Author

Johanna Heid

Albert Einstein College of MedicineORCID 0000-0001-7760-5217Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Organism:Drosophila· 1

Frequent Co-Authors

Alexander Y. MasloviD· 2 shared Jan VijgiD· 2 shared Moonsook LeeiD· 2 shared Shixiang SuniD· 2 shared Xiao DongiD· 2 shared Cristina MontagnaiD· 1 shared Elizabeth Pan· 1 shared Gordon Fan-HuangiD· 1 shared

Activity by Year

2024-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersGenomics

Alexander Y. MaslovORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintAug 8, 2024

Chimera-suppressing error-corrected sequencing enables quantitative detection of rare somatic structural-variant breakpoints in human cells

Elizabeth Pan, Shixiang Sun, Johanna Heid…·Alexander Y. Maslov

This paper introduces SMM-SV-seq, a method to detect rare somatic structural-variant breakpoints in bulk DNA with high precision and recall, validated using human and Drosophila DNA mixtures and clinical treatments.

3 citations

humanDrosophila

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GeneticsbioRxivPreprintApr 7, 2024

Evidence for negative selection against somatic mutations in fibroblasts with high N-ethyl-N-nitrosourea-induced mutation load

Ronald R. Cutler, Johanna Heid, Shixiang Sun…·Jan Vijg

The paper shows that human fibroblasts undergo negative selection against harmful mutations, maintaining growth despite high mutation loads.

1 citation

humanwhole-genome sequencing

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