Marghoob Mohiyuddin, Ph.D.

Affiliations: 
2012 Electrical Engineering & Computer Sciences University of California, Berkeley, Berkeley, CA, United States 
Area:
Computer Architecture & Engineering (ARC)
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"Marghoob Mohiyuddin"

Parents

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John Wawrzynek grad student 2012 UC Berkeley
 (Tuning Hardware and Software for Multiprocessors.)
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Publications

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Olson ND, Wagner J, McDaniel J, et al. (2022) PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions. Cell Genomics. 2
Fang LT, Zhu B, Zhao Y, et al. (2021) Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing. Nature Biotechnology. 39: 1151-1160
Li J, Niu L, Greene N, et al. (2020) Ephesus: A curation workflow tool for the clinical interpretation of genomic variants. Journal of Clinical Oncology. 38
Fuentes RR, Chebotarov D, Duitama J, et al. (2019) Structural variants in 3000 rice genomes. Genome Research
Sahraeian SME, Liu R, Lau B, et al. (2019) Deep convolutional neural networks for accurate somatic mutation detection. Nature Communications. 10: 1041
Yao L, Mohiyuddin M, Lam H. (2019) Abstract LB-213: ecTMB: A robust method to estimate and classify tumor mutational burden Cancer Research. 79
Fang LT, Mohiyuddin M, Fu Y, et al. (2017) Abstract 386: OnkoInsight: an end-to-end cancer informatics pipeline to generate insights from large sequencing datasets Cancer Research. 77: 386-386
Lau B, Mohiyuddin M, Mu JC, et al. (2016) LongISLND: In silico Sequencing of Lengthy and Noisy Datatypes. Bioinformatics (Oxford, England)
Parikh H, Mohiyuddin M, Lam HY, et al. (2016) svclassify: a method to establish benchmark structural variant calls. Bmc Genomics. 17: 64
Mu JC, Tootoonchi Afshar P, Mohiyuddin M, et al. (2015) Leveraging long read sequencing from a single individual to provide a comprehensive resource for benchmarking variant calling methods. Scientific Reports. 5: 14493
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