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Genetic Variation

Overview of attention for book
Cover of 'Genetic Variation'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Genetic Variation Analysis for Biomedical Researchers: A Primer
  3. Altmetric Badge
    Chapter 2 Exploring the Landscape of the Genome
  4. Altmetric Badge
    Chapter 3 Asking Complex Questions of the Genome Without Programming
  5. Altmetric Badge
    Chapter 4 Laboratory Methods for the Detection of Chromosomal Abnormalities
  6. Altmetric Badge
    Chapter 5 Cancer Genome Analysis Informatics
  7. Altmetric Badge
    Chapter 6 Copy Number Variations in the Human Genome and Strategies for Analysis
  8. Altmetric Badge
    Chapter 7 A Short Primer on the Functional Analysis of Copy Number Variation for Biomedical Scientists
  9. Altmetric Badge
    Chapter 8 Computational Methods for the Analysis of Primate Mobile Elements
  10. Altmetric Badge
    Chapter 9 Laboratory Methods for the Analysis of Primate Mobile Elements
  11. Altmetric Badge
    Chapter 10 Practical Informatics Approaches to Microsatellite and Variable Number Tandem Repeat Analysis
  12. Altmetric Badge
    Chapter 11 Genetic Variation
  13. Altmetric Badge
    Chapter 12 Whole genome sequencing.
  14. Altmetric Badge
    Chapter 13 Detection of Mitochondrial DNA Variation in Human Cells
  15. Altmetric Badge
    Chapter 14 An Introduction to Mitochondrial Informatics
  16. Altmetric Badge
    Chapter 15 Web-Based Analysis of (Epi-) Genome Data Using EpiGRAPH and Galaxy
  17. Altmetric Badge
    Chapter 16 Short tandem repeats and genetic variation.
  18. Altmetric Badge
    Chapter 17 Bioinformatic Tools for Identifying Disease Gene and SNP Candidates
  19. Altmetric Badge
    Chapter 18 Analysis of the Impact of Genetic Variation on Human Gene Expression
  20. Altmetric Badge
    Chapter 19 Quality control for genome-wide association studies.
  21. Altmetric Badge
    Chapter 20 Gaining a Pathway Insight into Genetic Association Data
Attention for Chapter 12: Whole genome sequencing.
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About this Attention Score

  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (95th percentile)
  • High Attention Score compared to outputs of the same age and source (95th percentile)

Mentioned by

news
1 news outlet
blogs
3 blogs
twitter
2 X users

Citations

dimensions_citation
15 Dimensions

Readers on

mendeley
516 Mendeley
citeulike
7 CiteULike
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Chapter title
Whole genome sequencing.
Chapter number 12
Book title
Genetic Variation
Published in
Methods in molecular biology, March 2010
DOI 10.1007/978-1-60327-367-1_12
Pubmed ID
Book ISBNs
978-1-60327-366-4, 978-1-60327-367-1
Authors

Ng PC, Kirkness EF, Pauline C. Ng, Ewen F. Kirkness, Ng, Pauline C., Kirkness, Ewen F.

Abstract

Whole genome sequencing provides the most comprehensive collection of an individual's genetic variation. With the falling costs of sequencing technology, we envision paradigm shift from microarray-based genotyping studies to whole genome sequencing. We review methodologies for whole genome sequencing. There are two approaches for assembling short shotgun sequence reads into longer contiguous genomic sequences. In the de novo assembly approach, sequence reads are compared to each other, and then overlapped to build longer contiguous sequences. The reference-based assembly approach involves mapping each read to a reference genome sequence. We discuss methods for identifying genetic variation (single nucleotide polymorphisms, small indels, and copy number variants) and building haplotypes from genome assemblies, and discuss potential pitfalls. We expect methodologies to evolve rapidly as sequencing technologies improve and more human genomes are sequenced.

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X Demographics

The data shown below were collected from the profiles of 2 X users 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 516 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 4 <1%
United Kingdom 3 <1%
Switzerland 1 <1%
Brazil 1 <1%
Nigeria 1 <1%
Nepal 1 <1%
Russia 1 <1%
China 1 <1%
Unknown 503 97%

Demographic breakdown

Readers by professional status Count As %
Student > Master 82 16%
Student > Bachelor 81 16%
Student > Ph. D. Student 65 13%
Researcher 42 8%
Other 16 3%
Other 56 11%
Unknown 174 34%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 139 27%
Agricultural and Biological Sciences 90 17%
Medicine and Dentistry 29 6%
Immunology and Microbiology 16 3%
Computer Science 10 2%
Other 48 9%
Unknown 184 36%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 26. 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 18 December 2020.
All research outputs
#1,243,670
of 22,661,413 outputs
Outputs from Methods in molecular biology
#144
of 13,020 outputs
Outputs of similar age
#4,202
of 94,157 outputs
Outputs of similar age from Methods in molecular biology
#1
of 20 outputs
Altmetric has tracked 22,661,413 research outputs across all sources so far. Compared to these this one has done particularly well and is in the 94th percentile: it's in the top 10% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 13,020 research outputs from this source. They receive a mean Attention Score of 3.3. This one has done particularly well, scoring higher than 98% of its peers.
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We're also able to compare this research output to 20 others from the same source and published within six weeks on either side of this one. This one has done particularly well, scoring higher than 95% of its contemporaries.