Genotyping whole-genome-amplified DNA from 3- to 25-year-old neonatal dried blood spot samples with reference to fresh genomic DNA.
about
Optimized DNA extraction from neonatal dried blood spots: application in methylome profilingHigh quality genome-wide genotyping from archived dried blood spots without DNA amplification.Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis.Genotyping performance assessment of whole genome amplified DNA with respect to multiplexing level of assay and its period of storageIsolation of human genomic DNA for genetic analysis from premature neonates: a comparison between newborn dried blood spots, whole blood and umbilical cord tissue.CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastomaMannose-Binding Lectin Gene, MBL2, Polymorphisms Do Not Increase Susceptibility to Invasive Meningococcal Disease in a Population of Danish ChildrenEvaluation of sex-specific gene expression in archived dried blood spots (DBS)Visual automated fluorescence electrophoresis provides simultaneous quality, quantity, and molecular weight spectra for genomic DNA from archived neonatal blood spotsMethylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age at onset of schizophrenia: no consistent evidence for an association in the Nordic populationHigh quality methylome-wide investigations through next-generation sequencing of DNA from a single archived dry blood spot.Mannose-binding lectin gene, MBL2, polymorphisms are not associated with susceptibility to invasive pneumococcal disease in children.UGT1A1*28 polymorphism and acute lymphoblastic leukemia in children: a Danish case-control study.A comparative analysis of the governance and use of residual dried blood spots from state newborn screening programs and neonatal biobanks.DNA Methylation Analysis from Blood Spots: Increasing Yield and Quality for Genome-Wide and Locus-Specific Methylation Analysis.Research use of leftover newborn bloodspots: attitudes of Canadian geneticists regarding storage and informed consent requirements.The Prevalence of Mutations inKCNQ1, KCNH2,andSCN5Ain an Unselected National Cohort of Young Sudden Unexplained Death Cases
P2860
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P2860
Genotyping whole-genome-amplified DNA from 3- to 25-year-old neonatal dried blood spot samples with reference to fresh genomic DNA.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh
2009年學術文章
@zh-hant
name
Genotyping whole-genome-amplif ...... eference to fresh genomic DNA.
@en
Genotyping whole-genome-amplif ...... eference to fresh genomic DNA.
@nl
type
label
Genotyping whole-genome-amplif ...... eference to fresh genomic DNA.
@en
Genotyping whole-genome-amplif ...... eference to fresh genomic DNA.
@nl
prefLabel
Genotyping whole-genome-amplif ...... eference to fresh genomic DNA.
@en
Genotyping whole-genome-amplif ...... eference to fresh genomic DNA.
@nl
P2093
P356
P1433
P1476
Genotyping whole-genome-amplif ...... eference to fresh genomic DNA.
@en
P2093
Bent Norgaard-Pedersen
David Michael Hougaard
Poul Thorsen
P304
P356
10.1002/ELPS.200800655
P577
2009-07-01T00:00:00Z