Author

Stephen Gross

Illumina (United States)ORCID 0000-0003-0711-787XUnclaimed 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:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aaron M. WengeriD· 1 shared Aaron W. AdamsoniD· 1 shared Alex R. HastieiD· 1 shared Alexander A Gooden· 1 shared Alison RojasiD· 1 shared Andrew Scott LissiD· 1 shared Anthony D. SchmittiD· 1 shared Asher BryantiD· 1 shared

Activity by Year

2019-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenomics

Aaron M. WengerORCID

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2 papers

Recent·Most cited

GenomicsScientific DataPeer-reviewedJul 16, 2025

Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair

Jennifer McDaniel, Vaidehi Patel, Nathan D. Olson…·Justin M. Zook

The paper describes a comprehensive genomic dataset from a tumor-normal pair with broad consent, generated using multiple sequencing technologies for benchmarking somatic variant detection.

14 citations

humanwhole-genome sequencing

𝕏 PostBluesky

GeneticsbioRxivPreprintOct 17, 2019

The RNA Atlas, a single nucleotide resolution map of the human transcriptome

Lucía Lorenzi, Hua‐Sheng Chiu, Francisco Avila Cobos…·Pieter Mestdagh

The paper presents a comprehensive human transcriptome atlas with single-nucleotide resolution, identifying thousands of novel RNA species and regulatory interactions.

10 citations

humanbulk RNA-seq

𝕏 PostBluesky