Mark A. Umbarger, Ph.D.
Affiliations: | 2010 | Harvard University, Cambridge, MA, United States |
Area:
Computational GeneticsGoogle:
"Mark Umbarger"Mean distance: 9.43 | S | N | B | C | P |
Parents
Sign in to add mentor| George M. Church | grad student | 2010 | Harvard | |
| (New tools to probe bacterial chromosome folding.) | ||||
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Publications
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| Kosheleva K, Velenich A, Sartain C, et al. (2018) Validation of a next generation sequencing-based preimplantation genetic screening assay for the calling of triploidy and uniparental isodisomy Fertility and Sterility. 109: e54 |
| Umbarger M, Boyden E, Faulkner N, et al. (2017) Targeted next generation sequencing-based pgs can enable detection of uniparental isodisomy, familial relationships, and polyploidy Fertility and Sterility. 108: e270 |
| Zhu M, Neitzel D, Umbarger M, et al. (2017) Identification of polyploid embryos using a targeted NGS-based preimplantation genetic screening assay Fertility and Sterility. 108: e269 |
| Umbarger M, Germain K, Gore A, et al. (2016) Accurate detection of segmental aneuploidy in preimplantation genetic screening using targeted next-generation DNA sequencing Fertility and Sterility. 106: e152 |
| Gole J, Mullen T, Celia G, et al. (2016) Analytical validation of a novel next-generation sequencing based preimplantation genetic screening technology Fertility and Sterility. 105: e25 |
| Hallam S, Nelson H, Greger V, et al. (2014) Validation for clinical use of, and initial clinical experience with, a novel approach to population-based carrier screening using high-throughput, next-generation DNA sequencing. The Journal of Molecular Diagnostics : Jmd. 16: 180-9 |
| Umbarger MA, Kennedy CJ, Saunders P, et al. (2014) Next-generation carrier screening. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 132-40 |
| Porreca G, Gole J, Gore A, et al. (2014) Adapting next-generation DNA sequencing to detect aneuploidy Fertility and Sterility. 102: e181-e182 |
| Hoffman JD, Greger V, Strovel ET, et al. (2013) Next-generation DNA sequencing of HEXA: a step in the right direction for carrier screening. Molecular Genetics & Genomic Medicine. 1: 260-8 |
| Hallam S, Breton B, Faulkner N, et al. (2013) Carrier Screening for Cystic Fibrosis among IVF Patients Utilizing Next Generation DNA Sequencing Detects Common, Rare, and Otherwise Undetectable Mutations Fertility and Sterility. 99: S35 |