Author

Ali Crawford

Illumina (United States)ORCID 0009-0003-2852-624XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Approach:experimental assay· 1 Approach:statistical model· 1

Frequent Co-Authors

Qing ZhangiD· 2 shared Claudia M.B. CarvalhoiD· 1 shared Daniel G. CalameiD· 1 shared Donna Marie MuznyiD· 1 shared Fritz Joachim SedlazeckiD· 1 shared Heer Hemant MehtaiD· 1 shared Huyen DinhiD· 1 shared Jacqueline Weir· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Qing ZhangORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintFeb 4, 2026

Scaling haplospecific antisense oligonucleotides from N-of-1 to broad use in genetic disease populations by diplotyping

Olivia Kim McManus, Pagé C. Goddard, Shahad Olsson…·Stephen Francis Kingsmore

The paper identifies haplospecific antisense oligonucleotides for genetic disorder treatment using population genome sequencing and haplotyping.

DOI 10.64898/2026.01.28.26345012

humanwhole-genome sequencing

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Genetic & Genomic MedicinemedRxivPreprintOct 15, 2025

Constellation illuminates rare disease genetics

Siyuan Cheng, Qing Zhang, Xinchang Zheng…·Fritz Joachim Sedlazeck

This paper evaluates Illumina Constellation sequencing for rare disease research, showing it can detect structural variants and haplotype phasing with low DNA input and existing infrastructure.

2 citations

humanwhole-genome sequencing

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