, Ken, Ding, Li, Wilson, Richard K.

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Comparing low coverage random shotgun sequence data from Brassica oleracea and Oryza sativa genome sequence for their ability to add to the annotation of Arabidopsis thaliana od Katari, Manpreet S., Balija, Vivekanand, Wilson, Richard K., Martienssen, Robert A., McCombie, W. Richard

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A Transposon-Based Strategy for Sequencing Repetitive DNA in Eukaryotic Genomes od Devine, Scott E., Chissoe, Stephanie L., Eby, Yolanda, Wilson, Richard K., Boeke, Jef D.

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The Next-Generation Sequencing Revolution and Its Impact on Genomics od Koboldt, Daniel C., Steinberg, Karyn Meltz, Larson, David E., Wilson, Richard K., Mardis, Elaine

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Haplotype sorting using human fosmid clone end-sequence pairs od Kidd, Jeffrey M., Cheng, Ze, Graves, Tina, Fulton, Bob, Wilson, Richard K., Eichler, Evan E.

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PathScan: a tool for discerning mutational significance in groups of putative cancer genes od Wendl, Michael C., Wallis, John W., Lin, Ling, Kandoth, Cyriac, Mardis, Elaine R., Wilson, Richard K., Ding, Li

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Theories and Applications for Sequencing Randomly Selected Clones od Wendl, Michael C., Marra, Marco A., Hillier, LaDeana W., Chinwalla, Asif T., Wilson, Richard K., Waterston, Robert H.

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Retrotransposition of gene transcripts leads to structural variation in mammalian genomes od Ewing, Adam D, Ballinger, Tracy J, Earl, Dent, Harris, Christopher C, Ding, Li, Wilson, Richard K, Haussler, David

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