Tavaxy: Integrating Taverna and Galaxy workflows with cloud computing support

Por Abouelhoda Mohamed, Issa Shadi, Ghanem Moustafa
Publicado em 2012-05-01

A fast algorithm for the multiple genome rearrangement problem with weighted reversals and transpositions

Por Bader, Martin, Abouelhoda, Mohamed I, Ohlebusch, Enno
Publicado em 2008

WAMI: a web server for the analysis of minisatellite maps

Por Abouelhoda, Mohamed, El-Kalioby, Mohamed, Giegerich, Robert
Publicado em 2010

CoCoNUT: an efficient system for the comparison and analysis of genomes

Por Abouelhoda, Mohamed I, Kurtz, Stefan, Ohlebusch, Enno
Publicado em 2008

Tavaxy: Integrating Taverna and Galaxy workflows with cloud computing support

Por Abouelhoda, Mohamed, Issa, Shadi Alaa, Ghanem, Moustafa
Publicado em 2012

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

Por Haj Rachid, Maan, Malluhi, Qutaibah, Abouelhoda, Mohamed
Publicado em 2014

A hybrid method for the exact planted (l, d) motif finding problem and its parallelization

Por Abbas, Mostafa M, Abouelhoda, Mohamed, Bahig, Hazem M
Publicado em 2012

Revisiting the morbid genome of Mendelian disorders

Por Abouelhoda, Mohamed, Faquih, Tariq, El-Kalioby, Mohamed, Alkuraya, Fowzan S.
Publicado no Genome Biol (2016)

MC-GenomeKey: a multicloud system for the detection and annotation of genomic variants

Por Elshazly, Hatem, Souilmi, Yassine, Tonellato, Peter J., Wall, Dennis P., Abouelhoda, Mohamed
Publicado no BMC Bioinformatics (2017)

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

Por Saeb, Amr T. M., Al-Rubeaan, Khalid A., Abouelhoda, Mohamed, Selvaraju, Manojkumar, Tayeb, Hamsa T.
Publicado no Antimicrob Resist Infect Control (2017)

Personalized cloud-based bioinformatics services for research and education: use cases and the elasticHPC package

Por El-Kalioby, Mohamed, Abouelhoda, Mohamed, Krüger, Jan, Giegerich, Robert, Sczyrba, Alexander, Wall, Dennis P, Tonellato, Peter
Publicado em 2012

Streaming Support for Data Intensive Cloud-Based Sequence Analysis

Por Issa, Shadi A., Kienzler, Romeo, El-Kalioby, Mohamed, Tonellato, Peter J., Wall, Dennis, Bruggmann, Rémy, Abouelhoda, Mohamed
Publicado em 2013

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

Por Saeb, Amr TM, Abouelhoda, Mohamed, Selvaraju, Manojkumar, Althawadi, Sahar I, Mutabagani, Maysoon, Adil, Mohammad, Al Hokail, Abdullah, Tayeb, Hamsa T
Publicado no Evol Bioinform Online (2017)

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...

Por Al-Mousa, Hamoud, Al-Dakheel, Ghadah, Jabr, Amal, Elbadaoui, Fahd, Abouelhoda, Mohamed, Baig, Mansoor, Monies, Dorota, Meyer, Brian, Hawwari, Abbas, Dasouki, Majed
Publicado no Front Immunol (2018)

New insight into HCV E1/E2 region of genotype 4a

Por Hussein, Nehal, Zekri, Abdel-Rahman N, Abouelhoda, Mohamed, Alam El-din, Hanaa M, Ghamry, Ahmed Abdelwahab, Amer, Mahmoud A, sherif, Ghada M, Bahnassy, Abeer A
Publicado no Virol J (2014)

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

Por Kim, Yeong C., Soliman, Amr S., Cui, Jian, Ramadan, Mohamed, Hablas, Ahmed, Abouelhoda, Mohamed, Hussien, Nehal, Ahmed, Ola, Zekri, Abdel-Rahman Nabawy, Seifeldin, Ibrahim A., Wang, San Ming
Publicado no PLoS One (2017)

Early detection of hepatocellular carcinoma co-occurring with hepatitis C virus infection: A mathematical model

Por Zekri, Abdel-Rahman Nabawy, Youssef, Amira Salah El-Din, Bakr, Yasser Mabrouk, Gabr, Reham Mohamed, Ahmed, Ola Sayed, Elberry, Mostafa Hamed, Mayla, Ahmed Mahmoud, Abouelhoda, Mohamed, Bahnassy, Abeer A
Publicado no World J Gastroenterol (2016)

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

Por Alazami, Anas M., Al-Helale, Maryam, Alhissi, Safa, Al-Saud, Bandar, Alajlan, Huda, Monies, Dorota, Shah, Zeeshan, Abouelhoda, Mohamed, Arnaout, Rand, Al-Dhekri, Hasan, Al-Numair, Nouf S., Ghebeh, Hazem, Sheikh, Farrukh, Al-Mousa, Hamoud
Publicado no Front Immunol (2018)

Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and Mice

Por Shaheen, Ranad, Anazi, Shams, Ben-Omran, Tawfeg, Seidahmed, Mohammed Zain, Caddle, L. Brianna, Palmer, Kristina, Ali, Rehab, Alshidi, Tarfa, Hagos, Samya, Goodwin, Leslie, Hashem, Mais, Wakil, Salma M., Abouelhoda, Mohamed, Colak, Dilek, Murray, Stephen A., Alkuraya, Fowzan S.
Publicado no Am J Hum Genet (2016)

Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families

Por Bohlega, Saeed A., Al-Mubarak, Bashayer R., Alyemni, Eman A., Abouelhoda, Mohamed, Monies, Dorota, Mustafa, Abeer E., Khalil, Dania S., Al Haibi, Sara, Abou Al-Shaar, Hussam, Faquih, Tariq, El-Kalioby, Mohamed, Tahir, Asma I., Al Tassan, Nada A.
Publicado no BMC Res Notes (2016)