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From Consultant to Consul


Potential subscribers to Celera’s database might deal with Lothar Krinke, the company’s newest cheerleader. The newly installed vice president of business development and strategic planning works with online information as well as discovery and M&A efforts.

Though Krinke studied molecular biology, his experience is in business. He worked at consulting firms McKinsey and A.T. Kearney, focusing on biopharmaceuticals and R&D. “Then I turned 39,” he says, “and I thought, ‘I’ve been doing consulting for 10 years. It’s time for me to go back into the field.’”

That field was decidedly small. Krinke selected just three companies he would work for. “Celera was on top,” he says, declining to name the other two.

Leaving consulting was no light decision. “I have totally committed my personal fortune and energy to this company,” Krinke says, declining to elaborate. “There is not an option for me for this to fail.”

What drew Krinke was Celera’s high risk, high reward model — and he doesn’t seem to have doubts about his leap into genomics. “Whatever we do is going to be big,” he says. “I am convinced that this company is going to be unbelievably successful.”

— Meredith Salisbury


The Scan

LINE-1 Linked to Premature Aging Conditions

Researchers report in Science Translational Medicine that the accumulation of LINE-1 RNA contributes to premature aging conditions and that symptoms can be improved by targeting them.

Team Presents Cattle Genotype-Tissue Expression Atlas

Using RNA sequences representing thousands of cattle samples, researchers looked at relationships between cattle genotype and tissue expression in Nature Genetics.

Researchers Map Recombination in Khoe-San Population

With whole-genome sequences for dozens of individuals from the Nama population, researchers saw in Genome Biology fine-scale recombination patterns that clustered outside of other populations.

Myotonic Dystrophy Repeat Detected in Family Genome Sequencing Analysis

While sequencing individuals from a multi-generation family, researchers identified a myotonic dystrophy type 2-related short tandem repeat in the European Journal of Human Genetics.