Author

John C. Herriges

Children's Mercy HospitalORCID 0000-0002-4478-6450Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:long-read sequencing· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Chengpeng Bi· 2 shared Elena A. RepnikovaiD· 2 shared Tomi PastineniD· 2 shared Adam F. JohnsoniD· 1 shared Adam Walter· 1 shared Alan S. GamisiD· 1 shared Asher BryantiD· 1 shared Ayşe Gökçe KeşküşiD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Chengpeng Bi

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 15, 2025

Expanded map of genomic imprinting reveals insight into human disease

Craig Smail, Warren Cheung, Boryana S. Koseva…·Elin Grundberg

The paper expands the human genomic imprinting map using long-read sequencing and GWAS integration, revealing new disease-associated loci and maternal/paternal imprinting patterns.

1 citation

humanwhole-genome sequencing

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Genetic & Genomic MedicinemedRxivPreprintNov 5, 2024

Successful classification of clinical pediatric leukemia genetic subtypes via structural variant detection using HiFi long-read sequencing

Lisa A. Lansdon, Byunggil Yoo, Ayşe Gökçe Keşküş…·Midhat S. Farooqi

This study shows that HiFi long-read sequencing can detect clinically relevant structural variants in pediatric leukemia, improving subtype classification.

5 citations

humanlong-read sequencing

𝕏 PostBluesky