Author

Muntaser Eltayeb Ibrahim

University of KhartoumORCID 0000-0003-2242-2143Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 2 Bioinformatics· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 4 Research Focus:variant effect prediction· 3 Assay:DNA methylation· 2 Organism:human· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:genome assembly· 1

Frequent Co-Authors

Mahmoud KokoiD· 2 shared Mohammed O. E. AbdallahiD· 2 shared Asma Ali Hassan AliiD· 1 shared Daniel KeppleiD· 1 shared Eugenia Y. Y. LoiD· 1 shared Eyoab Iyasu GebremeskeliD· 1 shared Melanie J. NewportiD· 1 shared Musab M. Ali AlbsheeriD· 1 shared

Activity by Year

2018-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 15 mutual co-author links

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2 shared papersGenomics

Mahmoud KokoORCID

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4 papers

Recent·Most cited

BioinformaticsbioRxivPreprintNov 14, 2020

In silico analysis of single nucleotide polymorphisms (SNPs) in human C-C chemokine receptor type five (CCR5) gene

Asma Ali Hassan Ali, Muntaser Eltayeb Ibrahim

The paper analyzes SNPs in the CCR5 gene to assess their impact on protein structure and function, identifying deleterious variants associated with HIV resistance.

DOI 10.1101/2020.11.14.382739

humanDNA methylation

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GeneticsbioRxivPreprintJun 1, 2020

Extensive genetic diversity in Plasmodium vivax from Sudan and its genetic relationships with other geographical isolates

Musab M. Ali Albsheer, Eyoab Iyasu Gebremeskel, Daniel Kepple…·Muzamil Mahdi Abdel Hamid

This study analyzes genetic diversity and relationships of Plasmodium vivax isolates from Sudan using microsatellite markers, revealing high diversity and potential recent introductions from Asia.

2 citations

virusDNA methylation

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GenomicsbioRxivPreprintMar 28, 2018

Recurrent AIPL1 c.487C>T truncating variant in Leber Congenital Amaurosis: Support of pathogenicity and regional implications

Mohammed O. E. Abdallah, Mahmoud Koko, Shima Faisal…·Muntaser Eltayeb Ibrahim

The paper reports a recurrent AIPL1 truncating variant in a Sudanese family with Leber Congenital Amaurosis, supporting its pathogenicity and regional significance.

DOI 10.1101/290650

humanwhole-exome sequencing

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GenomicsBMC GenomicsPeer-reviewedJan 15, 2018

A bioinformatic panel to interrogate thousands of ExAC variants with minor reference allele that are missed by conventional variant calling

Mahmoud Koko, Mohammed O. E. Abdallah, Mutaz Amin, Muntaser Eltayeb Ibrahim

The paper develops a bioinformatic panel to identify disease-causing variants missed by conventional variant calling in sites with minor reference alleles.

17 citations

whole-exome sequencingstatistical model

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