Matthew Snyder
Affiliations: | Genome Sciences | University of Washington, Seattle, Seattle, WA |
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"Matthew Snyder"
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| Kumar RD, Saba LF, Streff H, et al. (2023) Clinical genome sequencing: three years' experience at a tertiary children's hospital. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100916 |
| Farhat MR, Freschi L, Calderon R, et al. (2019) GWAS for quantitative resistance phenotypes in Mycobacterium tuberculosis reveals resistance genes and regulatory regions. Nature Communications. 10: 2128 |
| Shendure J, Findlay GM, Snyder MW. (2019) Genomic Medicine-Progress, Pitfalls, and Promise. Cell. 177: 45-57 |
| Sanchez C, Snyder MW, Tanos R, et al. (2018) New insights into structural features and optimal detection of circulating tumor DNA determined by single-strand DNA analysis. Npj Genomic Medicine. 3: 31 |
| Allix-Béguec C, Arandjelovic I, et al. (2018) Prediction of Susceptibility to First-Line Tuberculosis Drugs by DNA Sequencing. The New England Journal of Medicine. 379: 1403-1415 |
| Zhang Q, Zeng X, Younkin S, et al. (2016) Systematic evaluation of the impact of ChIP-seq read designs on genome coverage, peak identification, and allele-specific binding detection. Bmc Bioinformatics. 17: 96 |
| Snyder MW, Kircher M, Hill AJ, et al. (2016) Cell-free DNA Comprises an In Vivo Nucleosome Footprint that Informs Its Tissues-Of-Origin. Cell. 164: 57-68 |
| Snyder MW, Kircher M, Hill AJ, et al. (2016) Cell-free DNA comprises an in vivo nucleosome footprint that informs its tissues-of-origin Transplantation. 100: 698 |
| Snyder MW, Gammill HS, Shendure J. (2015) Copy-Number Variation and False Positive Results of Prenatal Screening. The New England Journal of Medicine. 373: 2585 |
| Dewey FE, Grove ME, Priest JR, et al. (2015) Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data. Plos Genetics. 11: e1005496 |