Author

Sandra Crocker

Washington University in St. Louis

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· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Juana G. ManueliD· 2 shared Julie NeidichiD· 2 shared Tychele N. TurneriD· 2 shared 9P-ARCH· 1 shared Allan Micheil InnesiD· 1 shared Amber Neilson· 1 shared Amjad HoraniiD· 1 shared Anantha Kethireddy· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Juana G. ManuelORCID

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2 papers

Recent·Most cited

Whole-Genome Sequencing Reveals Individual and Cohort Level Insights into Chromosome 9p Syndromes

Yingxi Wang, Eleanor I. Sams, Rachel Slaugh, Sandra Crocker, Emily Cordova Hurtado, Sophia Tracy, Ying‐Chen Claire Hou, Christopher Markovic, Kostandin Valle, Victoria Tate, Khadija Belhassan, Elizabeth L. Appelbaum, Titilope M. Akinwe, Rodrigo Tzovenos Starosta, Yang Cao, , Tychele N. Turner

This study uses whole-genome sequencing to analyze 9p deletion and duplication syndromes, identifying key genes and structural variants, and introduces a machine learning model for syndrome prediction.

Genome Medicine · Oct 24, 2025Peer-reviewedGenetic & Genomic Medicine

High Coverage Highly Accurate Long-Read Sequencing of a Mouse Neuronal Cell Line Using the PacBio Revio Sequencer

Juana G. Manuel, Hillary B. Heins, Sandra Crocker, Julie Neidich, Lisa Sadzewicz, Luke J. Tallon, Tychele N. Turner

The paper tests the PacBio Revio sequencer by generating high-coverage long-read sequencing data for a mouse neuronal cell line and evaluates its performance in variant detection and genome assembly.

bioRxiv · Jun 6, 2023 · PreprintGenomics