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A project has recently been started to sequence the complete melon genome following a whole-genome shotgun strategy, which makes use of massive sequencing data.
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Cancer centers, for instance, are starting to sequence numerous genes in patients' tumors to help select the most effective drugs.
But there are few orthobunyavirus sequences available with which to compare the new virus, so scientists are starting to sequence more members of the family.
Since then, a lot of activities have been started to study summability, sequence spaces and related topics on 2-normed spaces [30 33].
Plummeting sequence prices are starting to make individual personal genome sequencing a diagnostic reality.
"What's exciting is that we're starting to see how genome sequence expresses itself through the epigenome," said Harvard geneticist Steven McCarroll, who wasn't involved in the studies.
In parallel, companies are starting to provide whole genome sequencing services, with the aim of understanding the individual's susceptibility for diseases, including different cancers.
The price of determining the DNA blueprint of a person is tumbling and sequencing is starting to be used for medical diagnosis, not just for basic research.
The result is that the ability to determine DNA sequences is starting to outrun the ability of researchers to store, transmit and especially to analyze the data.
The economics of using even higher density arrays platform vs. low coverage whole-genome sequencing is starting to tip.
Sequencing also is starting to help doctors decide who should take drugs to prevent diseases, as is happening with heart disease.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com