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A new model calling procedure for Illumina BeadArray data

Overview of attention for article published in BMC Genomic Data, June 2016
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Title
A new model calling procedure for Illumina BeadArray data
Published in
BMC Genomic Data, June 2016
DOI 10.1186/s12863-016-0398-x
Pubmed ID
Authors

Gengxin Li

Abstract

Accurate genotype calling for high throughput Illumina data is an important step to extract more genetic information for a large scale genome wide association studies. Many popular calling algorithms use mixture models to infer genotypes of a large number of single nucleotide polymorphisms in a fast and efficient way. In practice, mixture models are mostly restricted to infer genotypes for common SNPs where their minor allele frequencies are quite large. However, it is still challenging to accurately genotype rare variants, especially for some rare variants where the boundaries of their genotypes are not clearly defined. To further improve the call accuracy and the quality of genotypes on rare variants, a new model calling procedure, named M-D, is proposed to infer genotypes for the Illumina BeadArray data. In this calling procedure, a Gaussian Mixture Model and a Dirichlet Process Gaussian Mixture Model are integrated to infer genotypes. Applications to Illumina data illustrate that this new approach can improve calling performance compared to other popular genotyping algorithms.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 11 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 11 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 45%
Student > Ph. D. Student 3 27%
Other 1 9%
Unknown 2 18%
Readers by discipline Count As %
Agricultural and Biological Sciences 6 55%
Computer Science 2 18%
Biochemistry, Genetics and Molecular Biology 1 9%
Unknown 2 18%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. 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 06 July 2016.
All research outputs
#16,722,190
of 25,374,917 outputs
Outputs from BMC Genomic Data
#604
of 1,204 outputs
Outputs of similar age
#227,919
of 368,661 outputs
Outputs of similar age from BMC Genomic Data
#18
of 47 outputs
Altmetric has tracked 25,374,917 research outputs across all sources so far. This one is in the 32nd percentile – i.e., 32% of other outputs scored the same or lower than it.
So far Altmetric has tracked 1,204 research outputs from this source. They receive a mean Attention Score of 4.3. This one is in the 45th percentile – i.e., 45% of its peers scored the same or lower than it.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 368,661 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 35th percentile – i.e., 35% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 47 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 51% of its contemporaries.