Search "+CODEX"
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- 0.143 + - Copy-number variation
- 0.143 + - Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data
- 0.143 + - CNV calling from NGS data
- 0.143 + - Bioconductor
- 0.143 + - R
- 0.143 + - Exome sequencing
- 0.143 + - CODEX: a normalization and copy number variation detection method for whole exome sequencing
- 0.075 + - ngCGH
- 0.073 + - 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
- 0.067 + - ASCAT
- 0.044 + - Allele-specific copy number profiling by next-generation DNA sequencing
- 0.041 + - saasCNV
- 0.025 + - Genetics in Medicine
- 0.025 + - Python
- 0.025 + - Comparative study of exome copy number variation estimation tools using array comparative genomic hybridization as control
- 0.025 + - Nature Methods
- 0.025 + - Genomics and Precision Medicine
- 0.025 + - Bioinformatics
- 0.025 + - 2015
- 0.025 + - 2017