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7 Current white paper about the topic genetics

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Improved experimental setup for analysis of circadian rhythms using the nightshade

An improved Plant In Vivo Imaging protocol for circadian rhythms experiments using the NightShade

01-Mar-2018

An experimental setup that improves data quality, reduces luminescence variation between replicates and highly correlates with modelling predictions

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A novel solid-state ChIP platform in high throughput format – Chromatrap® 96 HT

04-May-2015

Epigenetics is increasingly a key focus of research groups in both industry and academia for answers to fundamental transcription regulation questions

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RealTime ready qPCR Assay Design and Configuration Portal Content

01-Jun-2011

The gene and transcript annotational content of the RealTime ready Configurator offers a combined view of three of the main gene annotation authorities. The positional information of the lab-tested RealTime ready assays regarding transcript or exon c

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High-Throughput Cardiac Gene Expression Analysis Using the Universal ProbeLibrary and the Novel LightCycler® 1536 Real-Time PCR System

25-Jan-2010

Although congenital heart malformations are the most common birth defects in humans, the underlying patho­mechanisms remain widely unknown. Through linkage analyzes and candidate-gene approaches, several gene mutations causing congenital heart defect

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Major Histocompatibility Complex Genotyping with Massively Parallel Pyrosequencing

04-Jan-2010

Macaques provide essential preclinical models for infectious disease, vaccine, biodefense, and transplantation research. Unfortunately, they also have the most complex MHC genetics of any primate species described to date, and existing methods for MH

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Array Capture-mediated Resequencing Leads to the Discovery of Four Novel Mutations in the Mouse

02-Dec-2009

By using array-based sequence capture and pyrosequencing to sequence an allelic series from the classically defined Kit locus (~200 kb) from each of five noncomplementing Kit mutants (one known allele and four unknown alleles), D'Ascenzo and co-worke

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Acquired Copy Number Alterations in Adult Acute Myeloid Leukemia Genomes

30-Nov-2009

To complement cytogenetic studies and to identify genes altered in AML genomes, Walter and co-workers performed a genome-wide copy number analysis with paired normal and tumor DNA obtained from 86 adult subjects with de novo AML using 1.85 million fe

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