High-throughput multiplex sequencing to discover copy number variants in Drosophila
about
A reduced representation approach to population genetic analyses and applications to human evolutionChromosomal structural variations during progression of a prostate epithelial cell line to a malignant metastatic state inactivate the NF2, NIPSNAP1, UGT2B17, and LPIN2 genesSingle-molecule sequencing of an individual human genome.Population genomic inferences from sparse high-throughput sequencing of two populations of Drosophila melanogasterSeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data.Combining target enrichment with barcode multiplexing for high throughput SNP discoveryStructural variation in the chicken genome identified by paired-end next-generation DNA sequencing of reduced representation libraries.Notch activation as a driver of osteogenic sarcoma.De novo characterization of Larix gmelinii (Rupr.) Rupr. transcriptome and analysis of its gene expression induced by jasmonatesIdentifying gene disruptions in novel balanced de novo constitutional translocations in childhood cancer patients by whole-genome sequencing.Copy number polymorphism in plant genomesCharacterizing natural variation using next-generation sequencing technologies.Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimensDetection of breed-specific copy number variations in domestic chicken genome.Identification and Quantification of Genomic Repeats and Sample Contamination in Assemblies of 454 Pyrosequencing Reads
P2860
Q28742975-3F506CF5-C40E-4FCF-BB10-AB1F096FB1E2Q30414829-3301576E-42FE-43DF-9E72-90A4BFD6E5F6Q30434015-26731395-7965-4AE2-8CB7-E088A27EB8FCQ30436703-D77AFD83-B6B0-4E26-AB47-2470B6EF970AQ31169803-954DAC4F-6A97-4C63-A9E9-2776A356503DQ33749069-6E6B47C4-03F2-4F64-9959-4355AA7017D1Q33811233-ACDB2287-5312-45CA-9901-9B51A1CEF0CFQ34157487-493835AF-0599-4B73-AC4F-CECBAF7201FBQ34938997-DFA33BE1-E9CD-40D1-807F-5D2476F9E16BQ35832773-DE083401-669A-4EB8-BD72-B17DB18474B7Q35981240-4F30AA5A-2D3F-4801-BCB2-75C615E287ADQ37607823-10E34B98-DE39-478F-A274-EBBC927FCA18Q38416233-7A655971-47BA-4FB0-8F27-7C7C6A2EDB64Q54176390-41CFE4E6-A4D6-4E29-AFF8-B413B67C1387Q57817195-79BCD917-3922-4FEA-AB4A-B06A1B2A9C2C
P2860
High-throughput multiplex sequencing to discover copy number variants in Drosophila
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 15 June 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
High-throughput multiplex sequencing to discover copy number variants in Drosophila
@en
High-throughput multiplex sequencing to discover copy number variants in Drosophila.
@nl
type
label
High-throughput multiplex sequencing to discover copy number variants in Drosophila
@en
High-throughput multiplex sequencing to discover copy number variants in Drosophila.
@nl
prefLabel
High-throughput multiplex sequencing to discover copy number variants in Drosophila
@en
High-throughput multiplex sequencing to discover copy number variants in Drosophila.
@nl
P2093
P2860
P1433
P1476
High-throughput multiplex sequencing to discover copy number variants in Drosophila
@en
P2093
P2860
P304
P356
10.1534/GENETICS.109.103218
P407
P50
P577
2009-06-15T00:00:00Z