Resultados da pesquisa - Wendl, Michael C.

Algebraic correction methods for computational assessment of clone overlaps in DNA fingerprint mapping Por Wendl, Michael C

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Extension of Lander-Waterman theory for sequencing filtered DNA libraries Por Wendl, Michael C, Barbazuk, W Brad

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Generalized Gap Model for Bacterial Artificial Chromosome Clone Fingerprint Mapping and Shotgun Sequencing Por Wendl, Michael C., Waterston, Robert H.

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

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

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

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Automated Sequence Preprocessing in a Large-Scale Sequencing Environment Por Wendl, Michael C., Dear, Simon, Hodgson, Dave, Hillier, LaDeana

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Advances for Studying Clonal Evolution in Cancer Por Ding, Li, Raphael, Benjamin J., Chen, Feng, Wendl, Michael C.

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Coverage theories for metagenomic DNA sequencing based on a generalization of Stevens’ theorem Por Wendl, Michael C., Kota, Karthik, Weinstock, George M., Mitreva, Makedonka

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Analysis of next-generation genomic data in cancer: accomplishments and challenges Por Ding, Li, Wendl, Michael C., Koboldt, Daniel C., Mardis, Elaine R.

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Expanding the computational toolbox for mining cancer genomes Por Ding, Li, Wendl, Michael C., McMichael, Joshua F., Raphael, Benjamin J.

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AeQTL: eQTL analysis using region-based aggregation of rare genomic variants Por Dong, Guanlan, Wendl, Michael C., Zhang, Bin, Ding, Li, Huang, Kuan-lin

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PathScan: a tool for discerning mutational significance in groups of putative cancer genes Por 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 Por Wendl, Michael C., Marra, Marco A., Hillier, LaDeana W., Chinwalla, Asif T., Wilson, Richard K., Waterston, Robert H.

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PolyScan: An automatic indel and SNP detection approach to the analysis of human resequencing data Por Chen, Ken, McLellan, Michael D., Ding, Li, Wendl, Michael C., Kasai, Yumi, Wilson, Richard K., Mardis, Elaine R.

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MSIsensor: microsatellite instability detection using paired tumor-normal sequence data Por Niu, Beifang, Ye, Kai, Zhang, Qunyuan, Lu, Charles, Xie, Mingchao, McLellan, Michael D., Wendl, Michael C., Ding, Li

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Codon usage patterns in Nematoda: analysis based on over 25 million codons in thirty-two species Por Mitreva, Makedonka, Wendl, Michael C, Martin, John, Wylie, Todd, Yin, Yong, Larson, Allan, Parkinson, John, Waterston, Robert H, McCarter, James P

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MSIsensor-ct: microsatellite instability detection using cfDNA sequencing data Por Han, Xinyin, Zhang, Shuying, Zhou, Daniel Cui, Wang, Dongliang, He, Xiaoyu, Yuan, Danyang, Li, Ruilin, He, Jiayin, Duan, Xiaohong, Wendl, Michael C, Ding, Li, Niu, Beifang

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BreakPoint Surveyor: a pipeline for structural variant visualization Por Wyczalkowski, Matthew A, Wylie, Kristine M, Cao, Song, McLellan, Michael D, Flynn, Jennifer, Huang, Mo, Ye, Kai, Fan, Xian, Chen, Ken, Wendl, Michael C, Ding, Li

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MuSiC: Identifying mutational significance in cancer genomes Por Dees, Nathan D., Zhang, Qunyuan, Kandoth, Cyriac, Wendl, Michael C., Schierding, William, Koboldt, Daniel C., Mooney, Thomas B., Callaway, Matthew B., Dooling, David, Mardis, Elaine R., Wilson, Richard K., Ding, Li

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