Author

Arvinden VR

Institute of Genomics and Integrative BiologyORCID 0000-0002-1008-1348Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:ATAC-seq· 1 Approach:Bayesian inference· 1 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Aditya Ramdas Iyer· 1 shared Grace Tzun-Wen ShawiD· 1 shared H. KimiD· 1 shared Harie Vignesh· 1 shared Hillary B. HeinsiD· 1 shared Jeffrey K. NgiD· 1 shared Juana G. ManueliD· 1 shared Mehwish NafiziD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aditya Ramdas Iyer

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2 papers

Recent·Most cited

Multi-omics Differential Inference for Functional Interpretation (MoDIFI): A Statistical Framework to Prioritize Cell Lines for Neurodevelopmental Variants

Arvinden VR, Grace Tzun-Wen Shaw, Juana G. Manuel, Timothy L. Mosbruger, Hillary B. Heins, Jeffrey K. Ng, H. Kim, Tristan J. Hayeck, Tychele N. Turner

The paper develops MoDIFI, a Bayesian framework to prioritize cell lines and regulatory regions for testing noncoding variants associated with neurodevelopmental disorders.

bioRxiv · Jan 29, 2026 · PreprintGenomics

Scalable noninvasive amplicon-based precision sequencing (SNAPseq) for genetic diagnosis and screening of β-thalassemia and sickle cell disease using a next-generation sequencing platform

Pragya Gupta, Arvinden VR, Priya Thakur, Rahul C. Bhoyar, Vinodh Saravanakumar, Narendra Varma Gottumukkala, Sangam Giri Goswami, Mehwish Nafiz, Aditya Ramdas Iyer, Harie Vignesh, Rajat Soni, Nupur Bhargava, Padma Gunda, Suman Lata Jain, Vivek Gupta, , Sivaprakash Ramalingam

This paper introduces SNAPseq, a high-throughput NGS method for detecting β-thalassemia and sickle cell disease with 100% sensitivity and specificity using noninvasive samples.

Frontiers in Molecular Biosciences · Dec 13, 2023Peer-reviewedGenetic & Genomic Medicine