The page is empty.
Incoming Links #
Codes Written (Code 0) #
- Flutter
- HOMER
- Mesos
- MongoDB
- MySQL
- NCBI Genome Workbench
- Octopus
- PARADIGM
- Ray (assembler)
- STAR
- VCFtools
Related Codes (Code 1) #
Pages starting with "C++"
- Caffeine
- Central limit theorem
- cBioPortal
- Cell differentiation
- Cytokeratin
- CNVkit
- CLC Genomics Workbench
- ClinVar
- Cafestol
- CD44
- Cytokine release syndrome
- CFD
- Cattle
- Chronic myelogenous leukemia
- Circa
- Cell growth
- Clustering
- COPS5
- Cytotoxic T cell
- Cambridge
- Celery
- Cecilia Payne
- Carcinogenesis
- Cloud computing
- Cluster analysis
- Copenhagen
- Cell cycle
- Computational epigenetics
- C
- custom.css
- Cancer stem cell
- Colon cancer
- CD
- CR
- CCLE
- Charles Darwin
- CVD
- Cytogenomic array
- Chromatin
- CIViC
- Cretaceous–Paleogene extinction event
- Circular binary segmentation
- CD20
- Comparative genomic hybridization
- Carl Sagan
- CGHub
- Coronary artery disease
- .config
- CDISC
- CTGS
- The cancer genome
- Computer crime
- cffDNA
- CDK12 Inhibition Reverses De Novo and Acquired PARP Inhibitor Resistance in BRCA Wild-Type and Mutated Models of Triple-Negative Breast Cancer
- Cardiovascular disease
- Cone cell
- CoNIFER
- Cellular senescence
- CML
- Cell proliferation
- CMS
- Cyclin D1
- Cell-free tumor DNA
- COX1
- Cytochrome c
- Cosmos: A Spacetime Odyssey
- custom.js
- Chemotherapy
- CDK12
- Canis lupus familiaris
- Cystic fibrosis
- Clair Cameron Patterson
- Colorectal cancer
- CDKN2A
- Citric acid cycle
- cyvcf2
- ChIP-seq
- CummeRbund
- Crestor
- Chicken
- Cisplatin
- Chromothripsis
- Convolutional neural network
- Chi-squared test
- cutadapt
- Complex landscapes of somatic rearrangement in human breast cancer genomes
- Chromosome
- Cancer-specific defects in DNA repair pathways as targets for personalized therapeutic approaches
- Companion diagnostic
- Cancer panel
- Cosmos
- Cytoscape Web
- Cas9
- CPT1A
- ConSig
- Counsyl
- Complex disease and phenotype mapping in the domestic dog
- CaVEMan
- Conda
- Cetacea
- Coronavirus disease 2019
- COSMIC
- Cataract
- CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer
- Comparative assessment of methods for the fusion transcripts detection from RNA-Seq data
- ClusterCall
- Cancer genomics
- Cancer immunotherapy
- CNV
- CNA
- Cytokine
- Chimeric antigen receptor
- Contact
- Computational fluid dynamics
- CYCS
- Complex plane
- CODEX: a normalization and copy number variation detection method for whole exome sequencing
- CAC
- Cambrian explosion
- CanineHD Whole-Genome Genotyping BeadChip
- Chromosome conformation capture
- CRISPR
- Cell signalling
- Chimpanzee
- Cadherin-1
- CDH1
- ChatGPT
- Canis familiaris
- Cytoscape
- Cancer
- Calorie restriction
- Cerebral infarct
- Cross-site request forgery
- The Cancer Genome Atlas
- Cobimetinib
- Clinical trial
- COTA
- Cytochrome c oxidase subunit I
- Charles Lee
- Consciousness
- CD274
- Cell signaling
- Classification
- CBS
- Cow
- Continuous integration
- Connectome
- CFTR
- CUPS
- Cyclooxygenase
- Concrete Mathematics
- Childcare
- Challenges in analysis and interpretation of microsatellite data for population genetic studies
- Cython
- Content management system
- CAR-T
- Characterizing genomic alterations in cancer by complementary functional associations
- CCND1
- Chromosome instability
- Common cold
- CloudNeo
- Comprehensive functional analysis of the tousled-like kinase 2 frequently amplified in aggressive luminal breast cancers
- CODEX
- Copy-number variation
- Comprehensive molecular portraits of human breast tumours
- Crohn's disease
- Cancer genomics: from discovery science to personalized medicine
- CTNNB1
- COVID-19
- CRKRS
- Central nervous system
- Computer security
- Cat
- Cholesterol
- Cufflinks
- CGH
- CSC
- Cancer genome data analysis and knowledgebase
- Cytoscape.js
- Cancer epigenetics
- Coursera
- CNV calling from NGS data
- ctDNA
- Cancer Genomics Hub
- CRC
- Computer vision
- Comparison of custom capture for targeted next-generation DNA sequencing
- Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data
- Colaboratory
- Chevrolet Impala
- CIN
- CDx
- Covalent modifications of histones during development and disease pathogenesis
- Cell-free fetal DNA
- Cancer Target Gene Screening: a web application for breast cancer target gene screening using multi-omics data analysis
- CentOS
- Cooking
- Cross-correlation
- Copy number
- ChIP-PED
- Conditional expectation
- CSRF
- Computational methods for detecting copy number variations in cancer genome using next generation sequencing
Pages ending with "C++"
- APOBEC
- METABRIC
- MOOC
- ICGC
- APC
- IHEC
- Gleevec
- TNBC
- HDAC
- Propositional logic
- AUC
- Receiver operating characteristic
- Trimmomatic
- HMEC
- GDC
- MCMC
- ROC
- Hyungyong Kim/.vimrc
- SurvivalROC
- ExAC
- First-order logic
- NABIC
- GDISC
- AsciiDoc
- 3C
- GISTIC
- NVC
- PIC
- MYC
- glibc
- Nymphomaniac
- MHC
- Insilicogen, Inc.
- Word2vec
- Antibiotic
- Trac
- PoC
- Apple Inc.
- DVC
- Music
- NSCLC
- iPSC
Pages containing "C++"
- Oncogene
- Bioconda
- Epigenome-wide association studies
- Quantum computing
- Lung cancer
- DNA-PKcs
- Structural variation
- PIK3CA
- Welch's t-test
- MUC1
- Statistical inference
- Google Genomics
- Homologous recombination
- Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data
- Lincomycin
- Mathematical model
- Analysis of East Asia genetic substructure using genome-wide SNP arrays
- Octopus
- Jaccard index
- TCGA
- ngCGH
- Genetic alterations of triple negative breast cancer by targeted next-generation sequencing and correlation with tumor morphology
- Mockup
- MERS-CoV
- Molecular and genetic properties of tumors associated with local immune cytolytic activity
- Genome-wide association study
- Panoramic radiographs
- Nonviolent Communication
- Docker
- Ring species
- Feature extraction
- Friedrich Nietzsche
- Induced pluripotent stem cell
- GWAS Catalog
- Sequence analysis of mutations and translocations across breast cancer subtypes
- Database of Genomic Variants archive
- Dental caries
- Allele-specific copy number profiling by next-generation DNA sequencing
- Docker Swarm
- Neutrocyte
- MPD: multiplex primer design for next-generation targeted sequencing
- Hacker
- Deep sequencing
- Genome project
- ASCAT
- Replication timing
- SSCP
- Synthetic lethality
- Stack Overflow
- Human leukocyte antigen
- Hepatocellular carcinoma
- Digital healthcare
- Hepatic cancer
- Science and religion
- Evolution: A Course for Educators
- GCI
- Beta-catenin
- Blue Collar Bioinformatics
- Identification of Biomarkers for Breast Cancer Using Databases
- Ethyl alcohol
- Journal of Animal Breeding and Genomics
- Secretary problem
- User experience
- DECIPHER
- Metabolomics
- An Introduction To Applied Bioinformatics
- Michaelis–Menten kinetics
- Machine learning
- DNA sequencing
- Oracle
- NK cell
- A GWAS assessment of the contribution of genomic imprinting to the variation of body mass index in mice
- Squamous cell carcinoma
- OncoLand
- Pipeline for Bioinformatics
- VCF
- Receptor tyrosine kinase
- The Descent of Man, and Selection in Relation to Sex
- Probabilistic Programming and Bayesian Methods for Hackers
- Senescence-associated secretory phenotype
- Anaconda
- Biological Sequence Analysis
- Reference-guided alignment
- Executive Decision
- ASCN
- Natural language processing
- RT-PCR
- Genetically modified organism
- Phenomics
- Support vector machine
- NCBI Insights
- Identification of druggable cancer driver genes amplified across TCGA datasets
- HMGCR
- Ecology
- patch
- Workflow description language
- Stem cell
- Microsatellite
- X-inactivation
- Triple-negative breast cancer: an unmet medical need
- Oncotarget
- Sexual reproduction
- The life history of 21 breast cancers
- GNU C Library
- MEDICI: Mining Essentiality Data to Identify Critical Interactions for Cancer Drug Target Discovery and Development
- Job crafting
- Mycobacterium tuberculosis
- Text-to-speech
- Biomarkers in triple negative breast cancer: A review
- BCR
- Lynch syndrome
- Ecogwiki를 이용한 지식정보관리
- A mutational signature in gastric cancer suggests therapeutic strategies
- Advanced Linux Programming
- Gut microbiota
- Glycemic load
- Long non-coding RNA
- Genomic Data Commons
- Standard score
- VIPER: Visualization Pipeline for RNA-seq, a Snakemake workflow for efficient and complete RNA-seq analysis
- Intelligence quotient
- ECM1
- Supercritical fluid
- Data Analysis and Statistical Inference
- Practical guidelines for the comprehensive analysis of ChIP-seq data
- Multidimensional scaling
- RECOMB 2001
- PennCNV
- Quadratic programming
- DECIPHER (database)
- Single-strand conformation polymorphism
- Oncotator
- DNA mismatch repair
- Bitcoin
- Jacques Monod
- Drug repurposing: progress, challenges and recommendations
- Landscape of somatic mutations in 560 breast cancer whole-genome sequences
- Environment-wide association study
- Inbreeding coefficient
- Mathematical modelling of infectious disease
- Polycomb-group proteins
- lncRNA
- scikit-learn
- Lab color space
- VarScan
- Blockchain
- Pathway Interaction Database
- PyCon Korea 2014 “DNA 데이터로 가족찾기” 발표 후기
- Genetic algorithm
- SCF
- saasCNV
- Oncogenesis
- Internationalization and localization
- 8 Steps to a Pain-Free Back
- Therapeutic opportunities within the DNA damage response
- Transcript-level expression analysis of RNA-seq experiments with HISAT, StringTie and Ballgown
- Hackers and Painters
- Nothing's Gonna Change My Love for You
- Personalized medicine
- Reinforcement learning
- Logistic regression
- Bevacizumab
- Warburg effect
- Metagenomics - a guide from sampling to data analysis
- Autisum spectrum disorder
- Search engine optimization
- Rocks
- Regulatory T cell
- Sonic hedgehog
- Linear discriminant analysis
- JARID1B is a luminal lineage-driving oncogene in breast cancer
- Live in another country
- Whole exome sequencing
- Allele-specific copy number
- Epigenetics in Human Disease
- Paclitaxel
- Meta-analysis of the global gene expression profile of triple-negative breast cancer identifies genes for the prognostication and treatment of aggressive breast cancer
- Elasticsearch
- ABCC11
- V(D)J recombination
- Scale-free network
- Pelvic organ prolapse
- pVAC-Seq
- Economic democracy
- Samsung Electronics
- Javascript
- Pareto principle
- Michaelis–Menten equation
- Natural killer cell
- VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
- Prognostic value of PDL1 expression in pancreatic cancer
- bcbio-nextgen
- Bechy's law
- Database encryption
- Exome sequencing
- 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
- PCA
- Kickstarter
- E-cadherin
- Genomics and Precision Medicine
- Genetic drift
- Dynamic programming
- Functional programming
- Richard Dawkins
- Decision tree
- An integrative approach to reveal driver gene fusions from paired-end sequencing data in cancer
- Principal component analysis
- Pancreatic cancer
- Apocrine
- Expression quantitative trait loci
- The landscape of somatic copy-number alteration across human cancers
- Oxford Nanopore Technologies
- Single nucleotide variation
- Statistical hypothesis test
- qPCR
- Acute myeloid leukemia
- Object-oriented programming
- 1000 Genomes Project
- Suppressor T cell
- Best linear unbiased prediction
- Gene Set Enrichment Analysis
- Microbiome
- Human genetic variation database, a reference database of genetic variations in the Japanese population
- False discovery rate
- Prostate cancer
- T cell
- Glycemic index
- Reverse transcription polymerase chain reaction
- James Clerk Maxwell
- Ecogwiki sites
- Retrospective
- Genetic alterations of histone lysine methyltransferases and their significance in breast cancer
- Naver Corporation
- Markov chain Monte Carlo
- NCBI Genome Workbench
- Krebs cycle
- Magnetic resonance imaging
- z-score
- HMG-CoA reductase
- Nicotinamide mononucleotide
- Growth factor
- Ovarian cancer
- Becoming a Technical Leader
- GTPase-activating protein
- 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
- Bonferroni correction
- Monoclonal antibody
- Reactive programming
- Methods of integrating data to uncover genotype–phenotype interactions
- Breast cancer epigenetics: from DNA methylation to microRNAs
- Knowledge information management using Ecogwiki
- Single cell
- Medicine
- The Price of Everything
- Triple-negative breast cancer
- Localization
- Bayesian inference
- Gene Essentiality Profiling Reveals Gene Networks and Synthetic Lethal Interactions with Oncogenic Ras
- Genotyping by sequencing
- Genomic Selection in Aquaculture: Application, Limitations and Opportunities With Special Reference to Marine Shrimp and Pearl Oysters
- ResearchGate
- Antimicrobial resistance
- Speciation
- The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups
- Black hole
- Great Permian Extinction
- Practical Business Python
- Lysergic acid diethylamide
- Notch signaling pathway
- Human Genome Project
- Explainable artificial intelligence
- scRNA-seq
- Paracetamol
- Frederick Sanger
- Precision medicine
- T lymphocyte
- Embryonic development
- SARS-CoV-2
- A high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studies
- Natural selection
- Stomach cancer
- Non-negative matrix factorization
- AscatNgs
- Genomic imprinting
- Smyd3 Is a Transcriptional Potentiator of Multiple Cancer-Promoting Genes and Required for Liver and Colon Cancer Development
- The Scale of the Universe
- Liver cancer
- European Genome-phenome Archive
- Directed acyclic graph
- Data Analysis for Genomics
- Graphical model
- OMICStools
- Impact factor
- Genetics
- Erwin Schrödinger
- Genetic distance
- Robust relationship inference in genome-wide association studies
- Syndecan-2
- FinTech
- Predicting cancer-specific vulnerability via data-driven detection of synthetic lethality
- 5 Centimeters Per Second
- Oncotator: cancer variant annotation tool
- Systemic lupus erythematosus
- Endoplasmic reticulum
- Gene-environment interaction
- Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data
- Mutational processes molding the genomes of 21 breast cancers
- Analytical and Clinical Validation of a Digital Sequencing Panel for Quantitative, Highly Accurate Evaluation of Cell-Free Circulating Tumor DNA
- PCDHGA12
- An evaluation of copy number variation detection tools from whole-exome sequencing data
- Physics
- Singular value decomposition
- Scikit Flow
- Dendritic cell
- Microsatellite instability
- Genomics of Drug Sensitivity in Cancer
- Tumorscape
- WHSC1L1
- Histone acetylation
- Amplicon
- Ethics
- Attach on Titan
- Polygenic score
- Epidermal growth factor receptor
- Histone modification
- Rhesus macaque
- DNAcopy
- 제22회 KOBIC 차세대 생명정보학 교육 워크샵
- SciPy 2018
- Artificial intelligence
- The 80/20 Principle: The Secret to Achieving More with Less
- Factor analysis
- Digital sequencing
- Selective sweep
- Beta blocker
- Genetic variation
- Sus scrofa
- Low back pain
- Attention deficit hyperactivity disorder
- Nutritional genomics
- Personal health record
- An integrative somatic mutation analysis to identify pathways linked with survival outcomes across 19 cancer types
- GeomicMating
- PyTorch
- Targeted genes by ChIP-seq
- Epithelial–mesenchymal transition
- Mathematics
- Polymorphic information content
- Oriental medicine
- Edge computing
- Epigenetics
- Traditional Korean medicine
- Estrogen receptor
- Herceptin
- TimescaleDB
- Notch
- Brad Chapman
- Jinwoo Choi
- Nanopore sequencing
- Lymphocyte
- X-Men: First Class
- Genetic Variation and Diseases
- International Cancer Genome Consortium
- ACE2
- Why We Get Sick
- schema.org
- Bioconductor
- Plate tectonics
- Histone code
- Oncogenomics
- MCF-7
- Genetic testing
- Biochip
- Pathway and network analysis of cancer genomes
- DuckDB
- Brain cancer
- Sickle-cell disease
- Microsatellite instability in colorectal cancer
- Foundation Medicine
- Bioinformatics
- De novo transcriptome assembly
- Epigenomics
- Felis catus
- Hackers: Heroes of the Computer Revolution
- Google Analytics
- ENCODE
- Helicobacter pylori
- 구글 앱 엔진에서 Ecogwiki 과도한 과금 문제 해결
- Drug Discovery in Cancer Epigenetics
- Angiotensin-converting enzyme
- Semantic data integration for toxicogenomic laboratory experiment management systems
- django CMS
- Patterns of somatic mutation in human cancer genomes
- District 9
- Genetic fingerprinting
- Hereditary nonpolyposis colorectal cancer
- Immune checkpoint
- Sequence Read Archive
- ACE inhibitor
- Alcohol flush reaction
- Evaluation of somatic copy number estimation tools for whole-exome sequencing data
- Science fiction
- Granger causality
- The Impact of Mutations in SARS-CoV-2 Spike on Viral Infectivity and Antigenicity
- Analysis of variance
- macOS
- Sequence assembly
- Gentamicin
- 2019-nCoV
- Genomic selection
- Amazon Web Services
- Wellcome Trust Sanger Institute
- PCR
- Data Analysis for Life Sciences
- Locust
- MkDocs
- Data science
- Scopes Trial
- PyCon Korea 2014
- PyCon Korea 2015
- Alcohol
- PyCon Korea 2018
- Evaluation of Transfer Learning with Deep Convolutional Neural Networks for Screening Osteoporosis in Dental Panoramic Radiographs
- Identification of cancer-driver genes in focal genomic alterations from whole genome sequencing data
- Array CGH
- The BioPAX community standard for pathway data sharing
- F-statistics
- Non-receptor tyrosine kinase
- Rapamycin
- Single cell sequencing
- GenoLogics
- Synthetic biology
- Nucleotide excision repair
- Genetic risk index
- Monte Carlo tree search
- DOT1L cooperates with the c-Myc-p300 complex to epigenetically derepress CDH1 transcription factors in breast cancer progression
- Role of RBP2-Induced ER and IGF1R-ErbB Signaling in Tamoxifen Resistance in Breast Cancer
- BRCA2
- Feature selection
- Quantum mechanics
- GenesWell BCT
- Machine learning for Genomics
- BRCA
- The dynamics of the piglet gut microbiome during the weaning transition in association with health and nutrition
- TCR
- Geographic coordinate system
- Tuberculosis
- Statistical hypothesis testing
- Apple Watch
- Human Mammary Epithelial Cells
- Gene set enrichment
- Objective and key results
- Speech synthesis
- Targeted DNA sequencing
- Ultima Genomics
- Extrachromosomal DNA
- Sokcho
- Entrez Direct
- Minkowski distance
- Genomic portrait of resectable hepatocellular carcinomas: implications of RB1 and FGF19 aberrations for patient stratification
- Fecal microbiota transplant
- Jackson Pollock
- Multi-omics
- Opportunities and challenges of whole-genome and -exome sequencing
- Permian–Triassic extinction event
- Metagenomics
- PrognoScan
- Genetic risk score
- Vitamin D receptor
- BCL1
- BCL2
- MuTect
- Robbins and Cotran Pathologic Basis of Disease
- Unicode
- Mercurial
- Nuclear magnetic resonance
- The Skeptical Environmentalist
- falcon
- Reactome
- Next-Generation Sequencing of Circulating Tumor DNA for Early Cancer Detection
- Antagonistic pleiotropy hypothesis
- PCGF2
- Secret Lab of a Mad Scientist
- Fundamental interaction
- Real-time polymerase chain reaction
- Artificial neural network
- Sexual selection
- Loss-of-function variant
- Evolutionary psychology
- T cell receptor
- Enhancer
- VCFtools
- Special relativity
- Drug discovery
- ACE
- My Cancer Genome
- Translational bioinformatics
- Proof of concept
- BCL11A
- Philadelphia chromosome
- Michael Faraday
- B-cell
- Flynn effect
- Microchimerism
- Parallel computing
- BCL11A is a triple-negative breast cancer gene with critical functions in stem and progenitor cells
- Headache
- Histone acetyltransferase
- Inclusive fitness
- Post-translational modification
- Principal component analysis reveals the 1000 Genomes Project does not sufficiently cover the human genetic diversity in Asia
- UCSC Genome Browser
- PodCast
- Functional reactive programming
- PyClone
- Keyczar
- Digital PCR
- Microbiota
- Genomics
- Electromagnetism
- G protein-coupled receptor
- Marker-assisted selection
- Feedback
- Population genetics
- Gel electrophoresis
- BRCA1
- ncRNA
- Richard M. Durbin
- Euclidean distance
- PyCon US 2013
- Real-time PCR
- Gut microbiome
- University of Cambridge
- RNA interference
- Decimal degrees
- Identity by descent
- Ice age
- Homologous recombination deficiency
- Accel World
- Global transcription network incorporating distal regulator binding reveals selective cooperation of cancer drivers and risk genes
- Slack
- Bioinformatics problems
- Tuxedo protocol
- Python for Scientists
- Alopecia areata
- Statistics
- Magnetic field
- International Human Epigenome Consortium
- Michael Stratton
- Gattaca
- Is the future of personalized therapy in triple-negative breast cancer based on molecular subtype
- Granulocyte
- Non-coding RNA
- Histone deacetylase
- Fisher's exact test
- Biological network
- Killer-cell immunoglobulin-like receptor
- Django Channels
- Genetic network
- Distributed computing
- Alternative splicing
- MEL-18 loss mediates estrogen receptor–α downregulation and hormone independence
- Thyroid cancer
- EquineSNP50 BeadChip
- PDCD5
- Urinary tract infection
- PyScript
- Breast cancer
- SCNA
- Pyrosequencing
- Scopes Monkey Trial
- Warbug effect
- Pathogen surveillance
- Pioneer factor
- Extracellular vesicle
- Tumor suppressor SET9 guides the epigenetic plasticity of breast cancer cells and serves as an early-stage biomarker for predicting metastasis
- GNU Screen
- T-score
- Docker Compose
- Intracranial hemorrhage
- Adoptive T-cell therapy
- Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
- k-means clustering
- Gradient descent
- Ecogwiki
- Genetic composite index
- B cell
- The topography of mutational processes in breast cancer genomes
- Polymerase chain reaction
- BCIP
- Google Cloud Platform
- Mark Zuckerberg
- 人CoDom
- Biological pathway
- microRNA
- MapReduce
- Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals
- Ascorbic acid
- Polycystic kidney disease
- DECIPHER (software)
- Podcast
- Testis-determining factor
- Polycomb regulates mesoderm cell fate-specification in embryonic stem cells through activation and repression mechanisms
- Somatic evolution in cancer
- SNV calling from NGS data
- Quantitative trait loci
- AACR
- Small-cell lung carcinoma
- Base excision repair
- Next generation sequencing of triple negative breast cancer to find predictors for chemotherapy response
- Mechanisms underlying mutational signatures in human cancers
- GCTA
- 장고(Django) QueryDict 사용 주의
- scikit-image
- Polygenic risk score
- BioHackers
- Miss Peregrine's Home for Peculiar Children
- Image processing
- San Francisco
- Major histocompatibility complex
- A framework for organizing cancer-related variations from existing databases, publications and NGS data using a High-performance Integrated Virtual Environment (HIVE)
- Inception
- Database of Genomic Variants
- The Structure of Scienfitic Revolution
- LOD score
- Recurrent neural network
- Kinetochore
- Vincent van Gogh
- Glycosylation
- Scala
- Identification of gene-drug interactions that impact patient survival in TCGA
- Excel
- Naive Bayes classifier
- Apache Jena
- Acetaminophen
- Identical by state
- Dactinomycin
- Gene duplication
- Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller
- 제33회 KOBIC 차세대 생명정보학 교육 워크샵
- Web Intelligence and Big Data
- The 26th International KOGO Annual Conference
- Wolf Children
- Science
- DNA barcoding
- Electronic health record
- TCA cycle
- Macrogen
- Detoxification
- Noam Chomsky
- Precocious puberty
- β-catenin
- Structural biology
- Python/asyncio
- A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns
- Structure
- MACS
- Expectation maximization
- SciPy