Pan-cancer analysis reveals technical artifacts in TCGA germline variant calls

por Buckley, Alexandra R., Standish, Kristopher A., Bhutani, Kunal, Ideker, Trey, Lasken, Roger S., Carter, Hannah, Harismendy, Olivier, Schork, Nicholas J.
Publicado en BMC Genomics (2017)

Virmid: accurate detection of somatic mutations with sample impurity inference

por Kim, Sangwoo, Jeong, Kyowon, Bhutani, Kunal, Lee, Jeong Ho, Patel, Anand, Scott, Eric, Nam, Hojung, Lee, Hayan, Gleeson, Joseph G, Bafna, Vineet
Publicado 2013

Whole-genome mutational burden analysis of three pluripotency induction methods

por Bhutani, Kunal, Nazor, Kristopher L., Williams, Roy, Tran, Ha, Dai, Heng, Džakula, Željko, Cho, Edward H., Pang, Andy W. C., Rao, Mahendra, Cao, Han, Schork, Nicholas J., Loring, Jeanne F.
Publicado en Nat Commun (2016)

Using single nuclei for RNA-seq to capture the transcriptome of postmortem neurons

por Krishnaswami, Suguna Rani, Grindberg, Rashel V, Novotny, Mark, Venepally, Pratap, Lacar, Benjamin, Bhutani, Kunal, Linker, Sara B, Pham, Son, Erwin, Jennifer A, Miller, Jeremy A, Hodge, Rebecca, McCarthy, James K, Kelder, Martin, McCorrison, Jamison, Aevermann, Brian D, Fuertes, Francisco Diez, Scheuermann, Richard H, Lee, Jun, Lein, Ed S, Schork, Nicholas, McConnell, Michael J, Gage, Fred H, Lasken, Roger S
Publicado en Nat Protoc (2016)