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Pages containing "NCI"
- Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data
- Genetic alterations of triple negative breast cancer by targeted next-generation sequencing and correlation with tumor morphology
- Allele-specific copy number profiling by next-generation DNA sequencing
- MPD: multiplex primer design for next-generation targeted sequencing
- Deep sequencing
- DNA sequencing
- Whole exome sequencing
- Pareto principle
- VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
- Exome sequencing
- Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine
- An integrative approach to reveal driver gene fusions from paired-end sequencing data in cancer
- Principal component analysis
- SAAS-CNV: A Joint Segmentation Approach on Aggregated and Allele Specific Signals for the Identification of Somatic Copy Number Alterations with Next-Generation Sequencing Data
- Genotyping by sequencing
- Analytical and Clinical Validation of a Digital Sequencing Panel for Quantitative, Highly Accurate Evaluation of Cell-Free Circulating Tumor DNA
- An evaluation of copy number variation detection tools from whole-exome sequencing data
- The 80/20 Principle: The Secret to Achieving More with Less
- Digital sequencing
- Nanopore sequencing
- CODEX: a normalization and copy number variation detection method for whole exome sequencing
- Evaluation of somatic copy number estimation tools for whole-exome sequencing data
- Identification of cancer-driver genes in focal genomic alterations from whole genome sequencing data
- Single cell sequencing
- Targeted DNA sequencing
- Opportunities and challenges of whole-genome and -exome sequencing
- Next-Generation Sequencing of Circulating Tumor DNA for Early Cancer Detection
- Principal component analysis reveals the 1000 Genomes Project does not sufficiently cover the human genetic diversity in Asia
- Pyrosequencing
- Comparison of custom capture for targeted next-generation DNA sequencing
- Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals
- Next generation sequencing of triple negative breast cancer to find predictors for chemotherapy response
- San Francisco
- Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller
- Python/asyncio
- Computational methods for detecting copy number variations in cancer genome using next generation sequencing