Search "+FISH"
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- 0.500 + - Epigenetics in Human Disease
- 0.500 + - Comparative genomic hybridization
- 0.392 + - ngCGH
- 0.263 + - Copy-number variation
- 0.154 + - Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data
- 0.024 + - CODEX: a normalization and copy number variation detection method for whole exome sequencing
- 0.020 + - Allele-specific copy number
- 0.016 + - The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups
- 0.013 + - Gene expression
- 0.011 + - PennCNV
- 0.011 + - Computational methods for detecting copy number variations in cancer genome using next generation sequencing
- 0.011 + - Cattle
- 0.011 + - GenomeStudio
- 0.008 + - Genomics and Precision Medicine
- 0.006 + - Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data
- 0.005 + - CBS
- 0.005 + - Genetic alterations of triple negative breast cancer by targeted next-generation sequencing and correlation with tumor morphology
- 0.005 + - Tumorscape
- 0.005 + - Amplicon
- 0.005 + - CoNIFER