An efficient pseudomedian filter for tiling microrrays

per Gerstein Mark B, Carriero Nicholas J, Royce Thomas E
Publicat 2007-06-01

An efficient pseudomedian filter for tiling microrrays

per Royce, Thomas E, Carriero, Nicholas J, Gerstein, Mark B
Publicat 2007

Whole-genome association studies on alcoholism comparing different phenotypes using single-nucleotide polymorphisms and microsatellites

per Chen, Liang, Liu, Nianjun, Wang, Shuang, Oh, Cheongeun, Carriero, Nicholas J, Zhao, Hongyu
Publicat 2005

X!!Tandem, an Improved Method for Running X!Tandem in Parallel on Collections of Commodity Computers

per Bjornson, Robert D., Carriero, Nicholas J., Colangelo, Christopher, Shifman, Mark, Cheung, Kei-Hoi, Miller, Perry L., Williams, Kenneth
Publicat 2007

Ultrasensitive measurement of hotspot mutations in tumor DNA in blood using error-suppressed multiplexed deep sequencing

per Narayan, Azeet, Carriero, Nicholas J., Gettinger, Scott N., Kluytenaar, Jeannie, Kozak, Kevin R., Yock, Torunn I., Muscato, Nicole E., Ugarelli, Pedro, Decker, Roy H., Patel, Abhijit A.
Publicat 2012

YPED: An Integrated Bioinformatics Suite and Database for Mass Spectrometry-based Proteomics Research

per Colangelo, Christopher M., Shifman, Mark, Cheung, Kei-Hoi, Stone, Kathryn L., Carriero, Nicholas J., Gulcicek, Erol E., Lam, TuKiet T., Wu, Terence, Bjornson, Robert D., Bruce, Can, Nairn, Angus C., Rinehart, Jesse, Miller, Perry L., Williams, Kenneth R.
Publicat a Genomics Proteomics Bioinformatics (2015)

Modeling molecular development of breast cancer in canine mammary tumors

per Graim, Kiley, Gorenshteyn, Dmitriy, Robinson, David G., Carriero, Nicholas J., Cahill, James A., Chakrabarti, Rumela, Goldschmidt, Michael H., Durham, Amy C., Funk, Julien, Storey, John D., Kristensen, Vessela N., Theesfeld, Chandra L., Sorenmo, Karin U., Troyanskaya, Olga G.
Publicat a Genome Res (2021)

Early Assessment of Lung Cancer Immunotherapy Response via Circulating Tumor DNA

per Goldberg, Sarah B., Narayan, Azeet, Kole, Adam J., Decker, Roy H., Teysir, Jimmitti, Carriero, Nicholas J., Lee, Angela, Nemati, Roxanne, Nath, Sameer K., Mane, Shrikant M., Deng, Yanhong, Sukumar, Nitin, Zelterman, Daniel, Boffa, Daniel J., Politi, Katerina, Gettinger, Scott N., Wilson, Lynn D., Herbst, Roy S., Patel, Abhijit A.
Publicat a Clin Cancer Res (2018)

Paired-End Mapping Reveals Extensive Structural Variation in the Human Genome

per Korbel, Jan O., Urban, Alexander Eckehart, Affourtit, Jason P., Godwin, Brian, Grubert, Fabian, Simons, Jan Fredrik, Kim, Philip M., Palejev, Dean, Carriero, Nicholas J., Du, Lei, Taillon, Bruce E., Chen, Zhoutao, Tanzer, Andrea, Saunders, A. C. Eugenia, Chi, Jianxiang, Yang, Fengtang, Carter, Nigel P., Hurles, Matthew E., Weissman, Sherman M., Harkins, Timothy T., Gerstein, Mark B., Egholm, Michael, Snyder, Michael
Publicat 2007

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

per 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., Meyer, Kyle A., Bilguvar, Kaya, Mane, Shrikant M., Šestan, Nenad, Lifton, Richard P., Günel, Murat, Roeder, Kathryn, Geschwind, Daniel H., Devlin, Bernie, State, Matthew W.
Publicat 2012

Keck Foundation Biotechnology Resource Laboratory, Yale University

per Stone, Kathryn L., Bjornson, Robert D., Blasko, Gregory G., Bruce, Can, Cofrancesco, Renee, Carriero, Nicholas J., Colangelo, Christopher M., Crawford, Janet K., Crawford, J. Myron, daSilva, Nancy C., Deluca, Joseph D., Elliott, James I., Elliott, Margaret M., Flory, P. John, Folta-Stogniew, Ewa J., Gulcicek, Erol, Kong, Yong, Lam, TuKiet T., Lee, Ji Y., Lin, Aiping, LoPresti, Mary B., Mane, Shrikant M., McMurray, Walter J., Tikhonova, Irina R., Westman, Sheila, Williams, Nancy A., Wu, Terence L., Hongyu, Zhao, Williams, Kenneth R.
Publicat 2008

De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder

per Dong, Shan, Walker, Michael F., Carriero, Nicholas J., DiCola, Michael, Willsey, A. Jeremy, Ye, Adam Y., Waqar, Zainulabedin, Gonzalez, Luis E., Overton, John D., Frahm, Stephanie, Keaney, John F., Teran, Nicole A., Dea, Jeanselle, Mandell, Jeffrey D., Bal, Vanessa Hus, Sullivan, Catherine A., DiLullo, Nicholas M., Khalil, Rehab O., Gockley, Jake, Yuksel, Zafer, Sertel, Sinem M., Ercan-Sencicek, A. Gulhan, Gupta, Abha R., Mane, Shrikant M., Sheldon, Michael, Brooks, Andrew I., Roeder, Kathryn, Devlin, Bernie, State, Matthew W., Wei, Liping, Sanders, Stephan J.
Publicat 2014

De novo mutations in histone modifying genes in congenital heart disease

per 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, Kaltman, Jonathan R., Kaski, Juan, Kim, Richard, Kline, Jennie K., Lee, Teresa, Leipzig, Jeremy, Lopez, Alexander, Mane, Shrikant M., Mitchell, Laura E., Newburger, Jane W., Parfenov, Michael, Pe'er, Itsik, Porter, George, Roberts, Amy, Sachidanandam, Ravi, Sanders, Stephan J., Seiden, Howard S., State, Mathew W., Subramanian, Sailakshmi, Tikhonova, Irina R., Wang, Wei, Warburton, Dorothy, White, Peter S., Williams, Ismee A., Zhao, Hongyu, Seidman, Jonathan G., Brueckner, Martina, Chung, Wendy K., Gelb, Bruce D., Goldmuntz, Elizabeth, Seidman, Christine E., Lifton, Richard P.
Publicat 2013