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Thread | Thread Starter | Forum | Replies | Last Post |
Lots of false positives with SAMtools SNP discovery | mikael | Genomic Resequencing | 4 | 02-28-2011 07:38 AM |
Did Solid change their primer system? | SongLi | Bioinformatics | 1 | 12-20-2010 04:56 PM |
Going from biotinylated primer to unlabeled primer in emPCR | chunnan20451 | 454 Pyrosequencing | 0 | 09-01-2010 06:22 PM |
CPB correction with emPCR format change | 454User | 454 Pyrosequencing | 4 | 07-20-2010 10:49 AM |
Primer extension capture | tiayyba | Sample Prep / Library Generation | 3 | 03-28-2010 07:34 AM |
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#1 |
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Location: Colorado Join Date: Jul 2012
Posts: 20
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We just tried our first run with the new lot emPCR kits in which Roche has included a note that states the capture beads were changed and the amplification primer concentration was changed. This was supposed to increase uniformity in the emPCR amplification. These changes began with LOT# 93880860.
What we experienced: Increased number of short quality failures, basically cutting our passed filter wells in half. Nothing else seemed abnormal, aside from getting about 1,000,000 enriched beads rather than the 4-600k we usually get. Has anyone else tried these new lots and experienced anything like this? I am assuming they increased primer concentration.' Thanks! |
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#2 |
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Location: Australia Join Date: May 2009
Posts: 155
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The changes are described briefly in Tech bulletin 2012-007. It does say that the changes can increase the chance of amplifying short fragments, such as primer dimers. For the FLX these changes start with lot 93880220. I assume I'll get one of these lots with my next order.
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#3 |
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Location: Colorado Join Date: Jul 2012
Posts: 20
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Yes we read the tech bulletin and thought we should be okay as we use a Lonza flash gel system to purify amplicon of any primer dimers and short fragments. I suppose there could be some getting through but this seems more like an issue with the reagents, not my purification technique, we sequenced the day before this run using the old, unmodified lots and did not have nearly as many short quality failures. The histrogram indicates there were not short reads in the run using the new reagents as well.
Would like to hear experiences with these new reagents if uyou guys get them. |
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#4 |
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Location: Ohio Join Date: Dec 2010
Posts: 95
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Does anybody have any more info on these new reagents? How enrichment percentages compare, for example?
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#5 |
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Location: Colorado Join Date: Jul 2012
Posts: 20
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We just ran 2 more pools of amplicon last night for emPCR. Broke and enriched this morning, ended up with about 3x enriched beads that we usually get (up to 1.5 million enriched from our usual 500k).
Will let you know how sequencing turns out tomorrow. I would expect that we get a high number of short quality filter trims again. J |
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#6 | |
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Location: Colorado Join Date: Jul 2012
Posts: 20
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ANYONE ELSE?! Somebody has to be using these new lots |
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#7 |
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Location: Ohio Join Date: Dec 2010
Posts: 95
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Would you be able to provide cpb ratios and enrichment percentages comparing the old lots to the new? I know that would help me out!
I had to go up to 32 cpb to get 7.7% last week, (with the older lots) and now I have the new lots and I have no idea where to start.. |
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#8 |
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Location: Colorado Join Date: Jul 2012
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Right now I don't have time to post a lot of data, but I can tell you we are doing 1 cpb with new and old lots. Sequencing 400 bp amplicon, with 1/4 the amount of reccomended amp primer. We went from getting 400-600k enrichement consistenly for the last year to over 1 million on the last few runs with nothing changing except the lots.
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#9 |
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Location: Ohio Join Date: Dec 2010
Posts: 95
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Which kits are you using?
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#10 |
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Location: Colorado Join Date: Jul 2012
Posts: 20
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I'm using the rapid library Lib-A kit, on GS Junior. I know the concentrations changed similarly for FLX sequencing too, as this was included on the tech bulletin. See above post for the actual lot number.
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#11 |
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Location: Ohio Join Date: Dec 2010
Posts: 95
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So you've gone from ~10% enrichment to 20-30%. Interesting.
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#12 |
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Location: Colorado Join Date: Jul 2012
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#13 |
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Location: Ohio Join Date: Dec 2010
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I wonder if there are actually short fragments, or if it's one of the other parameters that is included in the short quality filter..I'm not familiar with the Jr, but this was a common problem with the FLX.
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#14 |
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Location: Colorado Join Date: Jul 2012
Posts: 20
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Actually had a decent run yesterday, given the huge enrichment. 90k reads, only 88k short quality. Maybe it was a fluke? Running another tonight, this will sway me one way or another.
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#15 |
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Location: Colorado Join Date: Jul 2012
Posts: 20
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I don't know whether to laugh or cry about this post. And yes, you certainly are a big dope.
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#16 |
Super Moderator
Location: US Join Date: Nov 2009
Posts: 437
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Posting garbage once is possibly funny, posting it more than once is spam.
Last edited by adaptivegenome; 07-18-2012 at 01:11 PM. Reason: typo |
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#17 |
--Site Admin--
Location: SF Bay Area, CA, USA Join Date: Oct 2007
Posts: 1,358
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Let's keep it relatively serious and professional, Dope. Thanks.
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#18 |
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Location: Manchester Join Date: Oct 2011
Posts: 14
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I enquired to Roche about just how the concentration of the primer in the emPCR kits had been changed and I have just had a response.
"The concentration of the primer in the kit was actually deceased (sic) by about 4 fold." |
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#19 |
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Location: Toronto Join Date: Mar 2011
Posts: 39
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so....
I am having one heck of a time with old emPCR kits. I am having an enrichment nightmare where I simply cannot get any freaking enriched beads out of this (extremely low %, regardless of CPB). I hope these new kits can do better for me but you guys aren't exactly giving me confidence. |
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#20 | |
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Location: Montana Join Date: Nov 2008
Posts: 21
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As for the increasing enrichments with the newer kits, we haven't really noticed this, however our enrichments are higher on plates that sit for a while after the final emulsion shake. We find that these "false" higher enrichments tend to sequence poorly. Same CPB, Same reagents, just the 1st cup sitting out longer while the second is being aliquoted = poorer sequence. As a result, we have gone to processing one LV cup at a time, putting them on the thermalcycler ASAP once aliquoted. Processing the cups this way is much more consistent, albeit more time consuming. |
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