| Item Type | Name |
|
Concept
|
Amino Acid Sequence
|
|
Concept
|
Base Sequence
|
|
Concept
|
Oncogenes
|
|
Concept
|
Multigene Family
|
|
Concept
|
Molecular Sequence Data
|
|
Concept
|
Genome
|
|
Concept
|
Genes, Essential
|
|
Concept
|
Genes, Tumor Suppressor
|
|
Concept
|
Genomic Library
|
|
Concept
|
Sequence Analysis, DNA
|
|
Concept
|
Genome, Insect
|
|
Concept
|
Genetic Pleiotropy
|
|
Concept
|
Exome
|
|
Concept
|
Oligonucleotide Array Sequence Analysis
|
|
Concept
|
High-Throughput Nucleotide Sequencing
|
|
Concept
|
Regulatory Elements, Transcriptional
|
|
Concept
|
Open Reading Frames
|
|
Concept
|
Genome, Fungal
|
|
Concept
|
Genome, Human
|
|
Concept
|
Transcriptome
|
|
Concept
|
Molecular Sequence Annotation
|
|
Concept
|
Genes, Fungal
|
|
Concept
|
Sequence Analysis, RNA
|
|
Concept
|
Polymorphism, Single Nucleotide
|
|
Concept
|
Quantitative Trait Loci
|
|
Concept
|
Genetic Loci
|
|
Academic Article
|
Integrative Array Analyzer: a software package for analysis of cross-platform and cross-species microarray data.
|
|
Academic Article
|
Integrative missing value estimation for microarray data.
|
|
Academic Article
|
A graph-based approach to systematically reconstruct human transcriptional regulatory modules.
|
|
Academic Article
|
Mining coherent dense subgraphs across massive biological networks for functional discovery.
|
|
Academic Article
|
Bayesian approach to transforming public gene expression repositories into disease diagnosis databases.
|
|
Academic Article
|
Gene Aging Nexus: a web database and data mining platform for microarray data on aging.
|
|
Academic Article
|
An integrative approach to characterize disease-specific pathways and their coordination: a case study in cancer.
|
|
Academic Article
|
Integrating many co-splicing networks to reconstruct splicing regulatory modules.
|
|
Academic Article
|
Unraveling complex temporal associations in cellular systems across multiple time-series microarray datasets.
|
|
Academic Article
|
Integrative analysis of many weighted co-expression networks using tensor computation.
|
|
Academic Article
|
Dense chromatin activates Polycomb repressive complex 2 to regulate H3 lysine 27 methylation.
|
|
Academic Article
|
Zooming in on genome organization.
|
|
Academic Article
|
Automated multidimensional phenotypic profiling using large public microarray repositories.
|
|
Academic Article
|
Functional annotation and network reconstruction through cross-platform integration of microarray data.
|
|
Academic Article
|
Integrative disease classification based on cross-platform microarray data.
|
|
Academic Article
|
Joint genome-wide profiling of miRNA and mRNA expression in Alzheimer's disease cortex reveals altered miRNA regulation.
|
|
Academic Article
|
The genetic architecture of gene expression levels in wild baboons.
|
|
Academic Article
|
High-resolution functional annotation of human transcriptome: predicting isoform functions by a novel multiple instance-based label propagation method.
|
|
Academic Article
|
Integrative analysis of many RNA-seq datasets to study alternative splicing.
|
|
Academic Article
|
A panel of induced pluripotent stem cells from chimpanzees: a resource for comparative functional genomics.
|
|
Academic Article
|
CancerDetector: ultrasensitive and non-invasive cancer detection at the resolution of individual reads using cell-free DNA methylation sequencing data.
|
|
Academic Article
|
Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis.
|
|
Academic Article
|
ARG-SHINE: improve antibiotic resistance class prediction by integrating sequence homology, functional information and deep convolutional neural network.
|
|
Academic Article
|
cfTrack: A Method of Exome-Wide Mutation Analysis of Cell-free DNA to Simultaneously Monitor the Full Spectrum of Cancer Treatment Outcomes Including MRD, Recurrence, and Evolution.
|
|
Academic Article
|
Cost-effective methylome sequencing of cell-free DNA for accurately detecting and locating cancer.
|
|
Academic Article
|
cfSNV: a software tool for the sensitive detection of somatic mutations from cell-free DNA.
|