High resolution detection of genomic copy number abnormalities in a single cell is relevant to preimplantation genetic diagnosis and potentially to noninvasive prenatal diagnosis. Our objective is to develop a reliable array comparative genomic hybridization (CGH) platform to detect genomic imbalances as small as ~1Mb ina single cell.
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 06 April 2012.
All research outputs
#28,587,667
of 34,343,841 outputs
Outputs from Prenatal Diagnosis
#2,732
of 3,159 outputs
Outputs of similar age
#258,237
of 303,369 outputs
Outputs of similar age from Prenatal Diagnosis
#7
of 8 outputs
Altmetric has tracked 34,343,841 research outputs across all sources so far. This one is in the 9th percentile – i.e., 9% of other outputs scored the same or lower than it.
So far Altmetric has tracked 3,159 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 7.2. This one is in the 6th percentile – i.e., 6% of its peers scored the same or lower than it.
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We're also able to compare this research output to 8 others from the same source and published within six weeks on either side of this one.
