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Genotyping

Overview of attention for book
Cover of 'Genotyping'

Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 Genetic Fingerprinting Using Microsatellite Markers in a Multiplex PCR Reaction: A Compilation of Methodological Approaches from Primer Design to Detection Systems
  3. Altmetric Badge
    Chapter 2 Genotyping DNA Variants with High-Resolution Melting Analysis
  4. Altmetric Badge
    Chapter 3 High-Throughput Genotyping with TaqMan Allelic Discrimination and Allele-Specific Genotyping Assays
  5. Altmetric Badge
    Chapter 4 In Situ Single-Molecule RNA Genotyping Using Padlock Probes and Rolling Circle Amplification
  6. Altmetric Badge
    Chapter 5 The MassARRAY® System for Targeted SNP Genotyping
  7. Altmetric Badge
    Chapter 6 Genotyping
  8. Altmetric Badge
    Chapter 7 Genotyping
  9. Altmetric Badge
    Chapter 8 Analysis of Copy Number Variation Using the Paralogue Ratio Test (PRT)
  10. Altmetric Badge
    Chapter 9 Genotyping Multiallelic Copy Number Variation with Multiplex Ligation-Dependent Probe Amplification (MLPA)
  11. Altmetric Badge
    Chapter 10 Analysis of Multiallelic CNVs by Emulsion Haplotype Fusion PCR
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    Chapter 11 Quantitative DNA Analysis Using Droplet Digital PCR
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    Chapter 12 Full-Length Mitochondrial-DNA Sequencing on the PacBio RSII
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    Chapter 13 Targeted Locus Amplification and Next-Generation Sequencing
  15. Altmetric Badge
    Chapter 14 Genotyping
  16. Altmetric Badge
    Chapter 15 Rapid SNP Detection and Genotyping of Bacterial Pathogens by Pyrosequencing
  17. Altmetric Badge
    Chapter 16 Methods for Genotyping-by-Sequencing
  18. Altmetric Badge
    Chapter 17 Describing Sequence Variants Using HGVS Nomenclature
Attention for Chapter 7: Genotyping
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Chapter title
Genotyping
Chapter number 7
Book title
Genotyping
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6442-0_7
Pubmed ID
Book ISBNs
978-1-4939-6440-6, 978-1-4939-6442-0
Authors

Lemmers, Richard J L F, Richard J. L. F. Lemmers, Lemmers, Richard J. L. F.

Abstract

The myopathy facioscapulohumeral muscular dystrophy type 1 (FSHD1) is caused by copy number variation of the D4Z4 macrosatellite repeat on chromosome 4. In unaffected individuals the number of 3.3 kb D4Z4 units varies between 8 and 100, whereas 1-10 units are seen in FSHD1 cases. A homologous and heterogenous D4Z4 array can be found on chromosome 10q, but contractions of this array are typically not associated with FSHD. Discriminating between the chromosome 4 and chromosome 10 D4Z4 arrays, as well as determining the array size, requires the use of pulsed-field gel electrophoresis, Southern blotting, and the isolation of high-quality DNA.

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X Demographics

The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 5 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 5 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 1 20%
Researcher 1 20%
Student > Doctoral Student 1 20%
Unknown 2 40%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 40%
Agricultural and Biological Sciences 1 20%
Unknown 2 40%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 21 November 2016.
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#18,482,034
of 22,901,818 outputs
Outputs from Methods in molecular biology
#7,927
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Outputs of similar age
#310,530
of 420,462 outputs
Outputs of similar age from Methods in molecular biology
#691
of 1,074 outputs
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