Michael Lawrence, Ph.D.
Affiliations: | 2008 | Statistics | Iowa State University, Ames, IA, United States |
Google:
"Michael Lawrence"Parents
Sign in to add mentor| Eve S. Wurtele | grad student | 2008 | Iowa State | |
| (Interactive graphics, graphical user interfaces and software interfaces for the analysis of biological experimental data and networks.) | ||||
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Lee S, Lawrence M, Love MI. (2020) Fluent genomics with and . F1000research. 9: 109 |
| Lee S, Cook D, Lawrence M. (2019) plyranges: a grammar of genomic data transformation. Genome Biology. 20: 4 |
| Becker G, Moore SE, Lawrence M. (2019) trackr: A Framework for Enhancing Discoverability and Reproducibility of Data Visualizations and Other Artifacts in R Journal of Computational and Graphical Statistics. 28: 644-658 |
| Zhu LJ, Lawrence M, Gupta A, et al. (2017) GUIDEseq: a bioconductor package to analyze GUIDE-Seq datasets for CRISPR-Cas nucleases. Bmc Genomics. 18: 379 |
| Becker G, Barr C, Gentleman R, et al. (2017) Enhancing reproducibility and collaboration via management of R package cohorts Journal of Statistical Software. 82: 1-18 |
| Goldstein LD, Cao Y, Pau G, et al. (2016) Prediction and Quantification of Splice Events from RNA-Seq Data. Plos One. 11: e0156132 |
| Wu TD, Reeder J, Lawrence M, et al. (2016) GMAP and GSNAP for Genomic Sequence Alignment: Enhancements to Speed, Accuracy, and Functionality. Methods in Molecular Biology (Clifton, N.J.). 1418: 283-334 |
| Giannakis M, Mu JX, Shukla S, et al. (2016) Novel driver genes and genomic predictors of immune infiltrates in colorectal cancer. Journal of Clinical Oncology. 34: 557-557 |
| Landau DA, Tausch E, Taylor-Weiner AN, et al. (2015) Mutations driving CLL and their evolution in progression and relapse. Nature. 526: 525-30 |
| Gehring JS, Fischer B, Lawrence M, et al. (2015) SomaticSignatures: inferring mutational signatures from single-nucleotide variants. Bioinformatics (Oxford, England) |