Author

Tejasvi S. Niranjan

Johns Hopkins UniversityORCID 0000-0002-6458-2017Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:whole-genome sequencing· 2 Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:Hi-C· 1

Frequent Co-Authors

Alexander V. FavoroviD· 1 shared Amelie T. van der VeniD· 1 shared An‐Sofie SchoonjansiD· 1 shared Andrea Rueegger· 1 shared Andrey A. MironoviD· 1 shared Anna Esteve‐CodinaiD· 1 shared Anna JanseniD· 1 shared Anne Schulz· 1 shared

Activity by Year

2017-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperBioinformatics

Alexander V. FavorovORCID

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2 papers

Recent·Most cited

Long-read genome sequencing resolves complex structural variants in exome-negative developmental and epileptic encephalopathy

Joohyun Park, Zakaria Eddafir, Josua Kegele, Davide Mei, Noor Smal, Christina Vossler-Wolf, Kornelia Ellwanger, Charissa Millevert, Merel Swinnen, Robert J. Lauerer, Heidi Loeffler, Thomas Ott, German M. Demidov, Michael Alber, Francesca Bisulli, , Holger Lerche

This study evaluates the diagnostic value of long-read genome sequencing in DEE patients, finding it particularly effective for resolving complex structural variants not detected by short-read sequencing.

medRxiv · Oct 28, 2026 · PreprintGenetic & Genomic Medicine

StereoGene: Rapid Estimation of Genomewide Correlation of Continuous or Interval Feature Data

Elena D. Stavrovskaya, Tejasvi S. Niranjan, Elana Judith Fertig, Sarah J. Wheelan, Alexander V. Favorov, Andrey A. Mironov

StereoGene estimates genomewide correlation of continuous genomic features, revealing spatial relationships between epigenomic features and splicing sites.

Bioinformatics · Jun 12, 2017Peer-reviewedBioinformatics