I agree with genomeseeker - if the raw wells are low, this indicates a problem with the final enriched bead count going into the sequencing reaction.
If your read length distribution is strange, consider changing your cpb going into emPCR. This may be an artifact of mixed signals.
Both these problems could be linked - if an improper count was found after enrichment, enrichment % would be miscalculated.
Announcement
Collapse
No announcement yet.
X
-
If your raw wells are lower than expected check these things:
- equipment used for bead counting after enrichment; new settings required for Ti's smaller beads.
- enrichment procedure; maybe you're carrying over a large amount null beads to your sequencing run.
Leave a comment:
-
Originally posted by SeqWhiskey View PostWe just got the new emPCR kits with the mysterious "additive", so hopefully this helps. It is supposed to improve bead quality and we can now start using beads with up to 20% enrichment, much different than the previous 8% recommendation.... When I talk to our Roche tech I'll let you know if we find anything useful.
Best, Matt
D
Leave a comment:
-
We just got the new emPCR kits with the mysterious "additive", so hopefully this helps. It is supposed to improve bead quality and we can now start using beads with up to 20% enrichment, much different than the previous 8% recommendation.... When I talk to our Roche tech I'll let you know if we find anything useful.
Best, Matt
Leave a comment:
-
We're having the same problem. Raw wells are lower by an order of magnitude than what they should be, read length is much lower than it should be it just tapers off, very few quality reads. Our FLX runs have been excellent though and we just ran an FLX after the most recent Ti failure... We're contacting our rep, tech support and everyone else we can get ahold of but... so far Ti has not delivered. at all.
Leave a comment:
-
Have you just started experiencing these problems? Are you having problems enriching beads as well? What percentage of raw wells are you seeing? Example, how many beads are you loading and how many are registering as raw wells?
I would talk with your Roche/454 rep and see if they have any information.
Originally posted by pr0t3us View PostHi to everybody,
we have a 454-Titanium. We made some runs, but we have never obtained good results.
With 454-GS-FLX, we have never had problems; major of runs was like expected. With Titanium we obtain poor runs (less reads than expected, strange read length distribution, less raw weels then expected) .
Has someone the same problems ?
Leave a comment:
-
Titanium Runs
Hi to everybody,
we have a 454-Titanium. We made some runs, but we have never obtained good results.
With 454-GS-FLX, we have never had problems; major of runs was like expected. With Titanium we obtain poor runs (less reads than expected, strange read length distribution, less raw weels then expected) .
Has someone the same problems ?Tags: None
Latest Articles
Collapse
-
by seqadmin
The recent pandemic caused worldwide health, economic, and social disruptions with its reverberations still felt today. A key takeaway from this event is the need for accurate and accessible tools for detecting and tracking infectious diseases. Timely identification is essential for early intervention, managing outbreaks, and preventing their spread. This article reviews several valuable tools employed in the detection and surveillance of infectious diseases.
...-
Channel: Articles
11-27-2023, 01:15 PM -
-
by seqadmin
Microbiome research has led to the discovery of important connections to human and environmental health. Sequencing has become a core investigational tool in microbiome research, a subject that we covered during a recent webinar. Our expert speakers shared a number of advancements including improved experimental workflows, research involving transmission dynamics, and invaluable analysis resources. This article recaps their informative presentations, offering insights...-
Channel: Articles
11-09-2023, 07:02 AM -
ad_right_rmr
Collapse
News
Collapse
Topics | Statistics | Last Post | ||
---|---|---|---|---|
Started by seqadmin, Today, 02:24 PM
|
0 responses
11 views
0 likes
|
Last Post
by seqadmin
Today, 02:24 PM
|
||
Started by seqadmin, Today, 07:37 AM
|
0 responses
20 views
0 likes
|
Last Post
by seqadmin
Today, 07:37 AM
|
||
Started by seqadmin, Yesterday, 08:23 AM
|
0 responses
8 views
0 likes
|
Last Post
by seqadmin
Yesterday, 08:23 AM
|
||
Started by seqadmin, 12-01-2023, 09:55 AM
|
0 responses
23 views
0 likes
|
Last Post
by seqadmin
12-01-2023, 09:55 AM
|
Leave a comment: