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omation mbers - Society for Laboratory Automation and Screening

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WP015<br />

Diane Johnson<br />

Pfizer Global Development <strong>and</strong> Research<br />

Material Management<br />

Eastern Point Road, Box 7031-10<br />

Groton, Connecticut 06340<br />

diane_l_johnson@groton.pfizer.com<br />

199<br />

Co-Author(s)<br />

Steve Brinkman, William Heineman,<br />

Craig Hines, Michele Kelly,<br />

Kim Matus<br />

Pfizer Global Research <strong>and</strong> Development Material Management Global Center of Emphasis:<br />

Global Liquid Operations at the Groton Kings Heights Technology Center<br />

Material Management global liquid operations focuses around a two Centers of Emphasis (CoE) model; one CoE<br />

in Europe (S<strong>and</strong>wich) <strong>and</strong> one CoE in the US (Kings Heights Technology Center, Groton Connecticut). The CoE<br />

storage <strong>and</strong> distribution model optimizes liquid compound h<strong>and</strong>ling access, speed, <strong>and</strong> efficiency by centralizing<br />

production functions. The Material Management-CoE model provides <strong>for</strong> redundant processing, storage <strong>and</strong><br />

distribution capability at two sites <strong>for</strong> all of Pfizer Global Research <strong>and</strong> Development. Vital to the success of the<br />

CoE concept <strong>and</strong> global ordering was the adoption a uni<strong>for</strong>m set of business rules <strong>and</strong> the deployment of a<br />

global ordering plat<strong>for</strong>m. Groton Material Management remains committed to providing high quality compound<br />

stewardship, storage, <strong>and</strong> processing together with corresponding data necessary to support Pfizer Global<br />

Research <strong>and</strong> Development needs.<br />

WP016<br />

Mike Jones<br />

Cambridge Antibody Technology Aut<strong>omation</strong><br />

Milstein Building, Granta Park<br />

Cambridge, Cambridgeshire CB1 6GH United Kingdom<br />

mike.jones@cambridgeantibody.com<br />

Automated DNA Sequencing: Quality Not Quantity<br />

Co-Author(s)<br />

Richard Stevens<br />

Kate Goode<br />

The DNA Chemistry facility at Cambridge Antibody Technology (CAT) is responsible <strong>for</strong> sequencing 20,000<br />

antibody fragments per month. The quality of the sequence data returned to the scientist is critical <strong>for</strong> identifying<br />

unique antibodies <strong>for</strong> further analysis. Good quality data means that the downstream process of analysing<br />

sequences is significantly reduced. Automated workstations have been set up to improve the efficiency <strong>and</strong><br />

quality of the results, <strong>and</strong> the pass rate <strong>for</strong> first time submitted sequences is 90% or greater. Automated systems<br />

provide reproducibility through the process, along with a greatly reduced error rate than would normally be seen<br />

if the process was done manually. Flexibility, diversity, <strong>and</strong> a short process time frame have dictated the use of a<br />

workstation approach rather than a large fully automated system, with the same machine used <strong>for</strong> different parts<br />

of the process. This means that if any piece of equipment is down then the process does not come to a st<strong>and</strong> still.<br />

Here we show how we have automated DNA sequencing in the laboratory with a Tecan Genesis workstation, a<br />

Tecan Miniprep <strong>and</strong> a Perkin Elmer Evolution P3 pipettor.<br />

POSTER ABSTRACTS

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