检索结果 - Wendl, Michael C

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

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

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

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

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

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

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

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Advances for Studying Clonal Evolution in Cancer 由 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 由 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 由 Ding, Li, Wendl, Michael C., Koboldt, Daniel C., Mardis, Elaine R.

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Expanding the computational toolbox for mining cancer genomes 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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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