Characterizing and measuring bias in sequence data

od Ross, Michael G, Russ, Carsten, Costello, Maura, Hollinger, Andrew, Lennon, Niall J, Hegarty, Ryan, Nusbaum, Chad, Jaffe, David B
Izdano 2013

Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparation

od Costello, Maura, Pugh, Trevor J., Fennell, Timothy J., Stewart, Chip, Lichtenstein, Lee, Meldrim, James C., Fostel, Jennifer L., Friedrich, Dennis C., Perrin, Danielle, Dionne, Danielle, Kim, Sharon, Gabriel, Stacey B., Lander, Eric S., Fisher, Sheila, Getz, Gad
Izdano 2013

Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platforms

od Costello, Maura, Fleharty, Mark, Abreu, Justin, Farjoun, Yossi, Ferriera, Steven, Holmes, Laurie, Granger, Brian, Green, Lisa, Howd, Tom, Mason, Tamara, Vicente, Gina, Dasilva, Michael, Brodeur, Wendy, DeSmet, Timothy, Dodge, Sheila, Lennon, Niall J., Gabriel, Stacey
Izdano u BMC Genomics (2018)

Coordinated reduction of genes of oxidative metabolism in humans with insulin resistance and diabetes: Potential role of PGC1 and NRF1

od Patti, Mary Elizabeth, Butte, Atul J., Crunkhorn, Sarah, Cusi, Kenneth, Berria, Rachele, Kashyap, Sangeeta, Miyazaki, Yoshinori, Kohane, Isaac, Costello, Maura, Saccone, Robert, Landaker, Edwin J., Goldfine, Allison B., Mun, Edward, DeFronzo, Ralph, Finlayson, Jean, Kahn, C. Ronald, Mandarino, Lawrence J.
Izdano 2003

High-quality draft assemblies of mammalian genomes from massively parallel sequence data

od Gnerre, Sante, MacCallum, Iain, Przybylski, Dariusz, Ribeiro, Filipe J., Burton, Joshua N., Walker, Bruce J., Sharpe, Ted, Hall, Giles, Shea, Terrance P., Sykes, Sean, Berlin, Aaron M., Aird, Daniel, Costello, Maura, Daza, Riza, Williams, Louise, Nicol, Robert, Gnirke, Andreas, Nusbaum, Chad, Lander, Eric S., Jaffe, David B.
Izdano 2011

Familial thrombocytopenia due to a complex structural variant resulting in a WAC-ANKRD26 fusion transcript

od Wahlster, Lara, Verboon, Jeffrey M., Ludwig, Leif S., Black, Susan C., Luo, Wendy, Garg, Kopal, Voit, Richard A., Collins, Ryan L., Garimella, Kiran, Costello, Maura, Chao, Katherine R., Goodrich, Julia K., DiTroia, Stephanie P., O’Donnell-Luria, Anne, Talkowski, Michael E., Michelson, Alan D., Cantor, Alan B., Sankaran, Vijay G.
Izdano u J Exp Med (2021)

Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome

od Collins, Ryan L., Brand, Harrison, Redin, Claire E., Hanscom, Carrie, Antolik, Caroline, Stone, Matthew R., Glessner, Joseph T., Mason, Tamara, Pregno, Giulia, Dorrani, Naghmeh, Mandrile, Giorgia, Giachino, Daniela, Perrin, Danielle, Walsh, Cole, Cipicchio, Michelle, Costello, Maura, Stortchevoi, Alexei, An, Joon-Yong, Currall, Benjamin B., Seabra, Catarina M., Ragavendran, Ashok, Margolin, Lauren, Martinez-Agosto, Julian A., Lucente, Diane, Levy, Brynn, Sanders, Stephan J., Wapner, Ronald J., Quintero-Rivera, Fabiola, Kloosterman, Wigard, Talkowski, Michael E.
Izdano u Genome Biol (2017)