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Marghoob Mohiyuddin
Marghoob Mohiyuddin
Roche Sequencing Solutions
Dirección de correo verificada de roche.com
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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
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
2612018
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
1162015
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
1082019
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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Artículos 1–20