new DNA sequence assembly program von Bonfield, J.K, Smith, K.F, Staden, R

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A genome-wide, end-sequenced 129Sv BAC library resource for targeting vector construction von Adams, David J., Quail, Michael A., Cox, Tony, van der Weyden, Louise, Gorick, Barbara D., Su, Qin, Chan, Wei-in, Davies, Rob, Bonfield, James K., Law, Frances, Humphray, Sean, Plumb, Bob, Liu, Pentao, Rogers, Jane, Bradley, Allan

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Priorities for nucleotide trace, sequence and annotation data capture at the Ensembl Trace Archive and the EMBL Nucleotide Sequence Database von Cochrane, Guy, Akhtar, Ruth, Aldebert, Philippe, Althorpe, Nicola, Baldwin, Alastair, Bates, Kirsty, Bhattacharyya, Sumit, Bonfield, James, Bower, Lawrence, Browne, Paul, Castro, Matias, Cox, Tony, Demiralp, Fehmi, Eberhardt, Ruth, Faruque, Nadeem, Hoad, Gemma, Jang, Mikyung, Kulikova, Tamara, Labarga, Alberto, Leinonen, Rasko, Leonard, Steven, Lin, Quan, Lopez, Rodrigo, Lorenc, Dariusz, McWilliam, Hamish, Mukherjee, Gaurab, Nardone, Francesco, Plaister, Sheila, Robinson, Stephen, Sobhany, Siamak, Vaughan, Robert, Wu, Dan, Zhu, Weimin, Apweiler, Rolf, Hubbard, Tim, Birney, Ewan

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Impact of hydroxychloroquine therapy on chronic urticaria: chronic autoimmune urticaria study and evaluation von Reeves, G. E. M., Boyle, M. J., Bonfield, J., Dobson, P., Loewenthal, M.

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2.2 Mb of contiguous nucleotide sequence from chromosome III of C. elegans von Wilson, R, Ainscough, R, Anderson, K, Baynes, C, Berks, M, Bonfield, J, Burton, J, Connell, M, Copsey, T, Cooper, J, Coulson, A, Craxton, M, Dear, S, Du, Z, Durbin, R, Favello, A, Fraser, A, Fulton, L, Gardner, A, Green, P, Hawkins, T, Hillier, L, Jier, M, Johnston, L, Jones, M, Kershaw, J, Kirsten, J, Laisster, N, Latreille, P, Lightning, J, Lloyd, C, Mortimore, B, O'Callaghan, M, Parsons, J, Percy, C, Rifken, L, Roopra, A, Saunders, D, Shownkeen, R, Sims, M, Smaldon, N, Smith, A, Smith, M, Sonnhammer, E, Staden, R, Sulston, J, Thierry-Mieg, J, Thomas, K, Vaudin, M, Vaughan, K, Waterston, R, Watson, A, Weinstock, L, Wilkinson-Sproat, J, Wohldman, P

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Automated detection of point mutations using fluorescent sequence trace subtraction von Bonfield, James K., Rada, Cristina, Staden, Rodger

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Comments on "Assessing and Managing Environmental Risk: Connecting Local Government Management with Emergency Management" von Bonfield, Thomas J.

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Petabyte-scale innovations at the European Nucleotide Archive von Cochrane, Guy, Akhtar, Ruth, Bonfield, James, Bower, Lawrence, Demiralp, Fehmi, Faruque, Nadeem, Gibson, Richard, Hoad, Gemma, Hubbard, Tim, Hunter, Christopher, Jang, Mikyung, Juhos, Szilveszter, Leinonen, Rasko, Leonard, Steven, Lin, Quan, Lopez, Rodrigo, Lorenc, Dariusz, McWilliam, Hamish, Mukherjee, Gaurab, Plaister, Sheila, Radhakrishnan, Rajesh, Robinson, Stephen, Sobhany, Siamak, Hoopen, Petra Ten, Vaughan, Robert, Zalunin, Vadim, Birney, Ewan

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Complex haplotypes, copy number polymorphisms and coding variation in two recently divergent mouse strains von Bradley, Allan, Adams, David J, Dermitzakis, Emmanouil T, Cox, Tony, Smith, James, Davies, Rob, Banerjee, Ruby, Bonfield, James, Mullikin, James C, Chung, Yeun Jun, Rogers, Jane

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The application of numerical estimates of base calling accuracy to DNA sequencing projects von Bonfield, James K., Staden, Rodger

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ZTR: a new format for DNA sequence trace data von Bonfield, James K., Staden, Rodger

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Experiment files and their application during large-scale sequencing projects von Bonfield, James K., Staden, Rodger

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Shotgun haplotyping: a novel method for surveying allelic sequence variation von Lindsay, Sarah J., Bonfield, James K., Hurles, Matthew E.

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SARS-CoV-2 Testing in the Community: Testing Positive Samples with the TaqMan SARS-CoV-2 Mutation Panel To Find Variants in Real Time von Ashford, F, Best, A, Dunn, SJ, Ahmed, Z, Siddiqui, H, Melville, J, Wilkinson, S, Mirza, J, Cumley, N, Stockton, J, Ferguson, J, Wheatley, L, Ratcliffe, E, Casey, A, Plant, T, Quick, J, Richter, A, Loman, N, McNally, A, Aggarwal, D, Blane, B, Brooks, E, Carabelli, AM, Churcher, CM, Galai, K, Girgis, ST, Gupta, RK, Hadjirin, NF, Leek, D, Ludden, C, McManus, GM, Palmer, S, Peacock, SJ, Smith, KS, Allara, E, Bibby, D, Bishop, C, Bosworth, A, Bradshaw, D, Chalker, V, Chand, M, Dabrera, G, Ellaby, N, Gallagher, E, Groves, N, Harrison, I, Hartman, H, Hopes, R, Hubb, J, Hutchings, S, Lackenby, A, Ledesma, J, Lee, D, Manesis, N, Manso, C, Mbisa, T, Miah, S, Muir, P, Myers, R, Osman, H, Patel, V, Pearson, C, Platt, S, Pymont, HM, Ramsay, M, Robinson, E, Schaefer, U, Thornton, A, Twohig, KA, Vipond, IB, Williams, D, Hamilton, WL, Warne, B, Aigrain, L, Alderton, A, Amato, R, Ariani, CV, Barrett, J, Bassett, AR, Beale, MA, Beaver, C, Bellis, KL, Betteridge, E, Bonfield, J, Bronner, IF, Chapman, MHS, Danesh, J, Davies, R, Dorman, MJ, Drury, E, Durham, J, Farr, BW, Foulser, L, Goncalves, S, Goodwin, S, Gourtovaia, M, Harrison, EM, Jackson, DK, James, K, Jamrozy, D

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From the DNA sequencer to a sequence assembly von Bonfield, J

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Trev: a DNA trace editor and viewer von Bonfield, James K., Beal, Kathryn F., Betts, Matthew J., Staden, Rodger

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Rupture of the Spleen von Bonfield, J P

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Duplication of the Urinary Tract von Bonfield, J P

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System and method for limiting computer usage von BONFIELD TERI J

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The VISTA Deep Extragalactic Observations (VIDEO) survey von Jarvis, Matt J., Bonfield, D. G., Bruce, V. A., Geach, J. E., McAlpine, K., McLure, R. J., González-Solares, E., Irwin, M., Lewis, J., Yoldas, A. Kupcu, Andreon, S., Cross, N. J. G., Emerson, J. P., Dalton, G., Dunlop, J. S., Hodgkin, S. T., Le, Fèvre O., Karouzos, M., Meisenheimer, K., Oliver, S., Rawlings, S., Simpson, C., Smail, I., Smith, D. J. B., Sullivan, M., Sutherland, W., White, S. V., Zwart, J. T. L.

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