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Since the 1990s, it has also been possible to screen children from birth using objective, reliable, painless, and rapid methods [ 23].
Since 1992, it has been possible to screen DNA copy number amplifications in genome-wide coverage using comparative genomic hybridization (CGH) [ 10] and large amounts of DNA copy number data from different cancers have been published and collected [ 1, 11].
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If research can establish that is true, then it may be possible to screen infants and single out those at risk, so that parents can take suitable precautions.
It is possible to screen for genetic influence on behaviour by comparing the behaviour of different inbred strains raised in the same laboratory environment.
It is possible to screen asymptomatic individuals for various types of cancer, such as breast, cervical, prostate, colorectal, and skin cancers.
The good news here is that it might eventually be possible to screen breast cancers on a genetic level, using other kinds of tests—even blood tests to look for the biological traces of those genes.
While it might be possible to screen prospective executives for past successes in managing corporate growth or achieving favorable stock performance, how do you measure for something as apparently subjective as integrity?
The good news here is that it might eventually be possible to screen breast cancers on a genetic level, using other kinds of tests — even blood tests — to look for the biological traces of those genes.
By applying basic proteomics tools it is possible to screen large sample collections for fluorescent proteins of desired characteristics prior to gene cloning.
Using MASS, we show that it is possible to screen synthetic and natural product libraries in a high throughput and robust manner.
This study demonstrates that it is possible to screen potential antagonists of TNF-α using in vitro analysis systems in combination with the computer-aided modeling method.
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