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 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

PB1833: STREAMLINED WORKFLOW FOR ANALYZING AND REPORTING OPTICAL GENOME MAPPING FOR HEMATOLOGICAL MALIGNANCIES IN BIONANO VIA SOFTWARE

por Hastie, Alex, Bertolotti, Alicia, Hauenstein, Jen, Pang, Andy Wing Chun, Miller, Niel, Chaubey, Alka
Publicado 2023

Comparative Benchmarking of Optical Genome Mapping and Chromosomal Microarray Reveals High Technological Concordance in CNV Identification and Additional Structural Variant Refinem...

por Barseghyan, Hayk, Pang, Andy Wing Chun, Clifford, Benjamin, Serrano, Moises A., Chaubey, Alka, Hastie, Alex R.
Publicado 2023

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 2017

A Chromosome-Length Assembly of the Hawaiian Monk Seal (Neomonachus schauinslandi): A History of “Genetic Purging” and Genomic Stability

por Mohr, David W., Gaughran, Stephen J., Paschall, Justin, Naguib, Ahmed, Pang, Andy Wing Chun, Dudchenko, Olga, Aiden, Erez Lieberman, Church, Deanna M., Scott, Alan F.
Publicado 2022

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 2016

Optical Genome Mapping: Integrating Structural Variations for Precise Homologous Recombination Deficiency Score Calculation

por Sahajpal, Nikhil Shri, Mondal, Ashis K., Vashisht, Ashutosh, Singh, Harmanpreet, Pang, Andy Wing Chun, Saul, Daniel, Nivin, Omar, Hilton, Benjamin, DuPont, Barbara R., Kota, Vamsi, Savage, Natasha M., Hastie, Alex R., Chaubey, Alka, Kolhe, Ravindra
Publicado 2023

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 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 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 2020

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 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

Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologies

por Talsania, Keyur, Shen, Tsai-wei, Chen, Xiongfong, Jaeger, Erich, Li, Zhipan, Chen, Zhong, Chen, Wanqiu, Tran, Bao, Kusko, Rebecca, Wang, Limin, Pang, Andy Wing Chun, Yang, Zhaowei, Choudhari, Sulbha, Colgan, Michael, Fang, Li Tai, Carroll, Andrew, Shetty, Jyoti, Kriga, Yuliya, German, Oksana, Smirnova, Tatyana, Liu, Tiantain, Li, Jing, Kellman, Ben, Hong, Karl, Hastie, Alex R., Natarajan, Aparna, Moshrefi, Ali, Granat, Anastasiya, Truong, Tiffany, Bombardi, Robin, Mankinen, Veronnica, Meerzaman, Daoud, Mason, Christopher E., Collins, Jack, Stahlberg, Eric, Xiao, Chunlin, Wang, Charles, Xiao, Wenming, Zhao, Yongmei
Publicado 2022