Correction to: IonCRAM: a reference-based compression tool for ion torrent sequence files

by Moustafa Shokrof, Mohamed Abouelhoda
Published 2020-10-01

IonCRAM: a reference-based compression tool for ion torrent sequence files

by Moustafa Shokrof, Mohamed Abouelhoda
Published 2020-09-01

Using the Sadakane Compressed Suffix Tree to Solve the All-Pairs Suffix-Prefix Problem

by Maan Haj Rachid, Qutaibah Malluhi, Mohamed Abouelhoda
Published 2014-01-01

Molecular classification of blood and bleeding disorder genes

by Batoul Baz, Mohamed Abouelhoda, Tarek Owaidah, Majed Dasouki, Dorota Monies, Nada Al Tassan
Published 2021-07-01

Genome sequencing and analysis of the first spontaneous Nanosilver resistant bacterium Proteus mirabilis strain SCDR1

by Amr T. M. Saeb, Khalid A. Al-Rubeaan, Mohamed Abouelhoda, Manojkumar Selvaraju, Hamsa T. Tayeb
Published 2017-11-01

Established and candidate transthyretin amyloidosis variants identified in the Saudi population by data mining

by Mohamed Abouelhoda, Dania Mohty, Islam Alayary, Brian F. Meyer, Stefan T. Arold, Bahaa M. Fadel, Dorota Monies
Published 2021-08-01

High Incidence of Severe Combined Immunodeficiency Disease in Saudi Arabia Detected Through Combined T Cell Receptor Excision Circle and Next Generation Sequencing of Newborn Dried...

by Hamoud Al-Mousa, Hamoud Al-Mousa, Hamoud Al-Mousa, Ghadah Al-Dakheel, Amal Jabr, Fahd Elbadaoui, Mohamed Abouelhoda, Mohamed Abouelhoda, Mansoor Baig, Dorota Monies, Dorota Monies, Brian Meyer, Brian Meyer, Abbas Hawwari, Abbas Hawwari, Majed Dasouki
Published 2018-04-01

Streaming Support for Data Intensive Cloud-Based Sequence Analysis

by Shadi A. Issa, Romeo Kienzler, Mohamed El-Kalioby, Peter J. Tonellato, Dennis Wall, Rémy Bruggmann, Mohamed Abouelhoda
Published 2013-01-01

The Use of Next-Generation Sequencing in the Identification of a Fastidious Pathogen: A Lesson From a Clinical Setup

by Amr TM Saeb, Mohamed Abouelhoda, Manojkumar Selvaraju, Sahar I Althawadi, Maysoon Mutabagani, Mohammad Adil, Abdullah Al Hokail, Hamsa T Tayeb
Published 2017-01-01

Whole-Genome Sequencing Reveals Exonic Variation of ASIC5 Gene Results in Recurrent Pregnancy Loss

by Nourah H. Al Qahtani, Sayed AbdulAzeez, Noor B. Almandil, Norah Fahad Alhur, Hind Saleh Alsuwat, Hatoon Ahmed Al Taifi, Ahlam A. Al-Ghamdi, B. Rabindran Jermy, Mohamed Abouelhoda, Mohamed Abouelhoda, Shazia Subhani, Shazia Subhani, Lubna Al Asoom, J. Francis Borgio, J. Francis Borgio
Published 2021-07-01

Novel CARMIL2 Mutations in Patients with Variable Clinical Dermatitis, Infections, and Combined Immunodeficiency

by Anas M. Alazami, Anas M. Alazami, Maryam Al-Helale, Safa Alhissi, Bandar Al-Saud, Huda Alajlan, Dorota Monies, Dorota Monies, Zeeshan Shah, Zeeshan Shah, Mohamed Abouelhoda, Mohamed Abouelhoda, Rand Arnaout, Rand Arnaout, Hasan Al-Dhekri, Nouf S. Al-Numair, Hazem Ghebeh, Hazem Ghebeh, Farrukh Sheikh, Hamoud Al-Mousa, Hamoud Al-Mousa, Hamoud Al-Mousa
Published 2018-02-01

Unique Features of Germline Variation in Five Egyptian Familial Breast Cancer Families Revealed by Exome Sequencing.

by Yeong C Kim, Amr S Soliman, Jian Cui, Mohamed Ramadan, Ahmed Hablas, Mohamed Abouelhoda, Nehal Hussien, Ola Ahmed, Abdel-Rahman Nabawy Zekri, Ibrahim A Seifeldin, San Ming Wang
Published 2017-01-01

Whole-genome sequencing of human Pegivirus variant from an Egyptian patient co-infected with hepatitis C virus: a case report

by Hany K. Soliman, Mohamed Abouelhoda, Mahmoud N. El Rouby, Ola S. Ahmed, G. Esmat, Zeinab K. Hassan, Mohammed M. Hafez, Dina Ahmed Mehaney, Manojkumar Selvaraju, Rania Kamal Darwish, Yehia A. Osman, Abdel-Rahman N. Zekri
Published 2019-11-01

Targeted next generation sequencing identifies somatic mutations in a cohort of Egyptian breast cancer patients

by Auhood Nassar, Mohamed Abouelhoda, Osman Mansour, Samah A. Loutfy, Mohamed M. Hafez, M. Gomaa, Abeer Bahnassy, Amira Salah El-Din Youssef, Mai M. Lotfy, Hoda Ismail, Ola S. Ahmed, Amany Abd-Elhameed Abou-Bakr, Abdel-Rahman N. Zekri
Published 2020-07-01

Comprehensive multi-omics analysis of G6PC3 deficiency-related congenital neutropenia with inflammatory bowel disease

by Majed Dasouki, Ayodeele Alaiya, Tanziel ElAmin, Zakia Shinwari, Dorota Monies, Mohamed Abouelhoda, Amjad Jabaan, Feras Almourfi, Zuhair Rahbeeni, Fahad Alsohaibani, Fahad Almohareb, Hazzaa Al-Zahrani, Francisco J. Guzmán Vega, Stefan T. Arold, Mahmoud Aljurf, Syed Osman Ahmed
Published 2021-03-01

A novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)-creating mutation

by Nisha Patel, Arif O. Khan, Maher Al-Saif, Walid N. Moghrabi, Balsam M. AlMaarik, Niema Ibrahim, Firdous Abdulwahab, Mais Hashem, Tarfa Alshidi, Eman Alobeid, Rana A. Alomar, Saad Al-Harbi, Mohamed Abouelhoda, Khalid S. A. Khabar, Fowzan S. Alkuraya
Published 2017-07-01

Validation of Ion TorrentTM Inherited Disease Panel with the PGMTM Sequencing Platform for Rapid and Comprehensive Mutation Detection

by Abeer E. Mustafa, Tariq Faquih, Batoul Baz, Rana Kattan, Abdulelah Al-Issa, Asma I. Tahir, Faiqa Imtiaz, Khushnooda Ramzan, Moeenaldeen Al-Sayed, Mohammed Alowain, Zuhair Al-Hassnan, Hamad Al-Zaidan, Mohamed Abouelhoda, Bashayer R. Al-Mubarak, Nada A. Al Tassan
Published 2018-05-01

Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families

by Bashayer Al-Mubarak, Mohamed Abouelhoda, Aisha Omar, Hesham AlDhalaan, Mohammed Aldosari, Michael Nester, Hussain. A. Alshamrani, Mohamed El-Kalioby, Ewa Goljan, Renad Albar, Shazia Subhani, Asma Tahir, Sultana Asfahani, Alaa Eskandrani, Ahmed Almusaiab, Amna Magrashi, Jameela Shinwari, Dorota Monies, Nada Al Tassan
Published 2017-07-01

Genomic characterization of SARS-CoV-2 in Egypt

by Abdel-Rahman N. Zekri, Khaled Easa Amer, Mohammed M. Hafez, Zeinab K. Hassan, Ola S Ahmed, Hany K. Soliman, Abeer A. Bahnasy, Wael Abdel Hamid, Ahmad Gad, Mahmoud Ali, Wael Ali Hassan, Mahmoud Samir Madboly, Ahmad Abdel Raouf, Ayman A. Khattab, Mona Salah El Din Hamdy, May Sherif Soliman, Maha Hamdi El Sissy, Sara Mohamed El khateeb, Moushira Hosny Ezzelarab, Lamiaa A. Fathalla, Mohamed Abouelhoda
Published 2021-05-01

Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families

by Anas M. Alazami, Nisha Patel, Hanan E. Shamseldin, Shamsa Anazi, Mohammed S. Al-Dosari, Fatema Alzahrani, Hadia Hijazi, Muneera Alshammari, Mohammed A. Aldahmesh, Mustafa A. Salih, Eissa Faqeih, Amal Alhashem, Fahad A. Bashiri, Mohammed Al-Owain, Amal Y. Kentab, Sameera Sogaty, Saeed Al Tala, Mohamad-Hani Temsah, Maha Tulbah, Rasha F. Aljelaify, Saad A. Alshahwan, Mohammed Zain Seidahmed, Adnan A. Alhadid, Hesham Aldhalaan, Fatema AlQallaf, Wesam Kurdi, Majid Alfadhel, Zainab Babay, Mohammad Alsogheer, Namik Kaya, Zuhair N. Al-Hassnan, Ghada M.H. Abdel-Salam, Nouriya Al-Sannaa, Fuad Al Mutairi, Heba Y. El Khashab, Saeed Bohlega, Xiaofei Jia, Henry C. Nguyen, Rakad Hammami, Nouran Adly, Jawahir Y. Mohamed, Firdous Abdulwahab, Niema Ibrahim, Ewa A. Naim, Banan Al-Younes, Brian F. Meyer, Mais Hashem, Ranad Shaheen, Yong Xiong, Mohamed Abouelhoda, Abdulrahman A. Aldeeri, Dorota M. Monies, Fowzan S. Alkuraya
Published 2015-01-01