Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mohammed O E Abdallah"'
Autor:
Suleiman H Suleiman, Mahmoud E Koko, Wafaa H Nasir, Ommnyiah eElfateh, Ubai K Elgizouli, Mohammed O E Abdallah, Khalid O Alfarouk, Ayman eHussain, Shima eFaisal, Fathelrahman M A Ibrahim, Maurizio eRomano, Ali eSultan, Lawrence eBanks, Melanie eNewport, Francesco eBaralle, Ahmed M Elhassan, Hiba S Mohamed, Muntaser E Ibrahim
Publikováno v:
Frontiers in Genetics, Vol 6 (2015)
The molecular basis of cancer and cancer multiple phenotypes are not yet fully understood. Next Generation Sequencing promises new insight into the role of genetic interactions in shaping the complexity of cancer. Aiming to outline the differences in
Externí odkaz:
https://doaj.org/article/beba378d14da4031b6b1c66fc3233a2b
Background:The GRCh37 human genome assembly is still widely used in genomics despite the fact an updated human genome assembly (GRCh38) has been available for many years. A particular issue with relevant ramifications for clinical genetics currently
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be367bd2b036815c21fe13f00fce0b76
https://doi.org/10.21203/rs.3.rs-131927/v1
https://doi.org/10.21203/rs.3.rs-131927/v1
Autor:
Clive M. Gray, Alltalents T. Murahwa, Michelle De Sousa, Ramadhani Salum Chambuso, Evelyn Kaambo, Raj Ramesar, Anna-Lise Williamson, Lynette Denny, Mohammed O E Abdallah
Publikováno v:
Medicine
Supplemental Digital Content is available in the text
A subgroup of women who are co-infected with human immunodeficiency virus type 1 (HIV-1) and human papillomavirus (HPV), progress rapidly to cervical disease. We characterized HPV genotypes w
A subgroup of women who are co-infected with human immunodeficiency virus type 1 (HIV-1) and human papillomavirus (HPV), progress rapidly to cervical disease. We characterized HPV genotypes w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f89dcba6305f4fc7d550544878c3d123
https://pubmed.ncbi.nlm.nih.gov/32118737
https://pubmed.ncbi.nlm.nih.gov/32118737
BackgroundLeber Congenital Amaurosis (LCA) is a clinically and genetically heterogeneous inherited retinal dystrophy characterized by early onset visual impairment caused by mutations in not less than 17 genes.AIPL1mutations cause LCA type 4, compris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77a16c21b72e061ad91b961208a24c39
https://doi.org/10.1101/290650
https://doi.org/10.1101/290650
Publikováno v:
BMC Genomics, Vol 19, Iss 1, Pp 1-8 (2018)
BMC Genomics
BMC Genomics
Background The conventional variant calling of pathogenic alleles in exome and genome sequencing requires the presence of the non-pathogenic alleles as genome references. This hinders the correct identification of variants with minor and/or pathogeni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e905b6123960c4030b706eabd22a150
https://doi.org/10.1186/s12864-018-4433-3
https://doi.org/10.1186/s12864-018-4433-3
In variation sites with minor reference alleles, overlooking the detection of homozygous reference genotypes results in inadequate identification of potential disease variants. Current variant calling practices miss these clinically relevant alleles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9114de7e1c47c72acb4fd5039ca46a97
https://doi.org/10.1101/093450
https://doi.org/10.1101/093450
Autor:
Mohammed O E Abdallah, Ahmed M. Elhassan, JH Shakir, Ghimja Fessahaye, Hiba S. Mohamed, UK Algizouli, Meie Ibrahim, Marwa Abd Elmonem Suliman, RA Abdulrahman, Mahmoud Koko, Ahmed H. Fahal
Background Breast cancer (BC) ranks among the most common cancers in Sudan and worldwide with hefty toll on female health and human resources. Recent studies have uncovered a common BC signature characterized by low frequency of oncogenic mutations a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba53203dd2f51044a286666aef6cf07e
https://doi.org/10.1101/034322
https://doi.org/10.1101/034322
Publikováno v:
BMC Genomics, Vol 19, Iss 1, Pp 1-8 (2018)
Abstract Background The conventional variant calling of pathogenic alleles in exome and genome sequencing requires the presence of the non-pathogenic alleles as genome references. This hinders the correct identification of variants with minor and/or
Externí odkaz:
https://doaj.org/article/8a77779fd7f94aaf9c419c7a9ec53cf7