OT: Problems with Nimblegen scans?
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@jdelasherasedacuk-1189
Last seen 9.3 years ago
United Kingdom
Hi list, this is not strictly BioC, but I know there is quite a few people here using Nimblegen arrays. Has anybody else experienced problems with their scans? In particular, I received data that was scanned with settings giving rise to a significantly larger amount of saturated features than expected/wanted. We had done an experiment comprising 4 hybs, in triplicate (12 chips). The first batch was very good (well, except from a duff hyb... which they didn't tell me, and only when I started enquiring -my data looked weird- they acknowledged the problem and re-hybed it). But the past month we did the other two sets, and their scans are too strong. Anybody else? Jose -- Dr. Jose I. de las Heras Email: J.delasHeras at ed.ac.uk The Wellcome Trust Centre for Cell Biology Phone: +44 (0)131 6513374 Institute for Cell & Molecular Biology Fax: +44 (0)131 6507360 Swann Building, Mayfield Road University of Edinburgh Edinburgh EH9 3JR UK
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@alicia-oshlack-2241
Last seen 10.2 years ago
Hi Jose, We experienced a similar thing with our custom Nimblegen arrays. We asked them to rescan the arrays again at a lower setting which improved things a bit but we still had some saturated probes. Cheers, Alicia Alicia Oshlack, PhD Division of Bioinformatics Walter and Eliza Hall Institute > Message: 15 > Date: Wed, 27 Jun 2007 01:51:18 +0100 > From: J.delasHeras at ed.ac.uk > Subject: [BioC] OT: Problems with Nimblegen scans? > To: bioconductor at stat.math.ethz.ch > Message-ID: <20070627015118.97eaqyxvk0ggo808 at www.staffmail.ed.ac.uk> > Content-Type: text/plain; charset=ISO-8859-1; DelSp="Yes"; > format="flowed" > > > Hi list, > > this is not strictly BioC, but I know there is quite a few people here > using Nimblegen arrays. > Has anybody else experienced problems with their scans? In particular, > I received data that was scanned with settings giving rise to a > significantly larger amount of saturated features than expected/wanted. > We had done an experiment comprising 4 hybs, in triplicate (12 chips). > The first batch was very good (well, except from a duff hyb... which > they didn't tell me, and only when I started enquiring -my data looked > weird- they acknowledged the problem and re-hybed it). But the past > month we did the other two sets, and their scans are too strong. > > Anybody else? > > Jose > > -- > Dr. Jose I. de las Heras Email: > J.delasHeras at ed.ac.uk > The Wellcome Trust Centre for Cell Biology Phone: +44 (0)131 6513374 > Institute for Cell & Molecular Biology Fax: +44 (0)131 6507360 > Swann Building, Mayfield Road > University of Edinburgh > Edinburgh EH9 3JR > UK > >
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Quoting Alicia Oshlack <oshlack at="" wehi.edu.au="">: > Hi Jose, > > We experienced a similar thing with our custom Nimblegen arrays. We > asked them to rescan the arrays again at a lower setting which improved > things a bit but we still had some saturated probes. > > Cheers, > Alicia That's great, Alicia. At least they re-scanned yours! Right now they're refusing to re-do mine [1]... what's most irritating is that they simply claim all my arrays were scanned in the same way and look they same... when I have the scatterplots right in front of me showing that they don't. I did send those to them... Not impressed with their service. And not the first incident either. And judging from my personal email (offlist), we're not the only ones experiencing problems. Jose [1] but there's no way we're accepting this. -- Dr. Jose I. de las Heras Email: J.delasHeras at ed.ac.uk The Wellcome Trust Centre for Cell Biology Phone: +44 (0)131 6513374 Institute for Cell & Molecular Biology Fax: +44 (0)131 6507360 Swann Building, Mayfield Road University of Edinburgh Edinburgh EH9 3JR UK
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