A hybrid computational strategy to address WGS variant analysis in >5000 samples

por Huang, Zhuoyi, Rustagi, Navin, Veeraraghavan, Narayanan, Carroll, Andrew, Gibbs, Richard, Boerwinkle, Eric, Venkata, Manjunath Gorentla, Yu, Fuli
Publicado en BMC Bioinformatics (2016)

Reduced meiotic recombination in rhesus macaques and the origin of the human recombination landscape

por Xue, Cheng, Rustagi, Navin, Liu, Xiaoming, Raveendran, Muthuswamy, Harris, R. Alan, Venkata, Manjunath Gorentla, Rogers, Jeffrey, Yu, Fuli
Publicado en PLoS One (2020)

ITD assembler: an algorithm for internal tandem duplication discovery from short-read sequencing data

por Rustagi, Navin, Hampton, Oliver A, Li, Jie, Xi, Liu, Gibbs, Richard A., Plon, Sharon E., Kimmel, Marek, Wheeler, David A.
Publicado en BMC Bioinformatics (2016)

Extremely low-coverage whole genome sequencing in South Asians captures population genomics information

por Rustagi, Navin, Zhou, Anbo, Watkins, W. Scott, Gedvilaite, Erika, Wang, Shuoguo, Ramesh, Naveen, Muzny, Donna, Gibbs, Richard A., Jorde, Lynn B., Yu, Fuli, Xing, Jinchuan
Publicado en BMC Genomics (2017)

Practical Approaches for Whole-Genome Sequence Analysis of Heart- and Blood-Related Traits

por Morrison, Alanna C., Huang, Zhuoyi, Yu, Bing, Metcalf, Ginger, Liu, Xiaoming, Ballantyne, Christie, Coresh, Josef, Yu, Fuli, Muzny, Donna, Feofanova, Elena, Rustagi, Navin, Gibbs, Richard, Boerwinkle, Eric
Publicado en Am J Hum Genet (2017)

Genomic profiling of pediatric acute myeloid leukemia reveals a changing mutational landscape from disease diagnosis to relapse

por Farrar, Jason E., Schuback, Heather L., Ries, Rhonda E., Wai, Daniel, Hampton, Oliver A., Trevino, Lisa R., Alonzo, Todd A., Guidry Auvil, Jaime M., Davidsen, Tanja M., Gesuwan, Patee, Hermida, Leandro, Muzny, Donna M., Dewal, Ninad, Rustagi, Navin, Lewis, Lora R., Gamis, Alan S., Wheeler, David A., Smith, Malcolm A., Gerhard, Daniela S., Meshinchi, Soheil
Publicado en Cancer Res (2016)

CD56 expression marks human group 2 innate lymphoid cell divergence from a shared NK cell and group 3 innate lymphoid cell developmental pathway

por Chen, Luxi, Youssef, Youssef, Robinson, Cameron, Ernst, Gabrielle F., Carson, Mary Y., Young, Karen A., Scoville, Steven D., Zhang, Xiaoli, Harris, Regine, Sekhri, Palak, Mansour, Anthony G., Chan, Wing K., Nalin, Ansel P., Mao, Hsiaoyin C., Hughes, Tiffany, Mace, Emily M., Pan, Yinghong, Rustagi, Navin, Chatterjee, Sujash S., Gunaratne, Preethi H., Behbehani, Gregory K., Mundy-Bosse, Bethany L., Caligiuri, Michael A., Freud, Aharon G.
Publicado en Immunity (2018)

Whole-Exome Sequencing Reveals Uncaptured Variation and Distinct Ancestry in the Southern African Population of Botswana

por Retshabile, Gaone, Mlotshwa, Busisiwe C., Williams, Lesedi, Mwesigwa, Savannah, Mboowa, Gerald, Huang, Zhuoyi, Rustagi, Navin, Swaminathan, Shanker, Katagirya, Eric, Kyobe, Samuel, Wayengera, Misaki, Kisitu, Grace P., Kateete, David P., Wampande, Eddie M., Maplanka, Koketso, Kasvosve, Ishmael, Pettitt, Edward D., Matshaba, Mogomotsi, Nsangi, Betty, Marape, Marape, Tsimako-Johnstone, Masego, Brown, Chester W., Yu, Fuli, Kekitiinwa, Adeodata, Joloba, Moses, Mpoloka, Sununguko W., Mardon, Graeme, Anabwani, Gabriel, Hanchard, Neil A.
Publicado en Am J Hum Genet (2018)