S. Hughes

发表

The use of whole genome amplification in the study of human disease.

J. Squire, S. Hughes, N. Arneson, 2004, Progress in biophysics and molecular biology.

Modulation by decitabine of gene expression and growth of osteosarcoma U2OS cells in vitro and in xenografts: Identification of apoptotic genes as targets for demethylation

Yuzhuo Wang, J. Squire, J. Bayani, 2007, Cancer Cell International.

Whole Genome Amplification

S. Hughes, S Hughes, 2020, Definitions.

Whole-Genome Amplification by Degenerate Oligonucleotide Primed PCR (DOP-PCR).

Susan Done, R. Houlston, S. Hughes, 2008, CSH protocols.

Increased throughput for fragment analysis on an ABI PRISM 377 automated sequencer using a membrane comb and STRand software.

R J Toonen, S Hughes, S. Hughes, 2001, BioTechniques.

Intrinsic genetic characteristics determine tumor-modifying capacity of fibroblasts: matrix metalloproteinase-3 5A/5A genotype enhances breast cancer cell invasion

R. Walker, S. Hughes, J. Jones, 2007, Breast Cancer Research.

Whole-Genome Amplification by Improved Primer Extension Preamplification PCR (I-PEP-PCR).

R. Houlston, S. Hughes, N. Arneson, 2008, CSH protocols.

Meta-analysis and pooled re-analysis of copy number changes in colorectal cancer detected by comparative genomic hybridization.

R. Houlston, R. Williams, E. Webb, 2006, Anticancer research.

The use of whole genome amplification to study chromosomal changes in prostate cancer: insights into genome-wide signature of preneoplasia associated with cancer progression

A. Evans, R. Houlston, J. Squire, 2006, BMC Genomics.

A method for accurate detection of genomic microdeletions using real-time quantitative PCR

R. Weksberg, A. Bassett, J. Squire, 2005, BMC Genomics.

Microarray comparative genomic hybridisation analysis of intraocular uveal melanomas identifies distinctive imbalances associated with loss of chromosome 3

R. Houlston, I. Giddings, B. Damato, 2005, British Journal of Cancer.

Whole-Genome Amplification by Single-Cell Comparative Genomic Hybridization PCR (SCOMP).

R. Houlston, S. Hughes, N. Arneson, 2008, CSH protocols.

GenomePlex Whole-Genome Amplification.

R. Houlston, S. Hughes, N. Arneson, 2008, CSH protocols.

Use of whole genome amplification and comparative genomic hybridisation to detect chromosomal copy number alterations in cell line material and tumour tissue

J. Squire, J. Bayani, B. Beheshti, 2004, Cytogenetic and Genome Research.

The use of Multiple Displacement Amplified DNA as a control for Methylation Specific PCR, Pyrosequencing, Bisulfite Sequencing and Methylation-Sensitive Restriction Enzyme PCR

S. Hughes, J. Jones, J. Jones, 2007, BMC Molecular Biology.

Matrix Metalloproteinase Single-Nucleotide Polymorphisms and Haplotypes Predict Breast Cancer Progression

S. Duffy, O. Agbaje, S. Hughes, 2007, Clinical Cancer Research.

Genomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arrays.

Richard S Houlston, J. Tolmie, R. Houlston, 2004, Nucleic acids research.

Advances in Nucleic Acid Detection

S. Baker, S. Hughes, J. Gillespie, 2009 .

Association of invasion-promoting tenascin-C additional domains with breast cancers in young women

J. Pringle, R. Walker, S. Hughes, 2010, Breast Cancer Research.

2 Comparative genomic hybridization analysis using metaphase or microarray slides

J. Squire, B. Beheshti, P. Marrano, 2002 .

Use of the QIAGEN GeneReader NGS system for detection of KRAS mutations, validated by the QIAGEN Therascreen PCR kit and alternative NGS platform

Anne-Mette K. Hein, A. Sheridan, Sascha Strauss, 2017, BMC Cancer.

Modulation by decitabine of gene expression and growth of osteosarcoma U2OS cells in vitro and in xenografts: Identification of apoptotic genes as targets for demethylation

Yuzhuo Wang, J. Squire, J. Bayani, 2007, Cancer Cell International.