Julia Markowski

Harvard University

Full Professor(heuristic)

Cancer Genomics and Diagnostics · Cancer Research

h-index28

i10-index33

Publications68

Citations15,444

Grants

No NSF/NIH grants on record.

Lab Funding Health

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In-Field Influence

0.0005

PageRank within Cancer Research co-authorship network

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Admission Signals

New paper: Haplotype-resolved genome architecture mapping uncovers pervasive structural heterogeneity between human homologous chromosomes (bioRxiv (Cold Spring Harbor Laboratory))2026-06-18
New preprint: Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read data2025-10-14

Data Freshness

Publications as of 2026-07-01
Grants as of 2026-06-30

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ORCID: 0000-0002-0573-7832

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Recent Publications

Last 2 years · showing 9 of 9

Haplotype-resolved genome architecture mapping uncovers pervasive structural heterogeneity between human homologous chromosomes
bioRxiv (Cold Spring Harbor Laboratory) · 2026-06-18
Extended data for manuscript "Haplotype-resolved genome architecture mapping uncovers pervasive structural heterogeneity between human homologous chromosomes"
Zenodo (CERN European Organization for Nuclear Research) · 2026-04-24
Extended data for manuscript "Haplotype-resolved genome architecture mapping uncovers pervasive structural heterogeneity between human homologous chromosomes"
Zenodo (CERN European Organization for Nuclear Research) · 2026-04-24 · 1 citations
Extended data for manuscript "Haplotype-resolved genome architecture mapping uncovers pervasive structural heterogeneity between human homologous chromosomes"
Zenodo (CERN European Organization for Nuclear Research) · 2026-04-18
Extended data for manuscript "Haplotype-resolved genome architecture mapping uncovers pervasive structural heterogeneity between human homologous chromosomes"
Zenodo (CERN European Organization for Nuclear Research) · 2026-04-17
Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read dataPreprint
bioRxiv (Cold Spring Harbor Laboratory) · 2025-10-14 · 1 citations
The Data Distillery: A Graph Framework for Semantic Integration and Querying of Biomedical DataPreprint
bioRxiv (Cold Spring Harbor Laboratory) · 2025-08-15 · 3 citations
Extensive folding variability between homologous chromosomes in mammalian cells
Molecular Systems Biology · 2025-05-06 · 5 citations
Author Correction: Genomic basis for RNA alterations in cancer
UNC Libraries · 2025-03-13

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