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Whole-genome sequencing of patients with rare diseases in a national health system.

E. Turro, W. Astle, K. Megy, S. Gräf, D. Greene, O. Shamardina, H. Allen, A. Sanchis-Juan, M. Frontini, C. Thys, J. Stephens, R. Mapeta, O. Burren, K. Downes, M. Haimel, S. Tuna, S. Deevi, T. Aitman, D. Bennett, P. Calleja, K. Carss, M. Caulfield, P. Chinnery, P. Dixon, D. Gale, R. James, A. Koziell, M. Laffan, A. Levine, E. Maher, H. Markus, J. Morales, N. Morrell, A. Mumford, E. Ormondroyd, S. Rankin, A. Rendon, S. Richardson, I. Roberts, N. Roy, M. Saleem, K. Smith, H. Stark, R. Tan, A. Themistocleous, A. Thrasher, H. Watkins, A. Webster, M. Wilkins, C. Williamson, J. Whitworth, S. Humphray, D. Bentley, S. Abbs, L. Abulhoul, J. Adlard, M. Ahmed, H. Alachkar, D. Allsup, J. Almeida-King, P. Ancliff, R. Antrobus, R. Armstrong, G. Arno, S. Ashford, A. Attwood, P. Aurora, C. Babbs, C. Bacchelli, T. Bakchoul, S. Banka, T. Bariana, J. Barwell, J. Batista, H. Baxendale, P. Beales, A. Bierzynska, T. Biss, M. Bitner-Glindzicz, G. Black, M. Bleda, I. Blesneac, D. Bockenhauer, H. Bogaard, C. Bourne, S. Boyce, J. Bradley, E. Bragin, G. Breen, P. Brennan, C. Brewer, M. Brown, A. Browning, M. Browning, R. Buchan, M. Buckland, T. Bueser, C. Diz, J. Burn, S. Burns, N. Burrows, C. Campbell, G. Carr-White, R. Casey, J. Chambers, J. Chambers, M. Chan, C. Cheah, F. Cheng, M. Chitre, M. Christian, C. Church, J. Clayton-Smith, M. Cleary, N. Brod, G. Coghlan, E. Colby, T. Cole, J. Collins, P. Collins, C. Colombo, C. Compton, R. Condliffe, S. Cook, H. Cook, N. Cooper, P. Corris, A. Furnell, F. Cunningham, N. Curry, A. Cutler, M. Daniels, M. Dattani, L. Daugherty, J. Davis, A. Soyza, T. Dent, C. Deshpande, E. Dewhurst, S. Douzgou, A. Drazyk, E. Drewe, D. Duarte, T. Dutt, J. Edgar, K. Edwards, W. Egner, M. Ekani, P. Elliott, W. Erber, M. Erwood, M. Estiu, D. Evans, G. Evans, T. Everington, M. Eyries, H. Fassihi, R. Favier, J. Findhammer, D. Fletcher, F. Flinter, R. Floto, T. Fowler, J. Fox, A. Frary, C. French, K. Freson, H. Gall, V. Ganesan, M. Gattens, C. Geoghegan, T. Gerighty, A. Gharavi, S. Ghio, H. Ghofrani, J. Gibbs, K. Gibson, K. Gilmour, B. Girerd, N. Gleadall, S. Goddard, D. Goldstein, K. Gomez, P. Gordins, D. Gosal, J. Graham, L. Grassi, L. Greenhalgh, A. Greinacher, P. Gresele, P. Griffiths, S. Grigoriadou, R. Grocock, D. Grozeva, M. Gurnell, S. Hackett, C. Hadinnapola, W. Hague, R. Hague, M. Hall, H. Hanson, E. Haque, K. Harkness, A. Harper, C. Harris, D. Hart, A. Hassan, G. Hayman, A. Henderson, A. Herwadkar, J. Hoffman, S. Holden, R. Horvath, H. Houlden, A. Houweling, L. Howard, F. Hu, G. Hudson, J. Hughes, A. Huissoon, M. Humbert, S. Hunter, M. Hurles, M. Irving, L. Izatt, S. Johnson, S. Jolles, J. Jolley, D. Josifova, N. Jurkute, T. Karten, J. Karten, M. Kasanicki, H. Kazkaz, R. Kazmi, P. Kelleher, A. Kelly, W. Kelsall, C. Kempster, D. Kiely, N. Kingston, R. Klima, N. Koelling, M. Kostadima, G. Kovacs, R. Kreuzhuber, T. Kuijpers, A. Kumar, D. Kumararatne, M. Kurian, F. Lalloo, M. Lambert, A. Lawrie, D. Layton, N. Lench, C. Lentaigne, T. Lester, R. Linger, H. Longhurst, L. Lorenzo, E. Louka, P. Lyons, R. Machado, R. Ross, B. Madan, J. Maimaris, S. Malka, S. Mangles, K. Marchbank, S. Marks, H. Marschall, A. Marshall, J. Martin, M. Mathias, E. Matthews, H. Maxwell, P. McAlinden, M. McCarthy, H. McKinney, A. McMahon, S. Meacham, A. Mead, I. Castello, S. Mehta, M. Michaelides, C. Millar, S. Mohammed, S. Moledina, D. Montani, A. Moore, M. Mozere, K. Muir, A. Nemeth, W. Newman, M. Newnham, S. Noorani, P. Nurden, J. O'Sullivan, S. Obaji, C. Odhams, S. Okoli, A. Olschewski, H. Olschewski, K. Ong, S. Oram, W. Ouwehand, C. Palles, S. Papadia, S. Park, D. Parry, S. Patel, J. Paterson, A. Peacock, S. Pearce, J. Peden, K. Peerlinck, C. Penkett, J. Pepke-Zaba, R. Petersen, C. Pilkington, K. Poole, R. Prathalingam, B. Psaila, A. Pyle, R. Quinton, S. Rahman, A. Rao, F. Raymond, P. Rayner-Matthews, C. Rees, T. Renton, C. Rhodes, A. Rice, A. Richter, L. Robert, A. Rogers, S. Rose, R. Ross-Russell, C. Roughley, D. Ruddy, O. Sadeghi-Alavijeh, N. Samani, C. Samarghitean, R. Sargur, R. Sarkany, S. Satchell, S. Savic, J. Sayer, G. Sayer, L. Scelsi, A. Schaefer, S. Schulman, R. Scott, M. Scully, C. Searle, W. Seeger, A. Sen, W. Sewell, D. Seyres, N. Shah, S. Shapiro, A. Shaw, P. Short, K. Sibson, L. Side, I. Simeoni, M. Simpson, M. Sims, S. Sivapalaratnam, D. Smedley, K. Smith, K. Snape, N. Soranzo, F. Soubrier, L. Southgate, O. Spasic-Boskovic, S. Staines, E. Staples, C. Steward, K. Stirrups, A. Stuckey, J. Suntharalingam, E. Swietlik, P. Syrris, R. Tait, K. Talks, K. Tate, J. Taylor, J. Taylor, J. Thaventhiran, E. Thomas, D. Thomas, M. Thomas, P. Thomas, K. Thomson, G. Threadgold, T. Tilly, M. Tischkowitz, C. Titterton, J. Todd, C. Toh, B. Tolhuis, I. Tomlinson, M. Toshner, M. Traylor, C. Treacy, P. Treadaway, R. Trembath, W. Turek, P. Twiss, T. Vale, C. Geet, N. van Zuydam, M. Vandekuilen, A. Vandersteen, M. Vazquez-Lopez, J. von Ziegenweidt, A. Vonk-Noordegraaf, A. Wagner, Q. Waisfisz, S. Walker, N. Walker, K. Walter, J. Ware, C. Watt, L. Wedderburn, W. Wei, S. Welch, J. Wessels, S. Westbury, J. Westwood, J. Wharton, D. Whitehorn, A. Wilkie, B. Wilson, E. Wong, N. Wood, Y. Wood, C. Woods, E. Woodward, S. Wort, A. Worth, M. Wright, K. Yates, P. Yong, T. Young, P. Yu, P. Yu-Wai-Man, and E. Zlamalova. Nat., 583 (7814): 96-102 (2020)

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Stefan Andreas Gräf

Stefan Graf

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Ensembl 2006.E. Birney, T. Andrews, M. Cáccamo, Y. Chen, L. Clarke, G. Coates, T. Cox, F. Cunningham, V. Curwen, T. Cutts and 41 other author(s). Nucleic Acids Res., 34 (Database-Issue): 556-561 (2006)Optimising oligonucleotide array design for ChIP-on-chip.F. Nielsen, S. Gräf, X. Zhang, S. Kurtz, S. Denissov, R. Green, E. Birney, P. Flicek, M. Huynen, and H. Stunnenberg. BMC Bioinform., (2007)HGVA: the Human Genome Variation Archive.J. López, J. Coll, M. Haimel, S. Kandasamy, J. Tárraga, P. Furió-Tarí, W. Bari, M. Bleda, A. Rueda, S. Gräf and 3 other author(s). Nucleic Acids Res., 45 (Webserver-Issue): W189-W194 (2017)The Distributed Annotation System for integration of biological dataA. Prlic, E. Birney, T. Cox, T. Down, R. Finn, S. Gräf, D. Jackson, A. Kahari, E. Kulesha, R. Pettett and 3 other author(s). Proc. of the 3rd International Workshop on Data Integration in the Life Sciences (DILS), (2006)Whole-genome sequencing of patients with rare diseases in a national health system.E. Turro, W. Astle, K. Megy, S. Gräf, D. Greene, O. Shamardina, H. Allen, A. Sanchis-Juan, M. Frontini, C. Thys and 439 other author(s). Nat., 583 (7814): 96-102 (2020)The Distributed Annotation System for Integration of Biological Data.A. Prlic, E. Birney, T. Cox, T. Down, R. Finn, S. Gräf, D. Jackson, A. Kähäri, E. Kulesha, R. Pettett and 3 other author(s). DILS, volume 4075 of Lecture Notes in Computer Science, page 195-203. Springer, (2006)Optimized design and assessment of whole genome tiling arrays.S. Gräf, F. Nielsen, S. Kurtz, M. Huynen, E. Birney, H. Stunnenberg, and P. Flicek. ISMB/ECCB (Supplement of Bioinformatics), page 195-204. (2007)H-MMI - Interaktionskonzept für variable Daten und Funktionen.S. Graf, A. Keinath, V. Broy, and G. Rigoll. MuC (Workshopband), page 31-36. Verlag der Bauhaus-Universität Weimar, (2007)Flexibilisierung der Arbeit{. Graf, {. Henneberger, and {. Schmid. Haupt, Bern u.a., (2000)In-car interaction using search-based user interfaces.S. Graf, W. Spiessl, A. Schmidt, A. Winter, and G. Rigoll. CHI, page 1685-1688. ACM, (2008)

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Disambiguation of "Gräf, Stefan"

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Whole-genome sequencing of patients with rare diseases in a national health system.

Please choose a person to relate this publication to

Stefan Andreas Gräf

Stefan Graf

Stefan Graf

Stefan Graf

Stefan Graf

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Gräf, Stefan"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Whole-genome sequencing of patients with rare diseases in a national health system.

Please choose a person to relate this publication to

Stefan Andreas Gräf

Stefan Graf

Stefan Graf

Stefan Graf

Stefan Graf

Other publications of authors with the same name

Disambiguation

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Whole-genome sequencing of patients with rare diseases in a national health system.