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A spatial simulation approach to account for protein structure when identifying non-random somatic mutations.
Published in:
BMC Bioinformatics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2105-15-231
By:
- Ryslik, Gregory A.;
- Yuwei Cheng;
- Kei-Hoi Cheung;
- Bjornson, Robert D.;
- Zelterman, Daniel;
- Modis, Yorgo;
- Hongyu Zhao
Publication type:
Article
Integrating Sequencing Technologies in Personal Genomics: Optimal Low Cost Reconstruction of Structural Variants.
Published in:
PLoS Computational Biology, 2009, v. 5, n. 7, p. 1, doi. 10.1371/journal.pcbi.1000432
By:
- Jiang Du;
- Bjornson, Robert D.;
- Zhang, Zhengdong D.;
- Yong Kong;
- Snyder, Michael;
- Gerstein, Mark B.
Publication type:
Article
De novo mutations in histone-modifying genes in congenital heart disease.
Published in:
Nature, 2013, v. 498, n. 7453, p. 220, doi. 10.1038/nature12141
By:
- Zaidi, Samir;
- Choi, Murim;
- Wakimoto, Hiroko;
- Ma, Lijiang;
- Jiang, Jianming;
- Overton, John D.;
- Romano-Adesman, Angela;
- Bjornson, Robert D.;
- Breitbart, Roger E.;
- Brown, Kerry K.;
- Carriero, Nicholas J.;
- Cheung, Yee Him;
- Deanfield, John;
- DePalma, Steve;
- Fakhro, Khalid A.;
- Glessner, Joseph;
- Hakonarson, Hakon;
- Italia, Michael J.;
- Kaltman, Jonathan R.;
- Kaski, Juan
Publication type:
Article
De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Published in:
Nature, 2012, v. 485, n. 7397, p. 237, doi. 10.1038/nature10945
By:
- Sanders, Stephan J.;
- Murtha, Michael T.;
- Gupta, Abha R.;
- Murdoch, John D.;
- Raubeson, Melanie J.;
- Willsey, A. Jeremy;
- Ercan-Sencicek, A. Gulhan;
- DiLullo, Nicholas M.;
- Parikshak, Neelroop N.;
- Stein, Jason L.;
- Walker, Michael F.;
- Ober, Gordon T.;
- Teran, Nicole A.;
- Song, Youeun;
- El-Fishawy, Paul;
- Murtha, Ryan C.;
- Choi, Murim;
- Overton, John D.;
- Bjornson, Robert D.;
- Carriero, Nicholas J.
Publication type:
Article

Found: 4

A spatial simulation approach to account for protein structure when identifying non-random somatic mutations.

Integrating Sequencing Technologies in Personal Genomics: Optimal Low Cost Reconstruction of Structural Variants.

De novo mutations in histone-modifying genes in congenital heart disease.

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.