Author

Jessica Albert

Broad Institute

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 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:variant calling· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Approach:experimental assay· 1 Organism:human· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Changrui XiaoiD· 2 shared Ivan De DiosiD· 2 shared Miguel AlmalveziD· 2 shared Seth BergeriD· 2 shared Amy Ginsburg· 1 shared Andrea J. CoheniD· 1 shared Arthur Garcia· 1 shared Arthur KoiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Changrui XiaoORCID

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2 papers

Recent·Most cited

Yield of Long-Read Genome Sequencing for Rare Disease Diagnosis in Short-Read Genome Negative Cases

Georgia Pitsava, Krista K. Bluske, Rebekah Barrick, Ivan De Dios, Cathy Duong, Kirsten Blanco, Sami Belhadj, Nida Karra, Sarah L. Stenton, Arthur Garcia, Erica Smith, Miguel Almalvez, Arthur Ko, John Harting, Stuti Joshi, , Eric J. N. Vilain

This study evaluates the diagnostic yield of long-read genome sequencing in cases where short-read sequencing failed, finding an incremental yield of 4.7% due to LR-GS's ability to detect structural variants and other complex genomic features.

medRxiv · Sep 10, 2026 · PreprintGenetic & Genomic Medicine

Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

Jessica X. Chong, Seth Berger, Samantha M. Baxter, Erica D. Smith, Changrui Xiao, Daniel G. Calame, Megan H. Hawley, E. Andres Rivera-Munoz, Stephanie P. DiTroia, Siwaar Abouhala, Jessica Albert, Miguel Almalvez, Raquel Alvarez, Mutaz Amin, Peter Anderson, , Tanner D. Jensen

The paper develops criteria for identifying, sharing, and reporting novel candidate genes in clinical genomic testing to improve diagnostic yield for Mendelian conditions.

Genetics in Medicine · Jun 26, 2024Peer-reviewedGenetics