Personalized copy number and segmental duplication maps using next-generation sequencing. - Wikidata - wikimedia - TriplyDB

Personalized copy number and segmental duplication maps using next-generation sequencing.

Personalized copy number and segmental duplication maps using next-generation sequencing.

http://www.wikidata.org/entity/Q33498358

about

Genome sequencing highlights the dynamic early history of dogs COPS: a sensitive and accurate tool for detecting somatic Copy Number Alterations using short-read sequence data from paired samples Between a chicken and a grape: estimating the number of human genes 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 Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives Genomic legacy of the African cheetah, Acinonyx jubatus A Draft Sequence of the Neandertal Genome Repetitive DNA and next-generation sequencing: computational challenges and solutions Insights into hominid evolution from the gorilla genome sequence Complete Khoisan and Bantu genomes from southern Africa.Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosa A high-coverage genome sequence from an archaic Denisovan individual Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery Diversity of human copy number variation and multicopy genes Using ERDS to infer copy-number variants in high-coverage genomes Mapping copy number variation by population-scale genome sequencing SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci Clinical implementation of comprehensive strategies to characterize cancer genomes: opportunities and challenges Advances in BAC-based physical mapping and map integration strategies in plants Computational and bioinformatics frameworks for next-generation whole exome and genome sequencing Detection of Genomic Structural Variants from Next-Generation Sequencing Data Complex and multi-allelic copy number variation in human disease High-throughput droplet digital PCR system for absolute quantitation of DNA copy number Detection of chromosomal alterations in the circulation of cancer patients with whole-genome sequencing CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing PeSV-Fisher: identification of somatic and non-somatic structural variants using next generation sequencing data Efficient In Silico Identification of a Common Insertion in the MAK Gene which Causes Retinitis Pigmentosa Chromosomal Rearrangements as Barriers to Genetic Homogenization between Archaic and Modern Humans Tracking the origins of Yakutian horses and the genetic basis for their fast adaptation to subarctic environments Tumour evolution inferred by single-cell sequencing A primer for disease gene prioritization using next-generation sequencing data The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration Next-generation genomics: an integrative approach Comparative analysis of copy number variation detection methods and database construction Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing

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P2860

Personalized copy number and segmental duplication maps using next-generation sequencing.

http://www.wikidata.org/entity/Q33498358

description

2009 nî lūn-bûn

@nan

2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

Personalized copy number and segmental duplication maps using next-generation sequencing.

@ast

Personalized copy number and segmental duplication maps using next-generation sequencing.

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type

label

Personalized copy number and segmental duplication maps using next-generation sequencing.

@ast

Personalized copy number and segmental duplication maps using next-generation sequencing.

@en

prefLabel

Personalized copy number and segmental duplication maps using next-generation sequencing.

@ast

Personalized copy number and segmental duplication maps using next-generation sequencing.

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Nature Genetics

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Personalized copy number and segmental duplication maps using next-generation sequencing

@en

P2093

Carl Baker

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Evan E Eichler

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Fereydoun Hormozdiari

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Gozde Aksay

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Maika Malig

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Onur Mutlu

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Richard A Gibbs

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S Cenk Sahinalp

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P2860

The diploid genome sequence of an Asian individual

Fine-scale structural variation of the human genome

Mapping and sequencing of structural variation from eight human genomes

The complete genome of an individual by massively parallel DNA sequencing

Accurate whole human genome sequencing using reversible terminator chemistry

Mapping short DNA sequencing reads and calling variants using mapping quality scores

Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing

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

Global variation in copy number in the human genome

NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

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1061-1067

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10.1038/NG.437

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10

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41

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Tomas Marques-Bonet

Jeffrey M. Kidd

Francesca Antonacci

Jacob O Kitzman

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2009-08-30T00:00:00Z

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26777785

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19718026

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2875196

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