Timofey Prodanov

Duesseldorf, NW, Germany

Last Updated: 09/26/2026

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Found 15 publications

HPRC2: A human pangenome reference with near-complete coverage of common genetic variation.

HPRC2: A human pangenome reference with near-complete coverage of common genetic variation.

Journal: bioRxiv : the preprint server for biology

Published: August 01, 2026

Complex structural variation, phylogeny, and disease associations of the mucin pangenome.

Complex structural variation, phylogeny, and disease associations of the mucin pangenome.

Journal: medRxiv : the preprint server for health sciences

Published: July 10, 2026

Aggregate variant calling using short reads enables population and disease studies for paralogous genes.

Aggregate variant calling using short reads enables population and disease studies for paralogous genes.

Journal: HGG advances

Published: January 11, 2026

Sequence-to-graph alignment based copy number calling using a network flow formulation.

Sequence-to-graph alignment based copy number calling using a network flow formulation.

Journal: bioRxiv : the preprint server for biology

Published: December 15, 2025

Author Correction: Complex genetic variation in nearly complete human genomes.

Author Correction: Complex genetic variation in nearly complete human genomes.

Journal: Nature

Published: August 26, 2025

Locityper: targeted genotyping of complex polymorphic genes.

Locityper: targeted genotyping of complex polymorphic genes.

Journal: bioRxiv : the preprint server for biology

Published: February 24, 2025

Complex genetic variation in nearly complete human genomes.

Complex genetic variation in nearly complete human genomes.

Journal: bioRxiv : the preprint server for biology

Published: October 07, 2024

Complex genetic variation in nearly complete human genomes.

Complex genetic variation in nearly complete human genomes.

Journal: Nature

Published: September 23, 2024

Locityper enables targeted genotyping of complex polymorphic genes.

Locityper enables targeted genotyping of complex polymorphic genes.

Journal: Nature genetics

Published: May 27, 2024

Long-read sequencing and structural variant characterization in 1,019 samples from the 1000 Genomes Project.

Long-read sequencing and structural variant characterization in 1,019 samples from the 1000 Genomes Project.

Journal: bioRxiv : the preprint server for biology

Published: April 25, 2024

Structural variation in 1,019 diverse humans based on long-read sequencing.

Structural variation in 1,019 diverse humans based on long-read sequencing.

Journal: Nature

Published: April 22, 2024

Structural and genetic diversity in the secreted mucins, MUC5AC and MUC5B.

Structural and genetic diversity in the secreted mucins, MUC5AC and MUC5B.

Journal: bioRxiv : the preprint server for biology

Published: April 02, 2024

Showing 1-12 of 15

Last Updated: 09/26/2026