Mapping and sequencing of structural variation from eight human genomes - Wikidata - thesis-toulmin - TriplyDB

Mapping and sequencing of structural variation from eight human genomes

Mapping and sequencing of structural variation from eight human genomes

http://www.wikidata.org/entity/Q22122215

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Bacteria-human somatic cell lateral gene transfer is enriched in cancer samples Death and resurrection of the human IRGM gene Chromosome copy number variation and control in the ciliate Chilodonella uncinata COPS: a sensitive and accurate tool for detecting somatic Copy Number Alterations using short-read sequence data from paired samples Gene copy-number polymorphism caused by retrotransposition in humans Modernizing reference genome assemblies Towards a comprehensive structural variation map of an individual human genome Human genetics and genomics a decade after the release of the draft sequence of the human genome Evolutionary dynamics of copy number variation in pig genomes in the context of adaptation and domestication A high-resolution integrated map of copy number polymorphisms within and between breeds of the modern domesticated dog Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene The diploid genome sequence of an Asian individual Personal genome sequencing: current approaches and challenges Mechanisms of change in gene copy number Finding the missing heritability of complex diseases The human Major Histocompatibility Complex as a paradigm in genomics research Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery Diversity of human copy number variation and multicopy genes inGAP-sv: a novel scheme to identify and visualize structural variation from paired end mapping data Using ERDS to infer copy-number variants in high-coverage genomes Comprehensive long-span paired-end-tag mapping reveals characteristic patterns of structural variations in epithelial cancer genomes Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication Mapping copy number variation by population-scale genome sequencing Targeted capture and massively parallel sequencing of 12 human exomes Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls CNV and nervous system diseases--what's new?Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans Accurate whole human genome sequencing using reversible terminator chemistry Advances in translational bioinformatics: computational approaches for the hunting of disease genes Ultraconserved elements: analyses of dosage sensitivity, motifs and boundaries Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding The first Korean genome sequence and analysis: full genome sequencing for a socio-ethnic group Statistical aspects of discerning indel-type structural variation via DNA sequence alignment Copy number variation and schizophrenia Global distribution of genomic diversity underscores rich complex history of continental human populations Massively parallel sequencing: the next big thing in genetic medicine De novo assembly of human genomes with massively parallel short read sequencing Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes The UCSC Genome Browser Database: update 2009

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Mapping and sequencing of structural variation from eight human genomes

http://www.wikidata.org/entity/Q22122215

description

2008 nî lūn-bûn

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2008 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2008 թվականի մայիսին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

Mapping and sequencing of structural variation from eight human genomes

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Mapping and sequencing of structural variation from eight human genomes

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Mapping and sequencing of structural variation from eight human genomes

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Mapping and sequencing of structural variation from eight human genomes

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type

label

Mapping and sequencing of structural variation from eight human genomes

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Mapping and sequencing of structural variation from eight human genomes

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Mapping and sequencing of structural variation from eight human genomes

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Mapping and sequencing of structural variation from eight human genomes

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prefLabel

Mapping and sequencing of structural variation from eight human genomes

@ast

Mapping and sequencing of structural variation from eight human genomes

@en

Mapping and sequencing of structural variation from eight human genomes

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Mapping and sequencing of structural variation from eight human genomes

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Mapping and sequencing of structural variation from eight human genomes

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Adrianne Brand

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Brian Teague

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Daniel A Peiffer

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Gregory M Cooper

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Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

The diploid genome sequence of an individual human

Fine-scale structural variation of the human genome

Strong association of de novo copy number mutations with autism

Paired-end mapping reveals extensive structural variation in the human genome

Global variation in copy number in the human genome

End-sequence profiling: sequence-based analysis of aberrant genomes

A chromosome 8 gene-cluster polymorphism with low human beta-defensin 2 gene copy number predisposes to Crohn disease of the colon

A haplotype map of the human genome

Detection of large-scale variation in the human genome

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415421

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10.1038/NATURE06862

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7191

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453

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Jeffrey M. Kidd

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2008-05-01T00:00:00Z

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