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Subject Areas on Research
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(Session Introduction) Joint Learning from Multiple Types of Genomic Data
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29 mammalian genomes reveal novel exaptations of mobile elements for likely regulatory functions in the human genome.
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A Bayesian hierarchical model to estimate DNA methylation conservation in colorectal tumors.
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A Decade of CRISPR-Cas Gnome Editing in C. elegans
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A brave new synthetic world. A report of the first meeting on 'Frontiers in Synthetic Biology', Boston, USA, 1-2 December 2008.
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A case study of the reproducibility of transcriptional reporter cell-based RNAi screens in Drosophila.
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A chromosome-level reference genome and pangenome for barn swallow population genomics.
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A course-based research experience: how benefits change with increased investment in instructional time.
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A deletion-generator compound element allows deletion saturation analysis for genomewide phenotypic annotation.
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A draft genome sequence of the elusive giant squid, Architeuthis dux.
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A genetic linkage map of the laboratory rat, Rattus norvegicus.
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A genome end-game: understanding gene function in the nervous system.
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A genome-wide RNAi screen reveals multiple regulators of caspase activation.
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A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p.
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A genome-wide survey of the evolutionarily conserved Wnt pathways in the sea urchin Strongylocentrotus purpuratus.
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A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.
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A genomic regulatory network for development.
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A haplotype-resolved genome assembly of the Nile rat facilitates exploration of the genetic basis of diabetes.
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A high-quality genome and comparison of short- versus long-read transcriptome of the palaearctic duck Aythya fuligula (tufted duck).
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A high-quality, long-read genome assembly of the endangered ring-tailed lemur (Lemur catta).
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A high-resolution map of human evolutionary constraint using 29 mammals.
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A methodology for utilization of predictive genomic signatures in FFPE samples.
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A new duck genome reveals conserved and convergently evolved chromosome architectures of birds and mammals.
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A new emu genome illuminates the evolution of genome configuration and nuclear architecture of avian chromosomes.
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A physical map of the mouse genome.
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A recombinational portrait of the Drosophila pseudoobscura genome.
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A sampling of methods to study chromosome and genome structure and function.
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A sea urchin genome project: sequence scan, virtual map, and additional resources.
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A unique role of the DNA fragmentation factor in maintaining genomic stability.
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ATAC-ing the mechanisms of renin regulation.
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Absence of a simple code: how transcription factors read the genome.
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Adaptive Radiation Genomics of Two Ecologically Divergent Hawai'ian Honeycreepers: The 'akiapōlā'au and the Hawai'i 'amakihi.
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Advances in targeted genome editing.
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Advancing toxicology research using in vivo high throughput toxicology with small fish models.
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Alu Insertion Polymorphisms as Evidence for Population Structure in Baboons.
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An Arabidopsis thaliana lipoxygenase gene can be induced by pathogens, abscisic acid, and methyl jasmonate.
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An SSLP marker-anchored BAC framework map of the mouse genome.
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An algorithm for the reconstruction of consensus sequences of ancient segmental duplications and transposon copies in eukaryotic genomes.
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An encyclopedia of mouse DNA elements (Mouse ENCODE).
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An ensemble model of competitive multi-factor binding of the genome.
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An improved germline genome assembly for the sea lamprey Petromyzon marinus illuminates the evolution of germline-specific chromosomes.
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Ancient bacterial endosymbionts of insects: Genomes as sources of insight and springboards for inquiry.
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Animals in a bacterial world, a new imperative for the life sciences.
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Applications of high-throughput RNA interference screens to problems in cell and developmental biology.
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Avian Binocularity and Adaptation to Nocturnal Environments: Genomic Insights from a Highly Derived Visual Phenotype.
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Avian genomes. A flock of genomes. Introduction.
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Avianbase: a community resource for bird genomics.
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Balancing selection maintains hyper-divergent haplotypes in Caenorhabditis elegans.
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Bayesian genome- and epigenome-wide association studies with gene level dependence.
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Bone-associated gene evolution and the origin of flight in birds.
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Breed Differences in Dog Cognition Associated with Brain-Expressed Genes and Neurological Functions.
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CRISPR Library Screening in Cultured Cardiomyocytes.
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CRISPR-Cas9-Guided Genome Engineering in C. elegans.
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Caenorhabditis elegans DNA mismatch repair gene msh-2 is required for microsatellite stability and maintenance of genome integrity.
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Capturing the primordial Kras mutation initiating urethane carcinogenesis.
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Carbon sequestration in Synechococcus Sp.: from molecular machines to hierarchical modeling.
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Caspase-3 promotes genetic instability and carcinogenesis.
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ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia.
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Chromatin and DNA replication.
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Chromosomal-Level Genome Assembly of the Sea Urchin Lytechinus variegatus Substantially Improves Functional Genomic Analyses.
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Chromosome-Level Reference Genomes for Two Strains of Caenorhabditis briggsae: An Improved Platform for Comparative Genomics.
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Comparative RNA sequencing reveals substantial genetic variation in endangered primates.
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Comparative embryology without a microscope: using genomic approaches to understand the evolution of development.
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Comparative genome sequencing of Drosophila pseudoobscura: chromosomal, gene, and cis-element evolution.
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Comparative genomics reveals insights into avian genome evolution and adaptation.
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Comparing reference-based RNA-Seq mapping methods for non-human primate data.
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Complete genomic screen for disease susceptibility loci in nuclear families.
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Complexity reduction in context-dependent DNA substitution models.
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Composition and dynamics of the Caenorhabditis elegans early embryonic transcriptome.
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Computational analysis of core promoters in the Drosophila genome.
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Consequences of recombination rate variation on quantitative trait locus mapping studies. Simulations based on the Drosophila melanogaster genome.
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Conservation of dynamic characteristics of transcriptional regulatory elements in periodic biological processes.
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Convergent and divergent evolution of genomic imprinting in the marsupial Monodelphis domestica.
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Convergent evolution of chicken Z and human X chromosomes by expansion and gene acquisition.
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Convergent evolution of chromosomal sex-determining regions in the animal and fungal kingdoms.
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Coordinated genome-wide modifications within proximal promoter cis-regulatory elements during vertebrate evolution
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Core and region-enriched networks of behaviorally regulated genes and the singing genome.
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Cross species genomic analysis identifies a mouse model as undifferentiated pleomorphic sarcoma/malignant fibrous histiocytoma.
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DNA-remethylation around a STAT5-binding enhancer in the alphaS1-casein promoter is associated with abrupt shutdown of alphaS1-casein synthesis during acute mastitis.
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DNase-seq: a high-resolution technique for mapping active gene regulatory elements across the genome from mammalian cells.
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Darwinian genomics and diversity in the tree of life.
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De novo PacBio long-read and phased avian genome assemblies correct and add to reference genes generated with intermediate and short reads.
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Defining origins of replication in mammalian cells.
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Detecting differential copy number variation between groups of samples.
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Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.
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Developmental roles of pufferfish Hox clusters and genome evolution in ray-fin fish.
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Dissection of a quantitative trait locus for PR interval duration identifies Tnni3k as a novel modulator of cardiac conduction.
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Drosophila muller f elements maintain a distinct set of genomic properties over 40 million years of evolution.
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Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.
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Early low-titer neutralizing antibodies impede HIV-1 replication and select for virus escape.
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Earth BioGenome Project: Sequencing life for the future of life.
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EchinoDB, an application for comparative transcriptomics of deeply-sampled clades of echinoderms.
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Editing the Epigenome: Reshaping the Genomic Landscape.
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Editing the Neuronal Genome: a CRISPR View of Chromatin Regulation in Neuronal Development, Function, and Plasticity.
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Effects of Space Flight on Mouse Liver versus Kidney: Gene Pathway Analyses.
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Effects of glutathione on chromium-induced DNA crosslinking and DNA polymerase arrest.
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Effects of inversions on within- and between-species recombination and divergence.
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Efficient Genome Editing in Caenorhabditis elegans with a Toolkit of Dual-Marker Selection Cassettes.
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Efficient Genome-Wide Sequencing and Low-Coverage Pedigree Analysis from Noninvasively Collected Samples.
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Endosymbiont evolution: predictions from theory and surprises from genomes.
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Endosymbiosis: lessons in conflict resolution.
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Epigenome characterization at single base-pair resolution.
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Epigenomics of centromere assembly and function.
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Evaluation of the genomic extent of effects of fixed inversion differences on intraspecific variation and interspecific gene flow in Drosophila pseudoobscura and D. persimilis.
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Evidence for GC-biased gene conversion as a driver of between-lineage differences in avian base composition.
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Evidence for a single loss of mineralized teeth in the common avian ancestor.
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Evidence for multiple loci from a genome scan of autism kindreds.
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Evolution. CNCing is believing.
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Evolutionary and biomedical insights from a marmoset diploid genome assembly.
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Evolutionary and ecological functional genomics.
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Evolutionary and phylogenetic insights from a nuclear genome sequence of the extinct, giant, "subfossil" koala lemur Megaladapis edwardsi.
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Evolutionary genetics and acclimatization in nephrology.
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F-Seq: a feature density estimator for high-throughput sequence tags.
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False gene and chromosome losses in genome assemblies caused by GC content variation and repeats.
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From disease ontology to disease-ontology lite: statistical methods to adapt a general-purpose ontology for the test of gene-ontology associations.
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Functional analysis of novel SNPs and mutations in human and mouse genomes.
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Functional organization of the genome may shape the species boundary in the house mouse.
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GREAT improves functional interpretation of cis-regulatory regions.
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GWAS analyzer: integrating genotype, phenotype and public annotation data for genome-wide association study analysis.
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Gene conversion and linkage: effects on genome evolution and speciation.
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Gene loss, adaptive evolution and the co-evolution of plumage coloration genes with opsins in birds.
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Gene-environment regulatory circuits of right ventricular pathology in tetralogy of fallot.
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General olfactory sensitivity database (GOSdb): candidate genes and their genomic variations.
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Generalized dead-end elimination algorithms make large-scale protein side-chain structure prediction tractable: implications for protein design and structural genomics.
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Genetic and genomic evolution of sexual reproduction: echoes from LECA to the fungal kingdom.
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Genome accessibility is widely preserved and locally modulated during mitosis.
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Genome annotation assessment in Drosophila melanogaster.
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Genome editing: the end of the beginning.
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Genome evolution in an insect cell: distinct features of an ant-bacterial partnership.
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Genome-editing Technologies for Gene and Cell Therapy.
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Genome-scale functional genomics identify genes preferentially essential for multiple myeloma cells compared to other neoplasias.
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Genome-wide activity-dependent MeCP2 phosphorylation regulates nervous system development and function.
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Genome-wide analysis of STAT target genes: elucidating the mechanism of STAT-mediated oncogenesis.
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Genome-wide analysis of heat stress-stimulated transposon mobility in the human fungal pathogen Cryptococcus deneoformans.
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Genome-wide identification of autosomal genes with allelic imbalance of chromatin state.
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Genome-wide identification of calcium-response factor (CaRF) binding sites predicts a role in regulation of neuronal signaling pathways.
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Genome-wide identification of regulatory elements in Sertoli cells.
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Genome-wide meta-analyses identify multiple loci associated with smoking behavior.
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Genome-wide patterns of expression in Drosophila pure species and hybrid males.
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Genome-wide prediction of imprinted murine genes.
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Genome-wide scan reveals signatures of selection related to pollution adaptation in non-model estuarine Atlantic killifish (Fundulus heteroclitus).
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Genomic abnormalities of the murine model of Fabry disease after disease-related perturbation, a systems biology approach.
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Genomic and functional variation of human centromeres.
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Genomic determination of the glucocorticoid response reveals unexpected mechanisms of gene regulation.
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Genomic mismatch scanning: a new approach to genetic linkage mapping.
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Genomic prediction of locoregional recurrence after mastectomy in breast cancer.
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Genomic predictors of the maximal O₂ uptake response to standardized exercise training programs.
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Genomic sequence and expression of a cloned human carbonyl reductase gene with daunorubicin reductase activity.
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Genomic signatures of G-protein-coupled receptor expansions reveal functional transitions in the evolution of cephalopod signal transduction.
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Genomic signatures of near-extinction and rebirth of the crested ibis and other endangered bird species.
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Gfastats: conversion, evaluation and manipulation of genome sequences using assembly graphs.
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Globally Relaxed Selection and Local Adaptation in Boechera stricta.
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Great ape genetic diversity and population history.
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Guidelines for Genome-Scale Analysis of Biological Rhythms.
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Haplotype-resolved assembly of diploid genomes without parental data.
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Heterochromatic sequences in a Drosophila whole-genome shotgun assembly.
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Hi-C scaffolded short- and long-read genome assemblies of the California sea lion are broadly consistent for syntenic inference across 45 million years of evolution.
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High-resolution genome-wide in vivo footprinting of diverse transcription factors in human cells.
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Human apolipoprotein E2, E3, and E4 isoform-specific transgenic mice: human-like pattern of glial and neuronal immunoreactivity in central nervous system not observed in wild-type mice.
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Hybrid de novo genome assembly and centromere characterization of the gray mouse lemur (Microcebus murinus).
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Hypertension and albuminuria in chronic kidney disease mapped to a mouse chromosome 11 locus.
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Identification of novel mediators of NF-kappaB through genome-wide survey of monocyte adherence-induced genes.
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Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.
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Identification of variants in CNGA3 as cause for achromatopsia by exome sequencing of a single patient.
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Identifying branch-specific positive selection throughout the regulatory genome using an appropriate proxy neutral.
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Identifying gene regulatory elements by genome-wide recovery of DNase hypersensitive sites.
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Impact of Conditioning Intensity and Genomics on Relapse After Allogeneic Transplantation for Patients With Myelodysplastic Syndrome.
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Incorporation of a horizontally transferred gene into an operon during cnidarian evolution.
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Induction of an immortalized songbird cell line allows for gene characterization and knockout by CRISPR-Cas9.
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Induction of internucleosomal DNA fragmentation by carcinogenic chromate: relationship to DNA damage, genotoxicity, and inhibition of macromolecular synthesis.
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Infectious pathogen detection arrays: viral detection in cell lines and postmortem brain tissue.
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Initial sequencing and comparative analysis of the mouse genome.
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Initiation of the Primate Genome Project.
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Integrative genomic approaches identify IKBKE as a breast cancer oncogene.
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Interpreting the genomic landscape of speciation: a road map for finding barriers to gene flow.
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Intraspecific phylogenetic congruence among multiple symbiont genomes.
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Intraspecific variation in symbiont genomes: bottlenecks and the aphid-buchnera association.
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Intrinsic and cyclin-dependent kinase-dependent control of spindle pole body duplication in budding yeast.
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Inversions shape the divergence of Drosophila pseudoobscura and Drosophila persimilis on multiple timescales.
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Jumping at the chance for precise DNA integration.
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Less is more: compact genomes pay dividends.
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Lichens.
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Lineage-specific expansions provide genomic complexity among sea urchin GTPases.
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Little qualitative RNA misexpression in sterile male F1 hybrids of Drosophila pseudoobscura and D. persimilis.
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Loss of a histone deacetylase dramatically alters the genomic distribution of Spo11p-catalyzed DNA breaks in Saccharomyces cerevisiae.
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Low frequency of paleoviral infiltration across the avian phylogeny.
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Mechanistic insights into cancer cell killing through interaction of phosphodiesterase 3A and schlafen family member 12.
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Mechanotransduction Mechanisms for Intraventricular Diastolic Vortex Forces and Myocardial Deformations: Part 2.
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Merfin: improved variant filtering, assembly evaluation and polishing via k-mer validation.
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Metagenomic and small-subunit rRNA analyses reveal the genetic diversity of bacteria, archaea, fungi, and viruses in soil.
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Mimulus is an emerging model system for the integration of ecological and genomic studies
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Mismatch repair proteins and mitotic genome stability.
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Mitochondrial DNA polymorphism A4917G is independently associated with age-related macular degeneration.
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Modelling the effects of age-related mtDNA mutation accumulation; complex I deficiency, superoxide and cell death.
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Molecular biologist's guide to proteomics.
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Molecular genetics of successful smoking cessation: convergent genome-wide association study results.
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Morphological and genomic shifts in mole-rat 'queens' increase fecundity but reduce skeletal integrity.
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Motif composition, conservation and condition-specificity of single and alternative transcription start sites in the Drosophila genome.
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Multiplex CRISPR/Cas9-based genome editing for correction of dystrophin mutations that cause Duchenne muscular dystrophy.
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Multiplex CRISPR/Cas9-based genome engineering from a single lentiviral vector.
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Murine noroviruses comprising a single genogroup exhibit biological diversity despite limited sequence divergence.
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NAFLD is associated with methylation shifts with relevance for the expression of genes involved in lipoprotein particle composition.
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Nonconsensus Protein Binding to Repetitive DNA Sequence Elements Significantly Affects Eukaryotic Genomes.
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Novel Insights into Chromosome Evolution in Birds, Archosaurs, and Reptiles.
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Nucleosome Turnover Regulates Histone Methylation Patterns over the Genome.
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Olfactory Receptor Subgenomes Linked with Broad Ecological Adaptations in Sauropsida.
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On a Special Collection in MMBR on Sex in Fungi: Molecular Mechanisms and Evolutionary Implications.
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Organization and evolution of a gene-rich region of the mouse genome: a 12.7-Mb region deleted in the Del(13)Svea36H mouse.
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Organizing mRNA export.
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OrthoClusterDB: an online platform for synteny blocks.
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Overlapping high-resolution copy number alterations in cancer genomes identified putative cancer genes in hepatocellular carcinoma.
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Palo: spatially aware color palette optimization for single-cell and spatial data.
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Parrot Genomes and the Evolution of Heightened Longevity and Cognition.
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Participant choices for return of genomic results in the eMERGE Network.
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Pedigree-based and phylogenetic methods support surprising patterns of mutation rate and spectrum in the gray mouse lemur.
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Perspectives from the Avian Phylogenomics Project: Questions that Can Be Answered with Sequencing All Genomes of a Vertebrate Class.
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Phylogenomic analyses data of the avian phylogenomics project.
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Platypus and echidna genomes reveal mammalian biology and evolution.
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Polyploidy: A Biological Force From Cells to Ecosystems.
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Population genomics reveal recent speciation and rapid evolutionary adaptation in polar bears.
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Predicting Alzheimer's Disease Using Combined Imaging-Whole Genome SNP Data.
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Predicting cell-type-specific gene expression from regions of open chromatin.
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Preface.
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Progressive Cactus is a multiple-genome aligner for the thousand-genome era.
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Prospective estimation of recombination signal efficiency and identification of functional cryptic signals in the genome by statistical modeling.
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PseudoBase: a genomic visualization and exploration resource for the Drosophila pseudoobscura
subgroup.
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Pulling the genome in opposite directions to dissect gene networks.
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RTK and TGF-beta signaling pathways genes in the sea urchin genome.
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RUNX1 maintains the identity of the fetal ovary through an interplay with FOXL2.
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Radiation-induced genomic instability: radiation quality and dose response.
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Rapid behavioral and genomic responses to social opportunity.
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Recent advances in genome editing and creation of genetically modified pigs.
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Recombination rate variation in closely related species.
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Recombination-Aware Phylogenomics Reveals the Structured Genomic Landscape of Hybridizing Cat Species.
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Recombining without Hotspots: A Comprehensive Evolutionary Portrait of Recombination in Two Closely Related Species of Drosophila.
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Reference genome and demographic history of the most endangered marine mammal, the vaquita.
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Regulatory gene networks and the properties of the developmental process.
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Replicated Landscape Genomics Identifies Evidence of Local Adaptation to Urbanization in Wood Frogs.
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Response to Comment on "Whole-genome analyses resolve early branches in the tree of life of modern birds".
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Returning integrated genomic risk and clinical recommendations: The eMERGE study.
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Revising messages traveling along the cellular information superhighway.
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Ribonucleoprotein infrastructure regulating the flow of genetic information between the genome and the proteome.
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Saving the Patent Law from Itself: Informal Remarks Concerning the Systemic Problems Afflicting Developed Intellectual Property Regimes
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Selection against admixture and gene regulatory divergence in a long-term primate field study.
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Sequencing studies in human genetics: design and interpretation.
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Sequencing three crocodilian genomes to illuminate the evolution of archosaurs and amniotes.
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Serial analysis of gene expression (SAGE) in normal human trabecular meshwork.
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Shrinkage estimation for robust and efficient screening of single-SNP association from case-control genome-wide association studies.
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Site frequency spectra from genomic SNP surveys.
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Six reference-quality genomes reveal evolution of bat adaptations.
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Spatial organization of the mammalian genome surveillance machinery in response to DNA strand breaks.
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Stability selection for regression-based models of transcription factor-DNA binding specificity.
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Statistical Viewer: a tool to upload and integrate linkage and association data as plots displayed within the Ensembl genome browser.
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Stochastic segment models of eukaryotic promoter regions.
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The BLUEPRINT Data Analysis Portal.
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The DNA methylation landscape of advanced prostate cancer.
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The Genome 10K Project: a way forward.
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The NIEHS TaRGET II Consortium and environmental epigenomics.
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The Nuclear Pore Complex in Cell Type-Specific Chromatin Structure and Gene Regulation.
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The Role of EBV-Induced Hypermethylation in Gastric Cancer Tumorigenesis.
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The challenge and promise of estimating the de novo mutation rate from whole-genome comparisons among closely related individuals.
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The contribution of admixture to primate evolution.
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The correlation of copy number variations with longevity in a genome-wide association study of Han Chinese.
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The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies.
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The effects of nucleotide substitution model assumptions on estimates of nonparametric bootstrap support.
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The era of reference genomes in conservation genomics.
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The evolutionary significance of cis-regulatory mutations.
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The expanding implications of polyploidy.
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The forkhead transcription factor FoxI1 remains bound to condensed mitotic chromosomes and stably remodels chromatin structure.
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The genome of a songbird.
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The genome of the green anole lizard and a comparative analysis with birds and mammals.
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The genome of the sea urchin Stongylocentrotus purpuratus
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The genomic consequences of adaptive divergence and reproductive isolation between species of manakins.
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The genomic underpinnings of apoptosis in Strongylocentrotus purpuratus.
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The hard clam genome reveals massive expansion and diversification of inhibitors of apoptosis in Bivalvia.
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The histone modification pattern of active genes revealed through genome-wide chromatin analysis of a higher eukaryote.
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The invertebrate deuterostomes: an introduction to their phylogeny, reproduction, development, and genomics.
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The people behind the papers - Yingxi Cao, Ken Poss and Jingli Cao.
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The small subunit of the mammalian mitochondrial ribosome. Identification of the full complement of ribosomal proteins present.
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The tardigrade Hypsibius dujardini, a new model for studying the evolution of development.
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The western painted turtle genome, a model for the evolution of extreme physiological adaptations in a slowly evolving lineage.
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Three crocodilian genomes reveal ancestral patterns of evolution among archosaurs.
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Three periods of regulatory innovation during vertebrate evolution.
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Truncating BRCA1 mutations are uncommon in a cohort of hereditary prostate cancer families with evidence of linkage to 17q markers.
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Tumor necrosis factor-alpha and tumor growth factor-beta1 genotype: partial association with intragraft gene expression in two cases of long-term peripheral tolerance to a kidney transplant.
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Two types of recombination hotspots in bacteriophage T4: one requires DNA damage and a replication origin and the other does not.
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Uncovering the HARbingers of human brain evolution.
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Unlocking the secrets of the genome.
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Using Phylogenomic Data to Explore the Effects of Relaxed Clocks and Calibration Strategies on Divergence Time Estimation: Primates as a Test Case.
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Visual annotation of the gene database.
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Whole genome analysis: experimental access to all genome sequenced segments through larger-scale efficient oligonucleotide synthesis and PCR.
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Whole genome expression profiling of normal human fetal and adult ocular tissues.
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Whole-Genome Identification, Phylogeny, and Evolution of the Cytochrome P450 Family 2 (CYP2) Subfamilies in Birds.
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Whole-genome analyses resolve early branches in the tree of life of modern birds.
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Why sequence all eukaryotes?
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Widespread false gene gains caused by duplication errors in genome assemblies.
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Keywords of People
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Ferreira, Paulo Alexandre,
Associate Professor in Ophthalmology,
Pathology
-
Fox, Donald T,
Associate Professor of Pharmacology & Cancer Biology,
Duke Science & Society
-
Gordan, Raluca Mihaela,
Associate Professor in Biostatistics & Bioinformatics,
Computer Science
-
Hartemink, Alexander J.,
Professor in the Department of Computer Science,
Biology
-
Liu, Yutao,
Adjunct Assistant Professor in the Department of Medicine,
Medicine, Medical Genetics
-
Pitt, Geoffrey Stuart,
Adjunct Professor in the Department of Medicine,
Medicine, Cardiology
-
Reddy, Timothy E,
Associate Professor of Biostatistics & Bioinformatics,,
Molecular Genetics and Microbiology
-
Sullivan, Beth Ann,
Professor of Molecular Genetics and Microbiology,
Duke Science & Society
-
Wray, Gregory Allan,
Professor of Biology,
Evolutionary Anthropology