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Marghoob Mohiyuddin

Showing results (1-10 of 23) with videos related to

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Scientific Reports|March 20, 2020
ecTMB: a robust method to estimate and classify tumor mutational burdenLijing Yao, Yao Fu, Marghoob Mohiyuddin, et al.
Bioinformatics (Oxford, England)|July 20, 2012
Fast and accurate read alignment for resequencingJohn C Mu, Hui Jiang, Amirhossein Kiani, et al.
Nature Communications|March 6, 2019
Deep convolutional neural networks for accurate somatic mutation detectionSayed Mohammad Ebrahim Sahraeian, Ruolin Liu, Bayo Lau, et al.
Computational and Structural Biotechnology Journal|July 5, 2022
Targeted removal of mitochondrial DNA from mouse and human extrachromosomal circular DNA with CRISPR-Cas9Weijia Feng, Gerard Arrey, Egija Zole, et al.
Bioinformatics (Oxford, England)|September 27, 2016
LongISLND: in silico sequencing of lengthy and noisy datatypesBayo Lau, Marghoob Mohiyuddin, John C Mu, et al.
Bioinformatics (Oxford, England)|December 20, 2014
VarSim: a high-fidelity simulation and validation framework for high-throughput genome sequencing with cancer applicationsJohn C Mu, Marghoob Mohiyuddin, Jian Li, et al.
Bioinformatics (Oxford, England)|April 12, 2015
MetaSV: an accurate and integrative structural-variant caller for next generation sequencingMarghoob Mohiyuddin, John C Mu, Jian Li, et al.
Cancer Medicine|August 21, 2023
Methods for the purification and detection of single nucleotide KRAS mutations on extrachromosomal circular DNA in human plasmaLasse Bøllehuus Hansen, Sandra Fugl Jakobsen, Egija Zole, et al.
BMC Genomics|January 17, 2016
svclassify: a method to establish benchmark structural variant callsHemang Parikh, Marghoob Mohiyuddin, Hugo Y K Lam, et al.
Scientific Reports|September 29, 2015
Leveraging long read sequencing from a single individual to provide a comprehensive resource for benchmarking variant calling methodsJohn C Mu, Pegah Tootoonchi Afshar, Marghoob Mohiyuddin, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Scientific Reports|March 20, 2020
ecTMB: a robust method to estimate and classify tumor mutational burdenLijing Yao, Yao Fu, Marghoob Mohiyuddin, et al.
Bioinformatics (Oxford, England)|July 20, 2012
Fast and accurate read alignment for resequencingJohn C Mu, Hui Jiang, Amirhossein Kiani, et al.
Nature Communications|March 6, 2019
Deep convolutional neural networks for accurate somatic mutation detectionSayed Mohammad Ebrahim Sahraeian, Ruolin Liu, Bayo Lau, et al.
Computational and Structural Biotechnology Journal|July 5, 2022
Targeted removal of mitochondrial DNA from mouse and human extrachromosomal circular DNA with CRISPR-Cas9Weijia Feng, Gerard Arrey, Egija Zole, et al.
Bioinformatics (Oxford, England)|September 27, 2016
LongISLND: in silico sequencing of lengthy and noisy datatypesBayo Lau, Marghoob Mohiyuddin, John C Mu, et al.
Bioinformatics (Oxford, England)|December 20, 2014
VarSim: a high-fidelity simulation and validation framework for high-throughput genome sequencing with cancer applicationsJohn C Mu, Marghoob Mohiyuddin, Jian Li, et al.
Bioinformatics (Oxford, England)|April 12, 2015
MetaSV: an accurate and integrative structural-variant caller for next generation sequencingMarghoob Mohiyuddin, John C Mu, Jian Li, et al.
Cancer Medicine|August 21, 2023
Methods for the purification and detection of single nucleotide KRAS mutations on extrachromosomal circular DNA in human plasmaLasse Bøllehuus Hansen, Sandra Fugl Jakobsen, Egija Zole, et al.
BMC Genomics|January 17, 2016
svclassify: a method to establish benchmark structural variant callsHemang Parikh, Marghoob Mohiyuddin, Hugo Y K Lam, et al.
Scientific Reports|September 29, 2015
Leveraging long read sequencing from a single individual to provide a comprehensive resource for benchmarking variant calling methodsJohn C Mu, Pegah Tootoonchi Afshar, Marghoob Mohiyuddin, et al.
Pageof 3