The discovery of human genetic variations and their use as disease markers: past, present and future.
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Characterization of complex chromosomal rearrangements by targeted capture and next-generation sequencingPairomics, the omics way to mate choiceGenotyping-by-sequencing (GBS): a novel, efficient and cost-effective genotyping method for cattle using next-generation sequencingFunctional expression of human adenine nucleotide translocase 4 in Saccharomyces cerevisiaeCD6 and syntaxin binding protein 6 variants and response to tumor necrosis factor alpha inhibitors in Danish patients with rheumatoid arthritisDevelopment of strategies for SNP detection in RNA-seq data: application to lymphoblastoid cell lines and evaluation using 1000 Genomes dataAn evaluation of copy number variation detection tools for cancer using whole exome sequencing data.Evaluating Phenotypic Data Elements for Genetics and Epidemiological Research: Experiences from the eMERGE and PhenX Network Projects.Genetics of age-related macular degeneration: current concepts, future directions.Personalised medicine in Canada: a survey of adoption and practice in oncology, cardiology and family medicineA chromosome 19 locus positively influences the number of retrieved oocytes during stimulated cycles in Brazilian womenPersonalized medicine in cardiovascular diseases.Androgen receptor polyglutamine repeat number: models of selection and disease susceptibility.Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error.Personalized medicine - the promised land: are we there yet?DNA methylation-based variation between human populations.Genome-wide association studies identify new targets in cardiovascular disease.Lane-by-lane sequencing using Illumina's Genome Analyzer II.Single Nucleotide Polymorphism Genotyping in Single-Molecule Electronic Circuits.Exploring the implications of INDELs in neuropsychiatric genetics: challenges and perspectives.Role of Genetics and Epigenetics in the Pathogenesis of Alzheimer's Disease and Frontotemporal Dementia.Noise cancellation using total variation for copy number variation detection
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P2860
The discovery of human genetic variations and their use as disease markers: past, present and future.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 20 May 2010
@en
vedecký článok
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vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
@cs
name
The discovery of human genetic ...... ers: past, present and future.
@en
The discovery of human genetic ...... ers: past, present and future.
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type
label
The discovery of human genetic ...... ers: past, present and future.
@en
The discovery of human genetic ...... ers: past, present and future.
@nl
prefLabel
The discovery of human genetic ...... ers: past, present and future.
@en
The discovery of human genetic ...... ers: past, present and future.
@nl
P2093
P2860
P356
P1476
The discovery of human genetic ...... kers: past, present and future
@en
P2093
Chee Seng Ku
En Yun Loy
Kee Seng Chia
Yudi Pawitan
P2860
P2888
P304
P356
10.1038/JHG.2010.55
P50
P577
2010-05-20T00:00:00Z