Skip to content

Author

Kateryna D. Makova

5 papers indexed here

We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.

Not the right person? Other researchers publish under this name.

Sep 2026

Protocol for Duplex Sequencing of Mitochondrial DNA in Single Human Oocytes.

Oocytes are densely packed with mitochondria, the energy-producing organelles that contain their own genome, mitochondrial DNA (mtDNA). Each cell contains multiple copies of mtDNA, with copy number varying among tissue types. Oocytes possess the highest mtDNA copy number, containing hundreds of thousands of mtDNA molec...

Teresa Kloimboeck, Thomas Ebner, Kateryna D. Makova et al. · 0 citations
Open access Mar 2026

A Complete Genome for the Common Marmoset

The common marmoset is a New World monkey (NWM) commonly used as a model organism to investigate questions in primate evolution and human disease, including Alzheimer’s and other neurodegenerative diseases, as well as neuropsychiatric disorders. Here we present the first telomere-to-telomere (T2T) reference genome for...

Prajna Hebbar, Tamara A. Potapova, Hailey Loucks et al. · 0 citations
Open access Aug 2026

The complete genome of a songbird.

This complete genome of a songbird serves as a public reference and illuminates avian genome architecture and function and suggests that birds possess a kinetochore-associated CENP system similar to that of mammals.

G. Formenti, Nivesh Jain, Jack A. Medico et al. · 2 citations
Sep 2026

HyphAeon: Attention on Evolution Across Deep Time Transforms Comparative Genomics

By bridging statistical phylogenetics with geometric representation learning, HyphAeon establishes comparative genomics as an interactive, high-throughput computational framework for evolutionary discovery.

Sergei L. Kosakovsky Pond, Steven Weaver, Danielle Callan et al. · 0 citations
Open access Jul 2026

Direct detection of alternative DNA conformations with long-read sequencing and machine learning approaches

It is demonstrated that it is possible to sequence permanganate-modified DNA directly using ONT, with minimal effects on the read length, yield, and alignment accuracy, and at high ONT sequencing depth, this approach can identify B-folded vs. single-stranded DNA regions in cells, with ssDNA frequently present across se...

Jacob P. Sieg, Huiqing Zeng, Lauren Heaverly et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.