Mobile elements create structural variation: analysis of a complete human genome.
about
Human genetics and genomics a decade after the release of the draft sequence of the human genomeTopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusionsThe impact of retrotransposons on human genome evolutionNext-generation VariationHunter: combinatorial algorithms for transposon insertion discoveryA map of human genome variation from population-scale sequencingAlu expression in human cell lines and their retrotranspositional potentialMobile elements reveal small population size in the ancient ancestors of Homo sapiensNucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint libraryTransposable element detection from whole genome sequence dataThe Fine LINE: Methylation Drawing the Cancer LandscapeHuman transposon tectonicsGenomic relationship between SINE retrotransposons, Pol III-Pol II transcription, and chromatin organization: the journey from junk to jewelHuman molecular cytogenetics: From cells to nucleotidesExpressing genes do not forget their LINEs: transposable elements and gene expressionStructural Variation of Alu Element and Human DiseaseActivation of individual L1 retrotransposon instances is restricted to cell-type dependent permissive lociU6 snRNA Pseudogenes: Markers of Retrotransposition Dynamics in MammalsLINEs and SINEs of primate evolutionLINE-1 elements in structural variation and diseaseAnalysis of western lowland gorilla (Gorilla gorilla gorilla) specific Alu repeatsAlu mobile elements: from junk DNA to genomic gemsTransposable elements re-wire and fine-tune the transcriptomeEvolution of HLA-DRB genesLINEs, SINEs and other retroelements: do birds of a feather flock together?LINE-1 retrotransposition activity in human genomesWhole-genome resequencing allows detection of many rare LINE-1 insertion alleles in humansDiamonds and rust: how transposable elements influence mammalian genomes. Conference on Mobile Elements in Mammalian GenomesHigh-throughput sequencing reveals extensive variation in human-specific L1 content in individual human genomesActive human retrotransposons: variation and diseaseNatural mutagenesis of human genomes by endogenous retrotransposonsSomatic retrotransposition alters the genetic landscape of the human brainGenome sequencing of mouse induced pluripotent stem cells reveals retroelement stability and infrequent DNA rearrangement during reprogramming.Genome-wide mapping and assembly of structural variant breakpoints in the mouse genomeBTECH: a platform to integrate genomic, transcriptomic and epigenomic alterations in brain tumorsMobster: accurate detection of mobile element insertions in next generation sequencing data.The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository.DNA is structured as a linear "jigsaw puzzle" in the genomes of Arabidopsis, rice, and budding yeast.Insertion and deletion polymorphisms of the ancient AluS family in the human genome.Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features.Mobile element scanning (ME-Scan) by targeted high-throughput sequencing.
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Mobile elements create structural variation: analysis of a complete human genome.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 13 May 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Mobile elements create structural variation: analysis of a complete human genome.
@en
Mobile elements create structural variation: analysis of a complete human genome.
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type
label
Mobile elements create structural variation: analysis of a complete human genome.
@en
Mobile elements create structural variation: analysis of a complete human genome.
@nl
prefLabel
Mobile elements create structural variation: analysis of a complete human genome.
@en
Mobile elements create structural variation: analysis of a complete human genome.
@nl
P2093
P2860
P50
P356
P1433
P1476
Mobile elements create structural variation: analysis of a complete human genome
@en
P2093
Chad D Huff
Ewen F Kirkness
Lynn B Jorde
Mark A Batzer
Qiong Zhou
Samuel Levy
Shurjo K Sen
Yuhua Zhang
P2860
P304
P356
10.1101/GR.091827.109
P577
2009-05-13T00:00:00Z