Batsal Devkota, Ph.D.
Affiliations: | 2008 | Georgia Institute of Technology, Atlanta, GA |
Area:
Molecular Biology, Bioinformatics BiologyGoogle:
"Batsal Devkota"Mean distance: (not calculated yet)
Cross-listing: Computational Biology Tree
Parents
Sign in to add mentor| Stephen C. Harvey | grad student | 2008 | Georgia Tech | |
| (Structural studies of ribonucleoprotein complexes using molecular modeling.) | ||||
| Deanne Marie Taylor | research scientist | Children’s Hospital of Philadelphia / University of Pennsylvania | ||
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Publications
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| Mandl KD, Glauser T, Krantz ID, et al. (2019) Correction: The Genomics Research and Innovation Network: creating an interoperable, federated, genomics learning system. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Mandl KD, Glauser T, Krantz ID, et al. (2019) The Genomics Research and Innovation Network: creating an interoperable, federated, genomics learning system. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Taylor DM, Aronow BJ, Tan K, et al. (2019) The Pediatric Cell Atlas: Defining the Growth Phase of Human Development at Single-Cell Resolution. Developmental Cell |
| Wu C, Devkota B, Evans P, et al. (2019) Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approach. European Journal of Human Genetics : Ejhg |
| Zhu Y, Brown M, Devkota B, et al. (2019) Abstract 2465: Genomic harmonization of the Data Resource Center for Gabriella Miller Kids First Pediatric Research Program Cancer Research |
| Romasko EJ, Devkota B, Biswas S, et al. (2017) Utility and limitations of exome sequencing in the molecular diagnosis of pediatric inherited platelet disorders. American Journal of Hematology |
| Romasko EJ, Biswas S, Devkota B, et al. (2016) Utility of Whole Exome Sequencing in Diagnosis of Pediatric Platelet Disorders: A Subanalysis of the Pediseq Study Blood. 128: 3726-3726 |
| Rajagopalan R, Devkota B, Jayaraman V, et al. (2016) Copy Number Detection in Exome Sequencing Compared to Chromosomal Microarray in a Clinical Setting Cancer Genetics. 209: 300 |
| Fedick AM, Eckert K, Thompson K, et al. (2014) Lack of association of KATNAL1 gene sequence variants and azoospermia in humans. Journal of Assisted Reproduction and Genetics. 31: 1065-71 |
| Gueye NA, Devkota B, Taylor D, et al. (2014) Uniparental disomy in the human blastocyst is exceedingly rare. Fertility and Sterility. 101: 232-6 |