Initial sequencing and analysis of the human genomeSwaposins: circular permutations within genes encoding saposin homologues8.2% of the Human genome is constrained: variation in rates of turnover across functional element classes in the human lineageLineage-specific biology revealed by a finished genome assembly of the mouseHigh levels of RNA-editing site conservation amongst 15 laboratory mouse strainsTwo Antarctic penguin genomes reveal insights into their evolutionary history and molecular changes related to the Antarctic environment.The western painted turtle genome, a model for the evolution of extreme physiological adaptations in a slowly evolving lineage.What fraction of the human genome is functional?The African coelacanth genome provides insights into tetrapod evolutionThe bonobo genome compared with the chimpanzee and human genomesInsights into hominid evolution from the gorilla genome sequenceThe genome of the green anole lizard and a comparative analysis with birds and mammalsComparative and demographic analysis of orang-utan genomesThe genome of a songbirdEvolution of genes and genomes on the Drosophila phylogenyGenome analysis of the platypus reveals unique signatures of evolutionGenome of the marsupial Monodelphis domestica reveals innovation in non-coding sequencesGenome sequence, comparative analysis and haplotype structure of the domestic dogSequence 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 genomeEvc2 is a positive modulator of Hedgehog signalling that interacts with Evc at the cilia membrane and is also found in the nucleusStromal cell-derived receptor 2 and cytochrome b561 are functional ferric reductasesA code for RanGDP binding in ankyrin repeats defines a nuclear import pathwayMonoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformationsThe obesity-associated FTO gene encodes a 2-oxoglutarate-dependent nucleic acid demethylaseTRAM, LAG1 and CLN8: members of a novel family of lipid-sensing domains?Identification of the MMS22L-TONSL complex that promotes homologous recombinationCoordination of structure-specific nucleases by human SLX4/BTBD12 is required for DNA repairEYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosaUIF, a New mRNA export adaptor that works together with REF/ALY, requires FACT for recruitment to mRNASMART: a web-based tool for the study of genetically mobile domains.Proteins of the endoplasmic-reticulum-associated degradation pathway: domain detection and function predictionMutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan.Functional impact of global rare copy number variation in autism spectrum disordersSMART, a simple modular architecture research tool: identification of signaling domainsThe protein composition of mitotic chromosomes determined using multiclassifier combinatorial proteomicsDefensins and the convergent evolution of platypus and reptile venom genesMutations in TOPORS cause autosomal dominant retinitis pigmentosa with perivascular retinal pigment epithelium atrophyA genetic variation map for chicken with 2.8 million single-nucleotide polymorphisms
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P50
description
British computational geneticist
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bioinformaticus
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英國計算遺傳學家
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name
Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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label
Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Paul Ponting
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Ponting CP
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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Chris Ponting
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