A high-quality human reference panel reveals the complexity and distribution of genomic structural variants.
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Human Y chromosome copy number variation in the next generation sequencing era and beyond.Negative selection in humans and fruit flies involves synergistic epistasis.Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome.Genotyping inversions and tandem duplications.The Necessity of Diploid Genome Sequencing to Unravel the Genetic Component of Complex Phenotypes.Mapping and phasing of structural variation in patient genomes using nanopore sequencing.Genomic predictions combining SNP markers and copy number variations in Nellore cattle.De novo human genome assemblies reveal spectrum of alternative haplotypes in diverse populations
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A high-quality human reference panel reveals the complexity and distribution of genomic structural variants.
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 06 October 2016
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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
A high-quality human reference ...... f genomic structural variants.
@en
A high-quality human reference ...... f genomic structural variants.
@nl
type
label
A high-quality human reference ...... f genomic structural variants.
@en
A high-quality human reference ...... f genomic structural variants.
@nl
prefLabel
A high-quality human reference ...... f genomic structural variants.
@en
A high-quality human reference ...... f genomic structural variants.
@nl
P2093
P2860
P50
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P1476
A high-quality human reference ...... f genomic structural variants.
@en
P2093
Abdel Abdellaoui
Alexander Schönhuth
Bradley P Coe
Djie Tjwan Thung
Eric-Wubbo Lameijer
Evan E Eichler
Fereydoun Hormozdiari
Freerk van Dijk
Genome of the Netherlands Consortium
Ivo Renkens
P2860
P2888
P356
10.1038/NCOMMS12989
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P577
2016-10-06T00:00:00Z