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- Epigenome-wide association studies
- Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data
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- Genetic alterations of triple negative breast cancer by targeted next-generation sequencing and correlation with tumor morphology
- Molecular and genetic properties of tumors associated with local immune cytolytic activity
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- MPD: multiplex primer design for next-generation targeted sequencing
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- Genome-wide association study identifies 74 loci associated with educational attainment
- Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine
- Genomics and Precision Medicine
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- 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
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- Genomic Selection in Aquaculture: Application, Limitations and Opportunities With Special Reference to Marine Shrimp and Pearl Oysters
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- A high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studies
- Genomic imprinting
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- Predicting cancer-specific vulnerability via data-driven detection of synthetic lethality
- Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data
- 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
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- 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
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- Identification of cancer-driver genes in focal genomic alterations from whole genome sequencing data
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- The dynamics of the piglet gut microbiome during the weaning transition in association with health and nutrition
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- Genomic portrait of resectable hepatocellular carcinomas: implications of RB1 and FGF19 aberrations for patient stratification
- Opportunities and challenges of whole-genome and -exome sequencing
- Next-Generation Sequencing of Circulating Tumor DNA for Early Cancer Detection
- Secret Lab of a Mad Scientist
- Artificial neural network
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- Characterizing genomic alterations in cancer by complementary functional associations
- Principal component analysis reveals the 1000 Genomes Project does not sufficiently cover the human genetic diversity in Asia
- Cancer genomics: from discovery science to personalized medicine
- Decimal degrees
- Homologous recombination deficiency
- Python for Scientists
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- Alternative splicing
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- Tumor suppressor SET9 guides the epigenetic plasticity of breast cancer cells and serves as an early-stage biomarker for predicting metastasis
- Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
- Comparison of custom capture for targeted next-generation DNA sequencing
- BCIP
- Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals
- Ascorbic acid
- DECIPHER (software)
- Polycomb regulates mesoderm cell fate-specification in embryonic stem cells through activation and repression mechanisms
- Small-cell lung carcinoma
- Base excision repair
- Next generation sequencing of triple negative breast cancer to find predictors for chemotherapy response
- scikit-image
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- The Structure of Scienfitic Revolution
- Dactinomycin
- Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller
- Science
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- Computational methods for detecting copy number variations in cancer genome using next generation sequencing