Author

Shashi Kiran

University of VirginiaORCID 0000-0001-5591-4772Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Shashi Kiran1 paper · University of Hyderabad

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:experimental assay· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Ajay ChatrathiD· 2 shared Anindya DuttaiD· 2 shared Pankaj KumariD· 2 shared Shekhar SahaiD· 2 shared Teressa PaulseniD· 2 shared Zhangli SuiD· 2 shared Aakrosh RataniD· 1 shared Briana WilsoniD· 1 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

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2 shared papersGenomics

Ajay ChatrathORCID

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2 papers

Recent·Most cited

GenomicsScience AdvancesPeer-reviewedMay 15, 2020

ATAC-seq identifies thousands of extrachromosomal circular DNA in cancers and cell lines

Pankaj Kumar, Shashi Kiran, Shekhar Saha…·Anindya Dutta

The paper shows that ATAC-seq can detect thousands of extrachromosomal circular DNAs in cancer and cell lines without specific enrichment.

188 citationstop 1%

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Genetic & Genomic MedicineGenome MedicinePeer-reviewedFeb 17, 2020

The Pan-Cancer Landscape of Prognostic Germline Variants in 10,582 Patients

Ajay Chatrath, Róża K. Przanowska, Shashi Kiran…·Anindya Dutta

The paper identifies prognostic germline variants in 10,582 cancer patients using multivariate Cox regression, showing their association with patient outcomes beyond clinical data.

45 citations

humanwhole-exome sequencing

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