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Marghoob Mohiyuddin
Marghoob Mohiyuddin
Roche Sequencing Solutions
Verified email at roche.com
Title
Cited by
Cited by
Year
Circular DNA elements of chromosomal origin are common in healthy human somatic tissue
HD Møller, M Mohiyuddin, I Prada-Luengo, MR Sailani, JF Halling, ...
Nature communications 9 (1), 1069, 2018
2622018
Gaining comprehensive biological insight into the transcriptome by performing a broad-spectrum RNA-seq analysis
SME Sahraeian, M Mohiyuddin, R Sebra, H Tilgner, PT Afshar, KF Au, ...
Nature communications 8 (1), 59, 2017
2622017
Minimizing communication in sparse matrix solvers
M Mohiyuddin, M Hoemmen, J Demmel, K Yelick
Proceedings of the Conference on High Performance Computing Networking …, 2009
1902009
Avoiding communication in sparse matrix computations
J Demmel, M Hoemmen, M Mohiyuddin, K Yelick
2008 IEEE International Symposium on Parallel and Distributed Processing, 1-12, 2008
1852008
MetaSV: an accurate and integrative structural-variant caller for next generation sequencing
M Mohiyuddin, JC Mu, J Li, N Bani Asadi, MB Gerstein, A Abyzov, ...
Bioinformatics 31 (16), 2741-2744, 2015
1542015
Structural variants in 3000 rice genomes
RR Fuentes, D Chebotarov, J Duitama, S Smith, JF De la Hoz, ...
Genome research 29 (5), 870-880, 2019
1252019
An ensemble approach to accurately detect somatic mutations using SomaticSeq
LT Fang, PT Afshar, A Chhibber, M Mohiyuddin, Y Fan, JC Mu, G Gibeling, ...
Genome biology 16, 1-13, 2015
1172015
PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions
ND Olson, J Wagner, J McDaniel, SH Stephens, ST Westreich, ...
Cell genomics 2 (5), 2022
1152022
Deep convolutional neural networks for accurate somatic mutation detection
SME Sahraeian, R Liu, B Lau, K Podesta, M Mohiyuddin, HYK Lam
Nature communications 10 (1), 1041, 2019
1092019
Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms
A Abyzov, S Li, DR Kim, M Mohiyuddin, AM Stütz, NF Parrish, XJ Mu, ...
Nature communications 6 (1), 7256, 2015
922015
Analysis of photonic networks for a chip multiprocessor using scientific applications
G Hendry, S Kamil, A Biberman, J Chan, BG Lee, M Mohiyuddin, A Jain, ...
2009 3rd ACM/IEEE International Symposium on Networks-on-Chip, 104-113, 2009
892009
svclassify: a method to establish benchmark structural variant calls
H Parikh, M Mohiyuddin, HYK Lam, H Iyer, D Chen, M Pratt, G Bartha, ...
BMC genomics 17, 1-16, 2016
872016
Energy-efficient computing for extreme-scale science
D Donofrio, L Oliker, J Shalf, MF Wehner, C Rowen, J Krueger, S Kamil, ...
Computer 42 (11), 62-71, 2009
812009
VarSim: a high-fidelity simulation and validation framework for high-throughput genome sequencing with cancer applications
JC Mu, M Mohiyuddin, J Li, N Bani Asadi, MB Gerstein, A Abyzov, ...
Bioinformatics 31 (9), 1469-1471, 2015
732015
Fast and accurate read alignment for resequencing
JC Mu, H Jiang, A Kiani, M Mohiyuddin, N Bani Asadi, WH Wong
Bioinformatics 28 (18), 2366-2373, 2012
732012
Hardware/software co-design for energy-efficient seismic modeling
J Krueger, D Donofrio, J Shalf, M Mohiyuddin, S Williams, L Oliker, ...
Proceedings of 2011 International Conference for High Performance Computing …, 2011
652011
Systems and methods for processing nucleic acid sequence data
NB Asadi, J Chong, H Chen, M Mohiyuddin, A Doupnik
US Patent 9,600,625, 2017
582017
Avoiding communication in computing Krylov subspaces
J Demmel, M Hoemmen, M Mohiyuddin, K Yelick
EECS Dept., UC Berkeley, Tech. Rep. UCB/EECS-2007-123, 2007
512007
Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
LT Fang, B Zhu, Y Zhao, W Chen, Z Yang, L Kerrigan, K Langenbach, ...
Nature biotechnology 39 (9), 1151-1160, 2021
432021
A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequency
W Jones, B Gong, N Novoradovskaya, D Li, R Kusko, TA Richmond, ...
Genome biology 22, 1-38, 2021
302021
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