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Radoje Drmanac

Showing results (1-10 of 47) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 12, 2011
The advent of personal genome sequencingRadoje Drmanac
Nucleic Acids Research|January 30, 2004
Selective DNA amplification from complex genomes using universal double-sided adaptersMatthew J Callow, Snezana Drmanac, Radoje Drmanac
Frontiers in Genetics|February 3, 2015
Co-barcoded sequence reads from long DNA fragments: a cost-effective solution for "perfect genome" sequencingBrock A Peters, Jia Liu, Radoje Drmanac
Methods in Molecular Biology (Clifton, N.J.)|November 6, 2022
A Simple Cost-Effective Method for Whole-Genome Sequencing, Haplotyping, and AssemblyOu Wang, Xiaofang Cheng, Radoje Drmanac, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 1, 2017
Long Fragment Read (LFR) Technology: Cost-Effective, High-Quality Genome-Wide Molecular HaplotypingMark A McElwain, Rebecca Yu Zhang, Radoje Drmanac, et al.
Methods in Molecular Biology (Clifton, N.J.)|November 6, 2022
Large-Scale Complete Sequencing and Haplotyping of 1-10 kb DNA Molecules Using Short Massively Parallel ReadsYoutao Liu, Fei Fan, Radoje Drmanac, et al.
Enzyme and Microbial Technology|September 7, 2021
Reusable and sensitive exonuclease III activity detection on DNB nanoarrays based on cPAS sequencing technologyYing Chen, Hui Wang, Jin Yang, et al.
Peerj|April 2, 2020
IterCluster: a barcode clustering algorithm for long fragment read analysisJiancong Weng, Tian Chen, Yinlong Xie, et al.
Nucleic Acids Research|January 31, 2019
Significant abundance of cis configurations of coding variants in diploid human genomesMargret R Hoehe, Ralf Herwig, Qing Mao, et al.
BMC Genomics|July 25, 2019
Impact of sequencing depth and technology on de novo RNA-Seq assemblyJordan Patterson, Eric J Carpenter, Zhenzhen Zhu, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 12, 2011
The advent of personal genome sequencingRadoje Drmanac
Nucleic Acids Research|January 30, 2004
Selective DNA amplification from complex genomes using universal double-sided adaptersMatthew J Callow, Snezana Drmanac, Radoje Drmanac
Frontiers in Genetics|February 3, 2015
Co-barcoded sequence reads from long DNA fragments: a cost-effective solution for "perfect genome" sequencingBrock A Peters, Jia Liu, Radoje Drmanac
Methods in Molecular Biology (Clifton, N.J.)|November 6, 2022
A Simple Cost-Effective Method for Whole-Genome Sequencing, Haplotyping, and AssemblyOu Wang, Xiaofang Cheng, Radoje Drmanac, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 1, 2017
Long Fragment Read (LFR) Technology: Cost-Effective, High-Quality Genome-Wide Molecular HaplotypingMark A McElwain, Rebecca Yu Zhang, Radoje Drmanac, et al.
Methods in Molecular Biology (Clifton, N.J.)|November 6, 2022
Large-Scale Complete Sequencing and Haplotyping of 1-10 kb DNA Molecules Using Short Massively Parallel ReadsYoutao Liu, Fei Fan, Radoje Drmanac, et al.
Enzyme and Microbial Technology|September 7, 2021
Reusable and sensitive exonuclease III activity detection on DNB nanoarrays based on cPAS sequencing technologyYing Chen, Hui Wang, Jin Yang, et al.
Peerj|April 2, 2020
IterCluster: a barcode clustering algorithm for long fragment read analysisJiancong Weng, Tian Chen, Yinlong Xie, et al.
Nucleic Acids Research|January 31, 2019
Significant abundance of cis configurations of coding variants in diploid human genomesMargret R Hoehe, Ralf Herwig, Qing Mao, et al.
BMC Genomics|July 25, 2019
Impact of sequencing depth and technology on de novo RNA-Seq assemblyJordan Patterson, Eric J Carpenter, Zhenzhen Zhu, et al.
Pageof 5