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Martin Kennedy: BIOT: ABI Genotyping | ||||||||||||||||
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To: Multiple recipients of list HUM-MOLGEN <HUM-MOLGEN@NIC.SURFNET.NL> Subject: BIOT: ABI Genotyping From: Martin Kennedy <MKENNEDY@chmeds.ac.nz> Date: Mon, 18 Sep 1995 10:36:16 +1200 Date sent: 18-SEP-1995 10:34:57 This message contains 2 posts responding to a question about the use of ABI machines for genotyping: 8< ======================= cut here ======================= >8 X-Sender: preston@pop.pitt.edu From: Robert Preston <rapr@MED.PITT.EDU> Subject: Re: BIOT, ANNO >I would like to know if anyone has tried the ABI setup (either automated >sequencer apparatus or the newer capillary format) for genotyping using >fluorescent primers. The demos look great and the capillary format is >supposed to cost 1/2 of what the ABI 373 costs. >Any info appreciated. >Thanks >Agnes We are now doing 3 runs per day on the 373A: two four-hour runs for genotyping with fluorescent primers (in one case, 36 lanes/gel with up to 4 loci per lane; in the other case, 24 lanes per gel with six loci per lane. The third run is an overnight 14 hour sequencing run. The machine works so well (and reliably) that we're trying to get another one. The capillary format machine is not field-proven, and is likely, in my opinion, to have much slower throughput than the flat-gel-based technology. I did the genotyping for mapping the Crouzon (FGFR2) locus using the 373, and it looks like we've bagged another gene since then. For genotyping, I'd take the 373 over the capillary thing any day. Robert A. Preston Pittsburgh, PA rapr@med.pitt.edu 8< ======================= cut here ======================= >8 X-Sender: gvcamp@hgins.uia.ac.be From: "Guy.VanCamp" <gvcamp@UIA.UA.AC.BE> answer to question: ABI for genotyping? Yes, I have experience with it. I have a paper in press that will be published in November in Human Molecular Genetics that describing the localization of a gene for hereditary deafness using a fluorescent, automated genome search on an ABI machine. We have developped software for automated data collection. A paper describing this is in preparation, and the software will be freely available in the future. I am prepared to give additional information if needed. Guy Van Camp, PhD Dept of Medical Genetics University of Antwerp 8< ======================= cut here ======================= >8 Cheers, Martin Kennedy/Arthur Bergen BIOT Topic Editors, HUM-MOLGEN
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