-
1
-
-
10244273850
-
Experiences with eScience workflow specification and enactment in bioinformatics
-
Addis, M., Ferris, J., Greenwood, M., Li, P., Marvin, D., Oinn, T. and Wipat, A. (2003) Experiences with eScience workflow specification and enactment in bioinformatics. In Proceedings of the UK e-Science All Hands Meeting 2003, pp. 459-466.
-
(2003)
Proceedings of the UK E-Science All Hands Meeting 2003
, pp. 459-466
-
-
Addis, M.1
Ferris, J.2
Greenwood, M.3
Li, P.4
Marvin, D.5
Oinn, T.6
Wipat, A.7
-
2
-
-
0030801002
-
Gapped BLAST and PSI-BLAST: A new generation of protein database search programs
-
Altschul, S.F., Thomas, L., Madden, A., Schaffer, A., Zhang J., Zhang, Z., Miller, W. and Lipman, D.J. (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res., 25, 3389-3402.
-
(1997)
Nucleic Acids Res.
, vol.25
, pp. 3389-3402
-
-
Altschul, S.F.1
Thomas, L.2
Madden, A.3
Schaffer, A.4
Zhang, J.5
Zhang, Z.6
Miller, W.7
Lipman, D.J.8
-
3
-
-
6044224544
-
Globally distributed object identification for biological knowledgebases
-
Clark, T., Martin, S. and Liefeld, T. (2004) Globally distributed object identification for biological knowledgebases. Brief. Bioinform., 5, 59-70.
-
(2004)
Brief. Bioinform.
, vol.5
, pp. 59-70
-
-
Clark, T.1
Martin, S.2
Liefeld, T.3
-
4
-
-
0033036631
-
Comparative mapping of the region of human chromosome 7 deleted in Williams syndrome
-
DeSilva, U., Massa, H., Trask, B. and Green, E. (1999) Comparative mapping of the region of human chromosome 7 deleted in Williams syndrome. Genome Res., 9, 428-436.
-
(1999)
Genome Res.
, vol.9
, pp. 428-436
-
-
DeSilva, U.1
Massa, H.2
Trask, B.3
Green, E.4
-
5
-
-
0027185655
-
Hemizygosity at the elastin locus in a development disorder, Williams syndrome
-
Ewart, A., Morris, C., Atkinson, D., Jin, W., Sternes, K., Spallone, P., Stock, A., Leppert, M. and Keating, M. (1993) Hemizygosity at the elastin locus in a development disorder, Williams syndrome. Nat. Genet., 5, 11-16.
-
(1993)
Nat. Genet.
, vol.5
, pp. 11-16
-
-
Ewart, A.1
Morris, C.2
Atkinson, D.3
Jin, W.4
Sternes, K.5
Spallone, P.6
Stock, A.7
Leppert, M.8
Keating, M.9
-
6
-
-
0003982659
-
-
Morgan Kaufmann Publishers, San Mateo, CA
-
Foster, I., and Kesselman, C. (eds) (2003) Blueprint for a New Computing Infrastructure, 2nd edn. Morgan Kaufmann Publishers, San Mateo, CA.
-
(2003)
Blueprint for a New Computing Infrastructure, 2nd Edn.
-
-
Foster, I.1
Kesselman, C.2
-
7
-
-
0003918059
-
The physiology of the Grid: An open Grid services architecture for distributed systems integration
-
Foster, I., Kesselman, C., Nick, J. and Tuecke, S. (2002) The physiology of the Grid: an open Grid services architecture for distributed systems integration. Technical report of the Global Grid Forum.
-
(2002)
Technical Report of the Global Grid Forum
-
-
Foster, I.1
Kesselman, C.2
Nick, J.3
Tuecke, S.4
-
8
-
-
26444525909
-
The myGrid project: Services, architecture and demonstrator
-
University of Manchester, Manchester, UK
-
Goble, C., Wroe, C., Stevens, R. and myGrid consortium (2003) The myGrid project: services, architecture and demonstrator. In Proceedings of the UK e-Science programme All Hands Meeting, University of Manchester, Manchester, UK.
-
(2003)
Proceedings of the UK E-Science Programme All Hands Meeting
-
-
Goble, C.1
Wroe, C.2
Stevens, R.3
-
9
-
-
0037462510
-
Science and the semantic web
-
Hendler, J. (2003) Science and the semantic web. Science, 299, 520-521.
-
(2003)
Science
, vol.299
, pp. 520-521
-
-
Hendler, J.1
-
10
-
-
0038495746
-
The DNA Sequence of human chromosome 7
-
Hillier, L.W., Fulton, R.S., Fulton, L.A., Graves, T.A., Pepkin, K.H., Wagner-McPherson, C., Layman, D., Maas, J., Jaeger, S., Walker, R. et al. (2003) The DNA Sequence of human chromosome 7. Nature, 242, 157-164.
-
(2003)
Nature
, vol.242
, pp. 157-164
-
-
Hillier, L.W.1
Fulton, R.S.2
Fulton, L.A.3
Graves, T.A.4
Pepkin, K.H.5
Wagner-McPherson, C.6
Layman, D.7
Maas, J.8
Jaeger, S.9
Walker, R.10
-
11
-
-
0034284437
-
Repbase update: A database and an electronic journal of repetitive elements
-
Jurka J. (2000) Repbase update: a database and an electronic journal of repetitive elements. Trend Genet., 9, 418-420.
-
(2000)
Trend Genet.
, vol.9
, pp. 418-420
-
-
Jurka, J.1
-
12
-
-
3543137973
-
Resource description framework (RDF): Concepts and abstract syntax
-
Klyne, G. and Carroll, J.J. (2003) Resource description framework (RDF): Concepts and abstract syntax. W3C Proposed Recommendation.
-
(2003)
W3C Proposed Recommendation
-
-
Klyne, G.1
Carroll, J.J.2
-
14
-
-
0023688145
-
The natural history of Williams syndrome: Physical characteristics
-
Morris, C. (1988) The natural history of Williams syndrome: physical characteristics. J. Paediatr., 113, 318-326.
-
(1988)
J. Paediatr.
, vol.113
, pp. 318-326
-
-
Morris, C.1
-
15
-
-
0032775557
-
Williams-Beuren syndrome: Unraveling the mysteries of a microdeletion disorder
-
Osborne, L. (1999) Williams-Beuren syndrome: unraveling the mysteries of a microdeletion disorder. Mol. Genet. Metab., 67, 1-10.
-
(1999)
Mol. Genet. Metab.
, vol.67
, pp. 1-10
-
-
Osborne, L.1
-
16
-
-
0035179436
-
A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome
-
Osborne, L., Li, M., Pober, B., Chitayat, D., Bodurtha, J., Mandell, A., Costa, T., Grebe, T., Cox, S., Tsui, L.-C. and Scherer, S. (2001) A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome. Nat. Genet., 29, 321-325.
-
(2001)
Nat. Genet.
, vol.29
, pp. 321-325
-
-
Osborne, L.1
Li, M.2
Pober, B.3
Chitayat, D.4
Bodurtha, J.5
Mandell, A.6
Costa, T.7
Grebe, T.8
Cox, S.9
Tsui, L.-C.10
Scherer, S.11
-
17
-
-
0033939577
-
A physical map, including BAC/PAC clone contig, of the Williams-Beuren Syndrome-deletion region at 7q11.23
-
Peoples, R., Franke, Y., Wang, Y.-K., Pérez Jurado, L., Paperna, T., Cisco, M. and Francke, U. (2000) A physical map, including BAC/PAC clone contig, of the Williams-Beuren Syndrome-deletion region at 7q11.23. Am. J. Human Genet., 66, 47-68.
-
(2000)
Am. J. Human Genet.
, vol.66
, pp. 47-68
-
-
Peoples, R.1
Franke, Y.2
Wang, Y.-K.3
Pérez Jurado, L.4
Paperna, T.5
Cisco, M.6
Francke, U.7
-
18
-
-
0021259418
-
The Williams syndrome: Objective definition and diagnosis
-
Preus, M. (1984) The Williams syndrome: objective definition and diagnosis. Clin. Genet., 25, 422-428.
-
(1984)
Clin. Genet.
, vol.25
, pp. 422-428
-
-
Preus, M.1
-
19
-
-
0242339600
-
Haystack: A platform for authoring end user semantic web applications
-
Fensel, D., Sycara, K. and Mylopoulos, J. (eds), Lecture Notes in Computer Science 2870, Springer
-
Quan, D., Huynh, D. and Karger, D.R. (2003) Haystack: a platform for authoring end user semantic web applications. In Fensel, D., Sycara, K. and Mylopoulos, J. (eds), Proceedings of the 2003 international semantic web conference (ISWC 2003), Lecture Notes in Computer Science 2870, Springer, pp. 738-753.
-
(2003)
Proceedings of the 2003 International Semantic Web Conference (ISWC 2003)
, pp. 738-753
-
-
Quan, D.1
Huynh, D.2
Karger, D.R.3
-
20
-
-
20444465355
-
SoapLab-a unified Sesame door to analysis tools
-
Nottingham, UK
-
Senger, M., Rice, P. and Oinn, T. (2003) SoapLab-a unified Sesame door to analysis tools. In Proceedings of the UK e-Science All Hands Meeting 2003, Nottingham, UK.
-
(2003)
Proceedings of the UK E-Science All Hands Meeting 2003
-
-
Senger, M.1
Rice, P.2
Oinn, T.3
-
21
-
-
0345359315
-
Grid: Personalised bioinformatics on the information grid
-
Stevens, R.D., Robinson, A.J. and Goble, C.A. (2003) myGrid: personalised bioinformatics on the information grid. Bioinformatics, 19, i302-i304.
-
(2003)
Bioinformatics
, vol.19
-
-
Stevens, R.D.1
Robinson, A.J.2
Goble, C.A.3
-
22
-
-
0141960163
-
Williams-Beuren syndrome: A challenge for genotype-phenotype correlations
-
Tassabehji, M. (2003) Williams-Beuren syndrome: a challenge for genotype-phenotype correlations. Human Mol. Genet., 12, R229-R237.
-
(2003)
Human Mol. Genet.
, vol.12
-
-
Tassabehji, M.1
-
23
-
-
0033366703
-
Williams syndrome: Use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes
-
Tassabehji, M., Metcalfe, K., Karmiloff-Smith, A., Carette, M., Grant, J., Dennis, N., Reardon, W., Splitt, M., Read, A. and Donnai, D. (1999) Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes. Am. J. Human Genet., 64, 118-125.
-
(1999)
Am. J. Human Genet.
, vol.64
, pp. 118-125
-
-
Tassabehji, M.1
Metcalfe, K.2
Karmiloff-Smith, A.3
Carette, M.4
Grant, J.5
Dennis, N.6
Reardon, W.7
Splitt, M.8
Read, A.9
Donnai, D.10
-
24
-
-
0034306681
-
Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: The low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s)
-
Valero, M., de Luis, O., Cruces, J. and Pérez Jurado,L. (2000) Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s). Genomics, 69, 1-13.
-
(2000)
Genomics
, vol.69
, pp. 1-13
-
-
Valero, M.1
De Luis, O.2
Cruces, J.3
Pérez Jurado, L.4
|