Author

Haiguo Wu

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2 Bioinformatics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Assay:whole-genome sequencing· 3 Organism:human· 2 Research Focus:variant calling· 2 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Albarah El-Khani· 2 shared Ayesha Al Ali· 2 shared Azza Attia· 2 shared Fahed Al Marzooqi· 2 shared Gurunath Katagi· 2 shared Javier QuileziD· 2 shared Joseph MafofoiD· 2 shared Judith ArresiD· 2 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Albarah El-Khani

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Author profile →

3 papers

Recent·Most cited

Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications

Judith Arres, Santosh Elavalli, Shalini Behl, Daniel Matías-Sánchez, Ayesha Al Ali, Abdelrahman Ahmed Yehia Abdelaziz Saad, Azza Attia, Cyla Minas, Sharika Pariyachery, Shariq Ahmed, Fatmah Aldhuhoori, Nitu Thulasidharan, Gurunath Katagi, Omar Soliman, Shilp Purohit, , Javier Quilez

This study evaluates Oxford Nanopore sequencing's performance in clinical genomics using reference samples, showing high accuracy for SNVs and SVs but challenges with INDELs and CNVs.

Genome Research · Mar 1, 2026Peer-reviewedGenetic & Genomic Medicine

Pathogenicity Reassessment and Novel Variant Discovery in Inherited Retinal Disease through Population-Scale Genomics in the United Arab Emirates

Budour Alkaf, Wadha Mohammed Abdulrahman, Sahar Al Marzooqi, Daniel Sanchez, Andreas Henschel, Aashish R. Jha, Abdelrahman Saad, Ahmed Al Awadhi, Albarah El-Khani, Aleksander Medvedev, Amna Alsuwaidi, Antonio Milano, Asma Al Mannaei, Ayesha Al Ali, Azza Attia, , Tiago R. Magalhães

The paper reassesses pathogenicity of variants in inherited retinal diseases using population-scale genomics in the UAE, identifying clinically relevant variants and highlighting discrepancies between clinical and population-based classifications.

medRxiv · Oct 14, 2025 · PreprintGenetic & Genomic Medicine

Ultra-fast joint-genotyping with SparkGOR

Hákon Guðbjartsson, Hjalti Þór Ísleifsson, Bergur Ragnarsson, Raony Guimaraes, Haiguo Wu, Hildur Ólafsdóttir, Sigmar K. Stefánsson

This paper introduces SparkGOR, a fast joint-genotyping method that is an order of magnitude faster than existing methods while maintaining high sensitivity and specificity.

bioRxiv · Oct 25, 2022 · PreprintBioinformatics