Author

Ivana Pačar

University of California, Santa CruzORCID 0009-0008-4626-7831Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:genome assembly· 1 Assay:long-read sequencing· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Mark DiekhansiD· 2 shared Prajna HebbariD· 2 shared Sofie R. SalamaiD· 2 shared Adriana Estela Sedeño-CortésiD· 1 shared Alessandro RosaiD· 1 shared Alexander G. IoannidisiD· 1 shared Allison N. RozanskiiD· 1 shared Andrea Tanzer AiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenomics

Mark DiekhansORCID

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2 papers

Recent·Most cited

GenomicsCell GenomicsPeer-reviewedMar 30, 2026

Genetic diversity and regulatory features of human-specific NOTCH2NL duplications

Taylor D. Real, Prajna Hebbar, DongAhn Yoo…·Evan E. Eichler

The paper characterizes the genetic diversity and regulatory features of human-specific NOTCH2NL duplications using long-read sequencing and organoid models.

5 citationstop 1%

humanlong-read sequencing

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GenomicsbioRxivPreprintMar 30, 2026

The diploid reference genome of a human embryonic stem cell line

Ivana Pačar, Matteo Tommaso Ungaro, Ying Chen…·Simona Giunta

The paper presents the first telomere-to-telomere diploid reference genome of the human embryonic stem cell line H9, revealing genomic features and ancestry.

1 citation

humanwhole-genome sequencing

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