about
Initial sequencing and analysis of the human genomeGeneration and annotation of the DNA sequences of human chromosomes 2 and 4The DNA sequence of human chromosome 7The DNA sequence and biology of human chromosome 19A physical map of the human genomeSequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolutionGenome sequence of the Brown Norway rat yields insights into mammalian evolutionInitial sequencing and comparative analysis of the mouse genomeThe status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)The UCSC Genome Browser Database: update 2006The accessible chromatin landscape of the human genomeHigh-resolution genome-wide in vivo footprinting of diverse transcription factors in human cellsDNaseI hypersensitivity at gene-poor, FSH dystrophy-linked 4q35.2The human genome browser at UCSCKnowledge-based analysis of microarray gene expression data by using support vector machinesHigh-resolution mapping and characterization of open chromatin across the genomeA genome-wide analysis of open chromatin in human tracheal epithelial cells reveals novel candidate regulatory elements for lung functionA predictive framework for integrating disparate genomic data types using sample-specific gene set enrichment analysis and multi-task learningGSAASeqSP: a toolset for gene set association analysis of RNA-Seq dataRemoving reference mapping biases using limited or no genotype data identifies allelic differences in protein binding at disease-associated loci.A hidden Markov random field-based Bayesian method for the detection of long-range chromosomal interactions in Hi-C data.Support vector machine classification and validation of cancer tissue samples using microarray expression data.Evidence of influence of genomic DNA sequence on human X chromosome inactivationIdentification and characterization of cell type-specific and ubiquitous chromatin regulatory structures in the human genome.F-Seq: a feature density estimator for high-throughput sequence tags.A computational screen for site selective A-to-I editing detects novel sites in neuron specific Hu proteins.Analysis of complex disease association and linkage studies using the University of California Santa Cruz Genome Browser.Both noncoding and protein-coding RNAs contribute to gene expression evolution in the primate brainA genome-wide analysis of open chromatin in human epididymis epithelial cells reveals candidate regulatory elements for genes coordinating epididymal function.High-resolution mapping studies of chromatin and gene regulatory elementsOpen chromatin defined by DNaseI and FAIRE identifies regulatory elements that shape cell-type identity.Heritable individual-specific and allele-specific chromatin signatures in humans.Integration of the cytogenetic map with the draft human genome sequence.Extensive evolutionary changes in regulatory element activity during human origins are associated with altered gene expression and positive selection.Mutational signatures of de-differentiation in functional non-coding regions of melanoma genomes.Novel distal eQTL analysis demonstrates effect of population genetic architecture on detecting and interpreting associationsGlobal epigenomic analysis of primary human pancreatic islets provides insights into type 2 diabetes susceptibility loci.ChIP-seq and beyond: new and improved methodologies to detect and characterize protein-DNA interactions.Covariation in frequencies of substitution, deletion, transposition, and recombination during eutherian evolutionGenome-wide sequence and functional analysis of early replicating DNA in normal human fibroblasts
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P50
description
hulumtues
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wetenschapper
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հետազոտող
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Terrence Furey
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Terrence S. Furey
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Terrence S. Furey
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Terrence S. Furey
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Terrence S. Furey
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Terrence Furey
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Terrence S. Furey
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Terrence S. Furey
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Terrence S. Furey
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Terrence S. Furey
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Terrence S Furey
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Terrence Furey
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Terrence S. Furey
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Terrence S. Furey
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Terrence S. Furey
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Terrence S. Furey
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P106
P1153
6602302257
P21
P31
P496
0000-0001-5546-9672