Author

Xiaojun Feng

NewYork–Presbyterian HospitalORCID 0000-0003-3490-2873Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Adrian Y. TaniD· 1 shared Alessandro RomaneliD· 1 shared Andrea SboneriD· 1 shared Colin C. PritchardiD· 1 shared Francesca DemichelisiD· 1 shared Hanna RennertiD· 1 shared Himisha BeltraniD· 1 shared Ivan H. IossifoviD· 1 shared

Activity by Year

2017-2017 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Adrian Y. TanORCID

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1 paper

Recent·Most cited

GenomicsbioRxivPreprintMar 1, 2017

Discovery and reporting of clinically-relevant germline variants in advanced cancer patients assessed using whole-exome sequencing

Tuo Zhang, Alessandro Romanel, Kenneth Eng…·Olivier Elemento

This study reports that 17% of advanced cancer patients have clinically relevant germline variants, with higher rates of cancer-associated variants compared to control cohorts.

2 citations

humanwhole-exome sequencing

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