Identifying novel constrained elements by exploiting biased substitution patterns by Guttman, Mitchell, Garber, Manuel, Clamp, Michele, Zody, Michael C., Friedman, Nir, Xie, Xiaohui

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Closing gaps in the human genome using sequencing by synthesis by Arachchi, Harindra M., Green, Lisa M., Zody, Michael C., Lennon, Niall, Gnerre, Sante, Berlin, Aaron M., Nusbaum, Chad, Garber, Manuel

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<it>De novo</it> assembly of highly diverse viral populations by Yang Xiao, Charlebois Patrick, Gnerre Sante, Coole Matthew G, Lennon Niall J, Levin Joshua Z, Qu James, Ryan Elizabeth M, Zody Michael C, Henn Matthew R

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Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing by Kirby, Andrew, Gnirke, Andreas, Jaffe, David B., Baresova, Veronika, Pochet, Nathalie, Blumenstiel, Brendan, Ye, Chun, Aird, Daniel, Stevens, Christine, Robinson, James T., Cabili, Moran N., Gat-Viks, Irit, Kelliher, Edward, Daza, Riza, DeFelice, Matthew, Hulkova, Helena, Sovova, Jana, Vylet'al, Petr, Antignac, Corinne, Guttman, Mitchell, Handsaker, Robert E., Perrin, Danielle, Steelman, Scott, Sigurdsson, Snaevar, Scheinman, Steven J., Sougnez, Carrie, Cibulskis, Kristian, Parkin, Melissa, Green, Todd, Rossin, Elizabeth, Zody, Michael C., Xavier, Ramnik J., Pollak, Martin R., Alper, Seth L., Lindblad-Toh, Kerstin, Gabriel, Stacey B., Hart, P. Suzanne, Regev, Aviv, Nusbaum, Chad, Kmoch, Stanislav, Bleyer, Anthony J., Daly, Mark J., Lander, Eric Steven

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