Pages that link to "Q30361580"

The following pages link to Terrence S. Furey (Q30361580):

Displaying 50 items.

• Initial sequencing and analysis of the human genome (Q21045365) (← links)
• Generation and annotation of the DNA sequences of human chromosomes 2 and 4 (Q21735920) (← links)
• The DNA sequence of human chromosome 7 (Q21735924) (← links)
• The DNA sequence and biology of human chromosome 19 (Q21735933) (← links)
• A physical map of the human genome (Q22122382) (← links)
• Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution (Q22122484) (← links)
• Genome sequence of the Brown Norway rat yields insights into mammalian evolution (Q22122498) (← links)
• Initial sequencing and comparative analysis of the mouse genome (Q22122521) (← links)
• The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC) (Q24307426) (← links)
• The UCSC Genome Browser Database: update 2006 (Q24538714) (← links)
• The accessible chromatin landscape of the human genome (Q24595581) (← links)
• High-resolution genome-wide in vivo footprinting of diverse transcription factors in human cells (Q24614543) (← links)
• DNaseI hypersensitivity at gene-poor, FSH dystrophy-linked 4q35.2 (Q24657535) (← links)
• The human genome browser at UCSC (Q24672361) (← links)
• Knowledge-based analysis of microarray gene expression data by using support vector machines (Q27939386) (← links)
• High-resolution mapping and characterization of open chromatin across the genome (Q28266995) (← links)
• A genome-wide analysis of open chromatin in human tracheal epithelial cells reveals novel candidate regulatory elements for lung function (Q28727907) (← links)
• A predictive framework for integrating disparate genomic data types using sample-specific gene set enrichment analysis and multi-task learning (Q30571667) (← links)
• GSAASeqSP: a toolset for gene set association analysis of RNA-Seq data (Q30850769) (← links)
• Removing reference mapping biases using limited or no genotype data identifies allelic differences in protein binding at disease-associated loci (Q30982599) (← links)
• A hidden Markov random field-based Bayesian method for the detection of long-range chromosomal interactions in Hi-C data. (Q31018961) (← links)
• Support vector machine classification and validation of cancer tissue samples using microarray expression data (Q31835844) (← links)
• Evidence of influence of genomic DNA sequence on human X chromosome inactivation (Q33256101) (← links)
• Identification and characterization of cell type-specific and ubiquitous chromatin regulatory structures in the human genome (Q33294656) (← links)
• F-Seq: a feature density estimator for high-throughput sequence tags (Q33368553) (← links)
• A computational screen for site selective A-to-I editing detects novel sites in neuron specific Hu proteins (Q33521763) (← links)
• Analysis of complex disease association and linkage studies using the University of California Santa Cruz Genome Browser (Q33557518) (← links)
• Both noncoding and protein-coding RNAs contribute to gene expression evolution in the primate brain (Q33730924) (← links)
• A genome-wide analysis of open chromatin in human epididymis epithelial cells reveals candidate regulatory elements for genes coordinating epididymal function (Q33826288) (← links)
• High-resolution mapping studies of chromatin and gene regulatory elements (Q34022627) (← links)
• Open chromatin defined by DNaseI and FAIRE identifies regulatory elements that shape cell-type identity (Q34027627) (← links)
• Heritable individual-specific and allele-specific chromatin signatures in humans (Q34087197) (← links)
• Integration of the cytogenetic map with the draft human genome sequence (Q34191136) (← links)
• Extensive evolutionary changes in regulatory element activity during human origins are associated with altered gene expression and positive selection (Q34325564) (← links)
• Mutational signatures of de-differentiation in functional non-coding regions of melanoma genomes (Q34388520) (← links)
• Novel distal eQTL analysis demonstrates effect of population genetic architecture on detecting and interpreting associations (Q34471686) (← links)
• Global epigenomic analysis of primary human pancreatic islets provides insights into type 2 diabetes susceptibility loci (Q34518460) (← links)
• ChIP-seq and beyond: new and improved methodologies to detect and characterize protein-DNA interactions (Q34644399) (← links)
• Covariation in frequencies of substitution, deletion, transposition, and recombination during eutherian evolution (Q35024015) (← links)
• Genome-wide sequence and functional analysis of early replicating DNA in normal human fibroblasts (Q35225219) (← links)
• Chromatin accessibility mapping identifies mediators of basal transcription and retinoid-induced repression of OTX2 in medulloblastoma (Q35242111) (← links)
• Dynamics of the epigenetic landscape during erythroid differentiation after GATA1 restoration (Q35451782) (← links)
• Integrating genetic and gene expression evidence into genome-wide association analysis of gene sets (Q35694419) (← links)
• MicroRNAs Classify Different Disease Behavior Phenotypes of Crohn's Disease and May Have Prognostic Utility (Q36155959) (← links)
• DeFCoM: analysis and modeling of transcription factor binding sites using a motif-centric genomic footprinter (Q36228906) (← links)
• Chromatin accessibility reveals insights into androgen receptor activation and transcriptional specificity (Q36378106) (← links)
• Comparison of human (and other) genome browsers (Q36388050) (← links)
• New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk (Q36541220) (← links)
• Patterns of regulatory activity across diverse human cell types predict tissue identity, transcription factor binding, and long-range interactions (Q36800430) (← links)
• Comparative recombination rates in the rat, mouse, and human genomes (Q37322300) (← links)