Jeremy Leipzig
Affiliations: | Drexel University, Philadelphia, PA, United States |
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BioinformaticsGoogle:
"Jeremy Leipzig"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Gary Earl Duncan | research assistant | 1997-2000 | UNC Chapel Hill |
| Frederic D. Bushman | research assistant | 2004-2007 | University of Pennsylvania School of Medicine (Computational Biology Tree) |
| Steffen Heber | grad student | 2001-2003 | NCSU |
| Jane Greenberg | grad student | 2016-2020 | Drexel |
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Publications
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| Leipzig J, Nüst D, Hoyt CT, et al. (2021) The role of metadata in reproducible computational research. Patterns (New York, N.Y.). 2: 100322 |
| Raman P, Zimmerman S, Rathi KS, et al. (2019) A comparison of survival analysis methods for cancer gene expression RNA-Sequencing data. Cancer Genetics. 235: 1-12 |
| McManus MJ, Picard M, Chen HW, et al. (2018) Mitochondrial DNA Variation Dictates Expressivity and Progression of Nuclear DNA Mutations Causing Cardiomyopathy. Cell Metabolism |
| Sonney S, Leipzig J, Lott MT, et al. (2017) Predicting the pathogenicity of novel variants in mitochondrial tRNA with MitoTIP. Plos Computational Biology. 13: e1005867 |
| Shen L, Diroma MA, Gonzalez M, et al. (2016) MSeqDR: A Centralized Knowledge Repository and Bioinformatics Web Resource to Facilitate Genomic Investigations in Mitochondrial Disease. Human Mutation |
| Falk MJ, Shen L, Gonzalez M, et al. (2015) Mitochondrial Disease Sequence Data Resource (MSeqDR): a global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities. Molecular Genetics and Metabolism. 114: 388-96 |
| Navarro-Gomez D, Leipzig J, Shen L, et al. (2015) Phy-Mer: a novel alignment-free and reference-independent mitochondrial haplogroup classifier. Bioinformatics (Oxford, England). 31: 1310-2 |
| Falk MJ, Shen L, Gonzalez M, et al. (2015) MSeqDR: Making genomics accessible to the mitochondrial disease community Mitochondrion. 24: S2-S3 |
| Zhang Z, Leipzig J, Sasson A, et al. (2013) Efficient digest of high-throughput sequencing data in a reproducible report. Bmc Bioinformatics. 14: S3 |
| Zaidi S, Choi M, Wakimoto H, et al. (2013) De novo mutations in histone-modifying genes in congenital heart disease. Nature. 498: 220-3 |