Comparative analysis of genome tiling array data reveals many novel primate-specific functional RNAs in human

por Zhang, Zhaolei, Pang, Andy Wing Chun, Gerstein, Mark
Publicado 2007

Delivery of gene targeting siRNAs to breast cancer cells using a multifunctional peptide complex that promotes both targeted delivery and endosomal release

por Bjorge, Jeffrey D., Pang, Andy, Fujita, Donald J.
Publicado en PLoS One (2017)

SIMPROT: Using an empirically determined indel distribution in simulations of protein evolution

por Pang, Andy, Smith, Andrew D, Nuin, Paulo AS, Tillier, Elisabeth RM
Publicado 2005

Positional Homology in Bacterial Genomes

por Burgetz, Ingrid J., Shariff, Salimah, Pang, Andy, Tillier, Elisabeth R. M.
Publicado 2007

Simultaneous siRNA Targeting of Src and Downstream Signaling Molecules Inhibit Tumor Formation and Metastasis of a Human Model Breast Cancer Cell Line

por Bjorge, Jeffrey D., Pang, Andy S., Funnell, Melanie, Chen, Ke Yun, Diaz, Roman, Magliocco, Anthony M., Fujita, Donald J.
Publicado 2011

Performance of High-Throughput Sequencing for the Discovery of Genetic Variation Across the Complete Size Spectrum

por Pang, Andy Wing Chun, MacDonald, Jeffrey R., Yuen, Ryan K. C., Hayes, Vanessa M., Scherer, Stephen W.
Publicado 2013

Src Regulates the Activity of the ING1 Tumor Suppressor

por Yu, Lisa, Thakur, Satbir, Leong-Quong, Rebecca YY., Suzuki, Keiko, Pang, Andy, Bjorge, Jeffrey D., Riabowol, Karl, Fujita, Donald J.
Publicado 2013

Combination of short-read, long-read, and optical mapping assemblies reveals large-scale tandem repeat arrays with population genetic implications

por Weissensteiner, Matthias H., Pang, Andy W.C., Bunikis, Ignas, Höijer, Ida, Vinnere-Petterson, Olga, Suh, Alexander, Wolf, Jochen B.W.
Publicado en Genome Res (2017)

Rapid creation of Arabidopsis doubled haploid lines for quantitative trait locus mapping

por Seymour, Danelle K., Filiault, Daniele L., Henry, Isabelle M., Monson-Miller, Jennifer, Ravi, Maruthachalam, Pang, Andy, Comai, Luca, Chan, Simon W. L., Maloof, Julin N.
Publicado 2012

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)

Towards a comprehensive structural variation map of an individual human genome

por Pang, Andy W, MacDonald, Jeffrey R, Pinto, Dalila, Wei, John, Rafiq, Muhammad A, Conrad, Donald F, Park, Hansoo, Hurles, Matthew E, Lee, Charles, Venter, J Craig, Kirkness, Ewen F, Levy, Samuel, Feuk, Lars, Scherer, Stephen W
Publicado 2010

Identification of Somatic Structural Variants in Solid Tumors by Optical Genome Mapping

por Goldrich, David Y., LaBarge, Brandon, Chartrand, Scott, Zhang, Lijun, Sadowski, Henry B., Zhang, Yang, Pham, Khoa, Way, Hannah, Lai, Chi-Yu Jill, Pang, Andy Wing Chun, Clifford, Benjamin, Hastie, Alex R., Oldakowski, Mark, Goldenberg, David, Broach, James R.
Publicado en J Pers Med (2021)

Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus

por Maggiolini, Flavia A. M., Cantsilieris, Stuart, D’Addabbo, Pietro, Manganelli, Michele, Coe, Bradley P., Dumont, Beth L., Sanders, Ashley D., Pang, Andy Wing Chun, Vollger, Mitchell R., Palumbo, Orazio, Palumbo, Pietro, Accadia, Maria, Carella, Massimo, Eichler, Evan E., Antonacci, Francesca
Publicado en PLoS Genet (2019)

Haplotype-resolved genomes provide insights into structural variation and gene content in Angus and Brahman cattle

por Low, Wai Yee, Tearle, Rick, Liu, Ruijie, Koren, Sergey, Rhie, Arang, Bickhart, Derek M., Rosen, Benjamin D., Kronenberg, Zev N., Kingan, Sarah B., Tseng, Elizabeth, Thibaud-Nissen, Françoise, Martin, Fergal J., Billis, Konstantinos, Ghurye, Jay, Hastie, Alex R., Lee, Joyce, Pang, Andy W. C., Heaton, Michael P., Phillippy, Adam M., Hiendleder, Stefan, Smith, Timothy P. L., Williams, John L.
Publicado en Nat Commun (2020)

Origins and functional impact of copy number variation in the human genome

por Conrad, Donald F., Pinto, Dalila, Redon, Richard, Feuk, Lars, Gokcumen, Omer, Zhang, Yujun, Aerts, Jan, Andrews, T. Daniel, Barnes, Chris, Campbell, Peter, Fitzgerald, Tomas, Hu, Min, Ihm, Chun Hwa, Kristiansson, Kati, MacArthur, Daniel G., MacDonald, Jeffrey R., Onyiah, Ifejinelo, Pang, Andy Wing Chun, Robson, Sam, Stirrups, Kathy, Valsesia, Armand, Walter, Klaudia, Wei, John, Tyler-Smith, Chris, Carter, Nigel P., Lee, Charles, Scherer, Stephen W., Hurles, Matthew E.
Publicado 2009

Assembly and diploid architecture of an individual human genome via single-molecule technologies

por Pendleton, Matthew, Sebra, Robert, Pang, Andy Wing Chun, Ummat, Ajay, Franzen, Oscar, Rausch, Tobias, Stütz, Adrian M, Stedman, William, Anantharaman, Thomas, Hastie, Alex, Dai, Heng, Fritz, Markus Hsi-Yang, Cao, Han, Cohain, Ariella, Deikus, Gintaras, Durrett, Russell E, Blanchard, Scott C, Altman, Roger, Chin, Chen-Shan, Guo, Yan, Paxinos, Ellen E, Korbel, Jan O, Darnell, Robert B, McCombie, W Richard, Kwok, Pui-Yan, Mason, Christopher E, Schadt, Eric E, Bashir, Ali
Publicado en Nat Methods (2015)

Genome-Wide Structural Variation Detection by Genome Mapping on Nanochannel Arrays

por Mak, Angel C. Y., Lai, Yvonne Y. Y., Lam, Ernest T., Kwok, Tsz-Piu, Leung, Alden K. Y., Poon, Annie, Mostovoy, Yulia, Hastie, Alex R., Stedman, William, Anantharaman, Thomas, Andrews, Warren, Zhou, Xiang, Pang, Andy W. C., Dai, Heng, Chu, Catherine, Lin, Chin, Wu, Jacob J. K., Li, Catherine M. L., Li, Jing-Woei, Yim, Aldrin K. Y., Chan, Saki, Sibert, Justin, Džakula, Željko, Cao, Han, Yiu, Siu-Ming, Chan, Ting-Fung, Yip, Kevin Y., Xiao, Ming, Kwok, Pui-Yan
Publicado en Genetics (2016)

The Diploid Genome Sequence of an Individual Human

por Levy, Samuel, Sutton, Granger, Ng, Pauline C, Feuk, Lars, Halpern, Aaron L, Walenz, Brian P, Axelrod, Nelson, Huang, Jiaqi, Kirkness, Ewen F, Denisov, Gennady, Lin, Yuan, MacDonald, Jeffrey R, Pang, Andy Wing Chun, Shago, Mary, Stockwell, Timothy B, Tsiamouri, Alexia, Bafna, Vineet, Bansal, Vikas, Kravitz, Saul A, Busam, Dana A, Beeson, Karen Y, McIntosh, Tina C, Remington, Karin A, Abril, Josep F, Gill, John, Borman, Jon, Rogers, Yu-Hui, Frazier, Marvin E, Scherer, Stephen W, Strausberg, Robert L, Venter, J. Craig
Publicado 2007

A high-quality bonobo genome refines the analysis of hominid evolution

por Mao, Yafei, Catacchio, Claudia R., Hillier, LaDeana W., Porubsky, David, Li, Ruiyang, Sulovari, Arvis, Fernandes, Jason D., Montinaro, Francesco, Gordon, David S., Storer, Jessica M., Haukness, Marina, Fiddes, Ian T., Murali, Shwetha Canchi, Dishuck, Philip C., Hsieh, PingHsun, Harvey, William T., Audano, Peter A., Mercuri, Ludovica, Piccolo, Ilaria, Antonacci, Francesca, Munson, Katherine M., Lewis, Alexandra P., Baker, Carl, Underwood, Jason G., Hoekzema, Kendra, Huang, Tzu-Hsueh, Sorensen, Melanie, Walker, Jerilyn A., Hoffman, Jinna, Thibaud-Nissen, Françoise, Salama, Sofie R., Pang, Andy W. C., Lee, Joyce, Hastie, Alex R., Paten, Benedict, Batzer, Mark A., Diekhans, Mark, Ventura, Mario, Eichler, Evan E.
Publicado en Nature (2021)

High-resolution comparative analysis of great ape genomes

por Kronenberg, Zev N., Fiddes, Ian T., Gordon, David, Murali, Shwetha, Cantsilieris, Stuart, Meyerson, Olivia S., Underwood, Jason G., Nelson, Bradley J., Chaisson, Mark J.P., Dougherty, Max L., Munson, Katherine M., Hastie, Alex R., Diekhans, Mark, Hormozdiari, Fereydoun, Lorusso, Nicola, Hoekzema, Kendra, Qiu, Ruolan, Clark, Karen, Raja, Archana, Welch, AnneMarie E., Sorensen, Melanie, Baker, Carl, Fulton, Robert S., Armstrong, Joel, Graves-Lindsay, Tina A., Denli, Ahmet M., Hoppe, Emma R., Hsieh, PingHsun, Hill, Christopher M., Pang, Andy Wing Chun, Lee, Joyce, Lam, Ernest T., Dutcher, Susan K., Gage, Fred H., Warren, Wesley C., Shendure, Jay, Haussler, David, Schneider, Valerie A., Cao, Han, Ventura, Mario, Wilson, Richard K., Paten, Benedict, Pollen, Alex, Eichler, Evan E.
Publicado en Science (2018)