By Julia Karow

As Illumina sequencers in particular, as well as the 454 platform, have become the workhorses for a variety of sequencing projects at the Broad Institute, its scientists have fine-tuned their sample-prep methods to keep the machines fed at all times.

At the Evolution of Next-Generation Sequencing conference in Providence last month, two members of the Broad's process development team shared some of the changes that have made sample prep faster, cheaper, and more high-throughput.

Get the full story with
GenomeWeb Premium

Only $95 for the
first 90 days*

A trial upgrade to GenomeWeb Premium gives you full site access, interest-based email alerts, access to archives, and more. Never miss another important industry story.

Try GenomeWeb Premium now.

Already a GenomeWeb Premium member? Login Now.
Or, See if your institution qualifies for premium access.

*Before your trial expires, we’ll put together a custom quote with your long-term premium options.

Not ready for premium?

Browse our free articles
You can still register for access to our free content.

In Genome Research this week: multiplex genotyping of germline and somatic short tandem repeats, graph-based regularization, and more.

A lack of funding may lead more than two dozen research facilities in Australia to shut down in three months.

Researchers report that paternally inherited genes are more likely to be expressed in mice.

National Institutes of Health Director Francis Collins appears before a House subcommittee to discuss his agency's budget request.