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Medhat Mahmoud

Showing results (1-10 of 44) with videos related to

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Genome Research|April 14, 2025
A Hitchhiker's Guide to long-read genomic analysisMedhat Mahmoud, Daniel P Agustinho, Fritz J Sedlazeck
Genome Biology|September 15, 2021
PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylationMedhat Mahmoud, Harshavardhan Doddapaneni, Winston Timp, et al.
Genomics|December 23, 2017
Efficiency of PacBio long read correction by 2nd generation Illumina sequencingMedhat Mahmoud, Marek Zywicki, Tomasz Twardowski, et al.
G3 (Bethesda, Md.)|December 1, 2022
Ghat: an R package for identifying adaptive polygenic traitsMedhat Mahmoud, Mila Tost, Ngoc-Thuy Ha, et al.
Genome Biology|October 5, 2023
Genomic variant benchmark: if you cannot measure it, you cannot improve itSina Majidian, Daniel Paiva Agustinho, Chen-Shan Chin, et al.
Plants (Basel, Switzerland)|April 25, 2020
Identification of Structural Variants in Two Novel Genomes of Maize Inbred Lines Possibly Related to Glyphosate ToleranceMedhat Mahmoud, Joanna Gracz-Bernaciak, Marek Żywicki, et al.
Gigascience|September 25, 2021
Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignmentYilei Fu, Medhat Mahmoud, Viginesh Vaibhav Muraliraman, et al.
Nature Communications|March 15, 2022
Rescuing low frequency variants within intra-host viral populations directly from Oxford Nanopore sequencing dataYunxi Liu, Joshua Kearney, Medhat Mahmoud, et al.
Biorxiv : the Preprint Server for Biology|September 14, 2021
Rescuing Low Frequency Variants within Intra-Host Viral Populations directly from Oxford Nanopore sequencing dataYunxi Liu, Joshua Kearney, Medhat Mahmoud, et al.
Genome Biology|November 22, 2019
Structural variant calling: the long and the short of itMedhat Mahmoud, Nastassia Gobet, Diana Ivette Cruz-Dávalos, et al.
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
Genome Research|April 14, 2025
A Hitchhiker's Guide to long-read genomic analysisMedhat Mahmoud, Daniel P Agustinho, Fritz J Sedlazeck
Genome Biology|September 15, 2021
PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylationMedhat Mahmoud, Harshavardhan Doddapaneni, Winston Timp, et al.
Genomics|December 23, 2017
Efficiency of PacBio long read correction by 2nd generation Illumina sequencingMedhat Mahmoud, Marek Zywicki, Tomasz Twardowski, et al.
G3 (Bethesda, Md.)|December 1, 2022
Ghat: an R package for identifying adaptive polygenic traitsMedhat Mahmoud, Mila Tost, Ngoc-Thuy Ha, et al.
Genome Biology|October 5, 2023
Genomic variant benchmark: if you cannot measure it, you cannot improve itSina Majidian, Daniel Paiva Agustinho, Chen-Shan Chin, et al.
Plants (Basel, Switzerland)|April 25, 2020
Identification of Structural Variants in Two Novel Genomes of Maize Inbred Lines Possibly Related to Glyphosate ToleranceMedhat Mahmoud, Joanna Gracz-Bernaciak, Marek Żywicki, et al.
Gigascience|September 25, 2021
Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignmentYilei Fu, Medhat Mahmoud, Viginesh Vaibhav Muraliraman, et al.
Nature Communications|March 15, 2022
Rescuing low frequency variants within intra-host viral populations directly from Oxford Nanopore sequencing dataYunxi Liu, Joshua Kearney, Medhat Mahmoud, et al.
Biorxiv : the Preprint Server for Biology|September 14, 2021
Rescuing Low Frequency Variants within Intra-Host Viral Populations directly from Oxford Nanopore sequencing dataYunxi Liu, Joshua Kearney, Medhat Mahmoud, et al.
Genome Biology|November 22, 2019
Structural variant calling: the long and the short of itMedhat Mahmoud, Nastassia Gobet, Diana Ivette Cruz-Dávalos, et al.
Pageof 5