Author

Zena Ng

Stanford Health CareORCID 0000-0001-9789-4212Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:benchmark study· 1 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Alexander M MilleriD· 1 shared Anne O’Donnell‐LuriaiD· 1 shared Dena R. MataloniD· 1 shared Devon E. BonneriD· 1 shared Euan Angus AshleyiD· 1 shared Evin M. PadhiiD· 1 shared Gabrielle LemireiD· 1 shared Güney BademciiD· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexander M MillerORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineThe American Journal of Human GeneticsPeer-reviewedSep 19, 2025

Transcriptome-wide outlier approach identifies individuals with minor spliceopathies

Taylor M. Maurer, Rodrigo Mendez, Rachel A. Ungar…·Vijay S Ganesh

The paper identifies individuals with minor spliceopathies by analyzing transcriptome-wide splicing outliers in RNA-seq data from rare disease cohorts.

19 citationstop 3%

humanbulk RNA-seq

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BioinformaticsBMC BioinformaticsPeer-reviewedFeb 24, 2021

Benchmarking workflows to assess performance and suitability of germline variant calling pipelines in clinical diagnostic assays.

Vandhana Krishnan, Sowmi Utiramerur, Zena Ng…·Euan Angus Ashley

The paper benchmarks germline variant calling pipelines in clinical assays using cloud-based workflows and GIAB reference samples to evaluate performance across genomic regions and variant types.

15 citations

humanwhole-exome sequencing

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