Mattocks C - Search Results

1

AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes.

Dicks E, Teague JW, Stephens P, Raine K, Yates A, Mattocks C, Tarpey P, Butler A, Menzies A, Richardson D, Jenkinson A, Davies H, Edkins S, Forbes S, Gray K, Greenman C, Shepherd R, Stratton MR, Futreal PA, Wooster R. Dicks E, et al. Among authors: mattocks c. Bioinformatics. 2007 Jul 1;23(13):1689-91. doi: 10.1093/bioinformatics/btm152. Epub 2007 May 7. Bioinformatics. 2007. PMID: 17485433 Free PMC article.

2

Comparative sequence analysis.

Mattocks C, Tarpey P, Whittaker J. Mattocks C, et al. Methods Mol Med. 2004;92:115-24. doi: 10.1385/1-59259-432-8:115. Methods Mol Med. 2004. PMID: 14733309 No abstract available.

3

Comparative sequence analysis (CSA): a new sequence-based method for the identification and characterization of mutations in DNA.

Mattocks C, Tarpey P, Bobrow M, Whittaker J. Mattocks C, et al. Hum Mutat. 2000 Nov;16(5):437-43. doi: 10.1002/1098-1004(200011)16:5<437::AID-HUMU9>3.0.CO;2-Q. Hum Mutat. 2000. PMID: 11058902

4

Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11-17 distinct from the GAP related domain.

Mattocks C, Baralle D, Tarpey P, ffrench-Constant C, Bobrow M, Whittaker J. Mattocks C, et al. J Med Genet. 2004 Apr;41(4):e48. doi: 10.1136/jmg.2003.011890. J Med Genet. 2004. PMID: 15060124 Free PMC article. No abstract available.

5

Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer).

Whittaker JL, Mattocks C, Baralle D, Tarpey P, Ffrench-Constant C, Bobrow M. Whittaker JL, et al. Among authors: mattocks c. J Med Genet. 2005 Jun;42(6):e33. J Med Genet. 2005. PMID: 15937073 Free PMC article. No abstract available.

6

Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer).

Whittaker JL, Mattocks C, Baralle D, Tarpey P, ffrench-Constant C, Bobrow M. Whittaker JL, et al. Among authors: mattocks c. J Med Genet. 2005 Jul;42(7):e41. J Med Genet. 2005. PMID: 15994866 Free PMC article. No abstract available.

7

Evaluation of methods to detect CALR mutations in myeloproliferative neoplasms.

Jones AV, Ward D, Lyon M, Leung W, Callaway A, Chase A, Dent CL, White HE, Drexler HG, Nangalia J, Mattocks C, Cross NC. Jones AV, et al. Among authors: mattocks c. Leuk Res. 2015 Jan;39(1):82-7. doi: 10.1016/j.leukres.2014.11.019. Epub 2014 Nov 29. Leuk Res. 2015. PMID: 25499808 Clinical Trial.

8

Semi-automated unidirectional sequence analysis for mutation detection in a clinical diagnostic setting.

Ellard S, Shields B, Tysoe C, Treacy R, Yau S, Mattocks C, Wallace A. Ellard S, et al. Among authors: mattocks c. Genet Test Mol Biomarkers. 2009 Jun;13(3):381-6. doi: 10.1089/gtmb.2008.0096. Genet Test Mol Biomarkers. 2009. PMID: 19405871

9

Genetic diagnosis of familial breast cancer using clonal sequencing.

Morgan JE, Carr IM, Sheridan E, Chu CE, Hayward B, Camm N, Lindsay HA, Mattocks CJ, Markham AF, Bonthron DT, Taylor GR. Morgan JE, et al. Hum Mutat. 2010 Apr;31(4):484-91. doi: 10.1002/humu.21216. Hum Mutat. 2010. PMID: 20127978

10

Interlaboratory diagnostic validation of conformation-sensitive capillary electrophoresis for mutation scanning.

Mattocks CJ, Watkins G, Ward D, Janssens T, Bosgoed EA, van der Donk K, Ligtenberg MJ, Pot B, Theelen J, Cross NC, Scheffer H, Matthijs G. Mattocks CJ, et al. Clin Chem. 2010 Apr;56(4):593-602. doi: 10.1373/clinchem.2009.135426. Epub 2010 Feb 18. Clin Chem. 2010. PMID: 20167696

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