-
2
-
-
84951574833
-
-
European Cytogenetic Guidelines January 2012 Available at. (last accessed 16 January
-
European Cytogenetic Guidelines: ECA Newsletter, January 2012. Available at. http://e-c-a.eu/files/downloads/E.C.A.-General-Guidelines-Version%202.0.pdf (last accessed 16 January 2015)
-
(2015)
ECA Newsletter
-
-
-
4
-
-
84892821784
-
On behalf of the ESHG Quality committee: Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic) (2013)
-
Claustres M, Koz?ich V, Dequeker E et al. on behalf of the ESHG Quality committee: Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic) (2013). Eur J Hum Genet 2013; 22: 160-170
-
(2013)
Eur J Hum Genet
, Issue.22
, pp. 160-170
-
-
Claustres, M.1
Kozich, V.2
Dequeker, E.3
-
6
-
-
84951573733
-
-
Available at. last accessed 16 January
-
European co-operation for accreditation: Available at. http://www.european-accreditation.org/ (last accessed 16 January 2015)
-
(2015)
European Co-operation for Accreditation
-
-
-
7
-
-
84951574834
-
-
Available at. UK NEQAS Executive Office last accessed 16 January
-
UK NEQAS Executive Office: Sheffield S10 2PB. Available at. http://www.ukneqas.org.uk/ (last accessed 16 January 2015)
-
(2015)
Sheffield S10 2PB
-
-
-
8
-
-
84856797441
-
CGH arrays compared for DNA isolated from formalin-fixed, paraffin-embedded material
-
Krijgsman O, Israeli D, Haan JC et al. CGH arrays compared for DNA isolated from formalin-fixed, paraffin-embedded material. Genes Chromosomes Cancer 2012; 51: 344-352
-
(2012)
Genes Chromosomes Cancer
, vol.51
, pp. 344-352
-
-
Krijgsman, O.1
Israeli, D.2
Haan, J.C.3
-
9
-
-
84907761755
-
Performance of amplicon-based next generation DNA sequencing for diagnostic gene mutation profiling in oncopathology
-
Sie D, Snijders PJ, Meijer GA et al. Performance of amplicon-based next generation DNA sequencing for diagnostic gene mutation profiling in oncopathology. Cell Oncol (Dordr) 2014; 37: 353-361
-
(2014)
Cell Oncol (Dordr)
, vol.37
, pp. 353-361
-
-
Sie, D.1
Snijders, P.J.2
Meijer, G.A.3
-
10
-
-
84875077830
-
Comparison of targeted next-generation sequencing (NGS) and real-time PCR in the detection of EGFR, KRAS, and BRAF mutations on formalin-fixed, paraffin-embedded tumor material of non-small cell lung carcinoma-superiority of NGS
-
Tuononen K, Mäki-Nevala S, Sarhadi VK et al. Comparison of targeted next-generation sequencing (NGS) and real-time PCR in the detection of EGFR, KRAS, and BRAF mutations on formalin-fixed, paraffin-embedded tumor material of non-small cell lung carcinoma-superiority of NGS. Genes Chromosomes Cancer 2013; 52: 503-511
-
(2013)
Genes Chromosomes Cancer
, vol.52
, pp. 503-511
-
-
Tuononen, K.1
Mäki-Nevala, S.2
Sarhadi, V.K.3
-
12
-
-
7444228551
-
Analysis of HER-2/neu amplification in endometrial carcinoma by chromogenic in situ hybridization Correlation with fluorescence in situ hybridization, HER-2/neu, p53 and Ki-67 protein expression, and outcome
-
Peiró G, D Mayr DHillemanns P et al. Analysis of HER-2/neu amplification in endometrial carcinoma by chromogenic in situ hybridization. Correlation with fluorescence in situ hybridization, HER-2/neu, p53 and Ki-67 protein expression, and outcome. Mod Pathol 2004; 17: 277-287
-
(2004)
Mod Pathol
, vol.17
, pp. 277-287
-
-
Peiró, G.1
Mayr DHillemanns, P.D.2
-
14
-
-
84905962250
-
Focal chromosomal copy number aberrations in cancer-Needles in a genome haystack
-
Krijgsman O, Carvalho B, Meijer GA, Steenbergen RD, Ylstra B. Focal chromosomal copy number aberrations in cancer-Needles in a genome haystack. Biochim Biophys Acta 2014; 1843: 2698-2704
-
(2014)
Biochim Biophys Acta
, vol.1843
, pp. 2698-2704
-
-
Krijgsman, O.1
Carvalho, B.2
Meijer, G.A.3
Steenbergen, R.D.4
Ylstra, B.5
-
15
-
-
84877072617
-
Detection limits of DNA copy number alterations in heterogeneous cell populations
-
Krijgsman O, Israeli D, Van Essen HF et al. Detection limits of DNA copy number alterations in heterogeneous cell populations. Cell Oncol (Dordr) 2013; 36: 27-36
-
(2013)
Cell Oncol (Dordr)
, vol.36
, pp. 27-36
-
-
Krijgsman, O.1
Israeli, D.2
Van Essen, H.F.3
-
16
-
-
84964240053
-
Biological and therapeutic impact of intratumor heterogeneity in cancer evolution
-
McGranahan N, Swanton C. Biological and therapeutic impact of intratumor heterogeneity in cancer evolution. Cancer Cell 2015; 27: 15-26
-
(2015)
Cancer Cell
, vol.27
, pp. 15-26
-
-
McGranahan, N.1
Swanton, C.2
-
17
-
-
84922273986
-
Targeted sequencing by proximity ligation for comprehensive variant detection and local haplotyping
-
De Vree PJ, De Wit E, Yilmaz M et al. Targeted sequencing by proximity ligation for comprehensive variant detection and local haplotyping. Nat Biotechnol 2014; 32: 1019-1025
-
(2014)
Nat Biotechnol
, vol.32
, pp. 1019-1025
-
-
De Vree, P.J.1
De Wit, E.2
Yilmaz, M.3
-
19
-
-
84913590291
-
DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly
-
Scheinin I, Sie D, Bengtsson H et al. DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly. Genome Res 2014; 24: 2022-2032
-
(2014)
Genome Res
, vol.24
, pp. 2022-2032
-
-
Scheinin, I.1
Sie, D.2
Bengtsson, H.3
-
21
-
-
84884533830
-
Reflecting on earlier experiences with unsolicited findings: Points to consider for next-generation sequencing and informed consent in diagnostics
-
Rigter T, Henneman L, Kristoffersson U et al. Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics. Hum Mutat 2013; 34: 1322-1328
-
(2013)
Hum Mutat
, vol.34
, pp. 1322-1328
-
-
Rigter, T.1
Henneman, L.2
Kristoffersson, U.3
-
22
-
-
84883198965
-
Technical and implementation issues in using next-generation sequencing of cancers in clinical practice
-
Ulahannan D, Kovac MB, Mulholland PJ, Cazier J-B, Tomlinson I. Technical and implementation issues in using next-generation sequencing of cancers in clinical practice. Br J Cancer 2013; 109: 827-835
-
(2013)
Br J Cancer
, vol.109
, pp. 827-835
-
-
Ulahannan, D.1
Kovac, M.B.2
Mulholland, P.J.3
Cazier, J.-B.4
Tomlinson, I.5
-
23
-
-
84905828163
-
Next generation sequencing and tumor mutation profiling: Are we ready for routine use in the oncology clinic?
-
Tripathy D, Harnden K, Kimberly Blackwell K, Robson M. Next generation sequencing and tumor mutation profiling: are we ready for routine use in the oncology clinic?. BMC Med 2014; 12: 140 (http://www.biomedcentral.com/1741-7015/12/140/-ins1)
-
(2014)
BMC Med
, vol.12
, pp. 140
-
-
Tripathy, D.1
Harnden, K.2
Kimberly Blackwell, K.3
Robson, M.4
-
24
-
-
65549156891
-
International consensus for neuroblastoma molecular diagnostics: Report from the International Neuroblastoma Risk Group (INRG) Biology Committee
-
Ambros PF, Ambros IM, Brodeur GM et al. International consensus for neuroblastoma molecular diagnostics: report from the International Neuroblastoma Risk Group (INRG) Biology Committee. Br J Cancer 2009; 100: 1471-1482
-
(2009)
Br J Cancer
, vol.100
, pp. 1471-1482
-
-
Ambros, P.F.1
Ambros, I.M.2
Brodeur, G.M.3
-
26
-
-
84890254448
-
Recommendations for human epidermal growth factor receptor 2 testing in breast cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Update
-
Wolff AC, Hammond MEH, Hicks DG et al. Recommendations for human epidermal growth factor receptor 2 testing in breast cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Update. J Clin Oncol 2013; 31: 3997-4014
-
(2013)
J Clin Oncol
, vol.31
, pp. 3997-4014
-
-
Wolff, A.C.1
Meh, H.2
Hicks, D.G.3
|