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Future medical applications of single-cell sequencing in cancer

Overview of attention for article published in Genome Medicine, May 2011
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About this Attention Score

  • Good Attention Score compared to outputs of the same age (66th percentile)

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343 Mendeley
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Title
Future medical applications of single-cell sequencing in cancer
Published in
Genome Medicine, May 2011
DOI 10.1186/gm247
Pubmed ID
Authors

Nicholas Navin, James Hicks

Abstract

Advances in whole genome amplification and next-generation sequencing methods have enabled genomic analyses of single cells, and these techniques are now beginning to be used to detect genomic lesions in individual cancer cells. Previous approaches have been unable to resolve genomic differences in complex mixtures of cells, such as heterogeneous tumors, despite the importance of characterizing such tumors for cancer treatment. Sequencing of single cells is likely to improve several aspects of medicine, including the early detection of rare tumor cells, monitoring of circulating tumor cells (CTCs), measuring intratumor heterogeneity, and guiding chemotherapy. In this review we discuss the challenges and technical aspects of single-cell sequencing, with a strong focus on genomic copy number, and discuss how this information can be used to diagnose and treat cancer patients.

X Demographics

X Demographics

The data shown below were collected from the profiles of 5 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 343 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 7 2%
Germany 3 <1%
United Kingdom 3 <1%
Netherlands 2 <1%
Belgium 2 <1%
Norway 1 <1%
Italy 1 <1%
Finland 1 <1%
Korea, Republic of 1 <1%
Other 8 2%
Unknown 314 92%

Demographic breakdown

Readers by professional status Count As %
Researcher 89 26%
Student > Ph. D. Student 76 22%
Student > Bachelor 31 9%
Student > Master 28 8%
Other 20 6%
Other 67 20%
Unknown 32 9%
Readers by discipline Count As %
Agricultural and Biological Sciences 146 43%
Biochemistry, Genetics and Molecular Biology 68 20%
Medicine and Dentistry 31 9%
Engineering 13 4%
Computer Science 10 3%
Other 31 9%
Unknown 44 13%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 4. 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 2013.
All research outputs
#7,713,861
of 25,373,627 outputs
Outputs from Genome Medicine
#1,186
of 1,585 outputs
Outputs of similar age
#41,428
of 122,204 outputs
Outputs of similar age from Genome Medicine
#13
of 16 outputs
Altmetric has tracked 25,373,627 research outputs across all sources so far. This one has received more attention than most of these and is in the 69th percentile.
So far Altmetric has tracked 1,585 research outputs from this source. They typically receive a lot more attention than average, with a mean Attention Score of 26.8. This one is in the 24th percentile – i.e., 24% 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 122,204 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 66% of its contemporaries.
We're also able to compare this research output to 16 others from the same source and published within six weeks on either side of this one. This one is in the 18th percentile – i.e., 18% of its contemporaries scored the same or lower than it.