Gabor T. Marth
Affiliations: | Boston College, Newton, MA, United States | ||
| Human Genetics | University of Utah, Salt Lake City, UT |
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Publications
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| Chamberlin JT, Lee Y, Marth G, et al. (2024) Differences in molecular sampling and data processing explain variation among single-cell and single-nucleus RNA-seq experiments. Genome Research |
| Qiao Y, Huang X, Moos PJ, et al. (2024) A Bayesian framework to study tumor subclone-specific expression by combining bulk DNA and single-cell RNA sequencing data. Genome Research |
| Pitman A, Huang X, Marth GT, et al. (2023) quickBAM: a parallelized BAM file access API for high-throughput sequence analysis informatics. Bioinformatics (Oxford, England). 39 |
| Nicholas TJ, Al-Sweel N, Farrell A, et al. (2022) Comprehensive variant calling from whole-genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic hernia. Molecular Genetics & Genomic Medicine. e1888 |
| Ward A, Velinder M, Di Sera T, et al. (2022) : A Collaborative Diagnostic Workflow to Enable Team-Based Precision Genomics. Journal of Personalized Medicine. 12 |
| Di Sera T, Velinder M, Ward A, et al. (2021) Gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritization. Scientific Reports. 11: 20307 |
| Nicholas TJ, Cormier MJ, Huang X, et al. (2021) OncoGEMINI: software for investigating tumor variants from multiple biopsies with integrated cancer annotations. Genome Medicine. 13: 46 |
| Bogenschutz EL, Fox ZD, Farrell A, et al. (2020) Deep whole-genome sequencing of multiple proband tissues and parental blood reveals the complex genetic etiology of congenital diaphragmatic hernias. Hgg Advances. 1 |
| Di Sera T, Velinder M, Ward A, et al. (2020) gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritization. Medrxiv : the Preprint Server For Health Sciences |
| Pedersen BS, Bhetariya PJ, Brown J, et al. (2020) Somalier: rapid relatedness estimation for cancer and germline studies using efficient genome sketches. Genome Medicine. 12: 62 |