Pages that link to "Q40572619"

The following pages link to High-resolution single-nucleotide polymorphism array and clustering analysis of loss of heterozygosity in human lung cancer cell lines (Q40572619):

Displaying 48 items.

• Virtual karyotyping with SNP microarrays reduces uncertainty in the diagnosis of renal epithelial tumors (Q21203678) (← links)
• Inferring loss-of-heterozygosity from unpaired tumors using high-density oligonucleotide SNP arrays (Q21563517) (← links)
• Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumors (Q24643365) (← links)
• The application of single nucleotide polymorphism microarrays in cancer research (Q24653582) (← links)
• CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays (Q25257143) (← links)
• Biomarkers in cancer staging, prognosis and treatment selection (Q28278305) (← links)
• Genome wide SNP comparative analysis between EGFR and KRAS mutated NSCLC and characterization of two models of oncogenic cooperation in non-small cell lung carcinoma (Q28385454) (← links)
• Characterization of a naturally occurring breast cancer subset enriched in epithelial-to-mesenchymal transition and stem cell characteristics (Q28751743) (← links)
• A novel technique for measuring variations in DNA copy-number: competitive genomic polymerase chain reaction (Q30479759) (← links)
• High-resolution copy number analysis of paraffin-embedded archival tissue using SNP BeadArrays. (Q33271277) (← links)
• Genome-wide analysis of neuroblastomas using high-density single nucleotide polymorphism arrays (Q33275966) (← links)
• Using expression arrays for copy number detection: an example from E. coli (Q33287803) (← links)
• SNPExpress: integrated visualization of genome-wide genotypes, copy numbers and gene expression levels (Q33316565) (← links)
• Genome coverage and sequence fidelity of phi29 polymerase-based multiple strand displacement whole genome amplification (Q33978394) (← links)
• High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPs (Q34106761) (← links)
• Identification of chromosome arm 9p as the most frequent target of homozygous deletions in lung cancer (Q34444611) (← links)
• Clonality of the stem cell compartment during evolution of myelodysplastic syndromes and other bone marrow failure syndromes (Q34635314) (← links)
• Whole genome SNP arrays as a potential diagnostic tool for the detection of characteristic chromosomal aberrations in renal epithelial tumors. (Q34745214) (← links)
• Genome-wide loss of heterozygosity and copy number alteration in esophageal squamous cell carcinoma using the Affymetrix GeneChip Mapping 10 K array (Q35205608) (← links)
• Microsatellite analysis of pleural supernatants could increase sensitivity of pleural fluid cytology (Q35836697) (← links)
• Emerging strategies and applications of pharmacogenomics (Q35988130) (← links)
• The two single nucleotide polymorphisms in the H37/RBM5 tumour suppressor gene at 3p21.3 correlated with different subtypes of non-small cell lung cancers (Q36128798) (← links)
• Novel technology and the development of pharmacogenetics within the pharmaceutical industry (Q36186950) (← links)
• High-throughput molecular analysis in lung cancer: insights into biology and potential clinical applications (Q36288148) (← links)
• Advancement in characterization of genomic alterations for improved diagnosis, treatment and prognostics in cancer (Q36344108) (← links)
• Loss of heterozygosity analyzed by single nucleotide polymorphism array in cancer (Q36373263) (← links)
• Using high-throughput SNP technologies to study cancer (Q36426758) (← links)
• The progress on genetic analysis of nasopharyngeal carcinoma (Q36445020) (← links)
• Application of oligonucleotide arrays to high-content genetic analysis (Q36481133) (← links)
• The affymetrix GeneChip platform: an overview (Q36580114) (← links)
• Loss of heterozygosity and copy number abnormality in clear cell renal cell carcinoma discovered by high-density affymetrix 10K single nucleotide polymorphism mapping array (Q36730935) (← links)
• Genome-wide DNA copy number analysis in pancreatic cancer using high-density single nucleotide polymorphism arrays (Q36802303) (← links)
• Oligonucleotide arrays for high-resolution analysis of copy number alteration in mental retardation/multiple congenital anomalies (Q36943647) (← links)
• Genomic investigation of alpha-synuclein multiplication and parkinsonism (Q37362778) (← links)
• Large-scale genomic analysis of ovarian carcinomas (Q37453861) (← links)
• Genomewide scan for loss of heterozygosity and chromosomal amplification in breast carcinoma using single-nucleotide polymorphism arrays (Q37678142) (← links)
• Use of SNPs in cancer predisposition analysis, diagnosis and prognosis: tools and prospects. (Q38089070) (← links)
• High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumor (Q38301206) (← links)
• Whole genome SNP arrays using DNA derived from formalin-fixed, paraffin-embedded ovarian tumor tissue (Q38441304) (← links)
• LOHAS: loss-of-heterozygosity analysis suite (Q39612693) (← links)
• Whole-genome profiling of chromosomal aberrations in hepatoblastoma using high-density single-nucleotide polymorphism genotyping microarrays (Q40013719) (← links)
• High resolution analysis of non-small cell lung cancer cell lines by whole genome tiling path array CGH. (Q40368368) (← links)
• High-resolution whole-organ mapping with SNPs and its significance to early events of carcinogenesis. (Q40420797) (← links)
• Reconstruction of an integrated genome-scale co-expression network reveals key modules involved in lung adenocarcinoma (Q43095950) (← links)
• Genome-wide screening of loci associated with drug resistance to 5-fluorouracil-based drugs (Q51917708) (← links)
• Molecular karyotyping of human hepatocellular carcinoma using single-nucleotide polymorphism arrays (Q51939495) (← links)
• Are there any more ovarian tumor suppressor genes? A new perspective using ultra high-resolution copy number and loss of heterozygosity analysis. (Q53383644) (← links)
• Relationship between the genetic expression of WTAP and bladder cancer and patient prognosis. (Q64975026) (← links)