Has anyone automated any or all of the Illumina library prep steps on a robot? Beckman, Tecan, Hamilton? Any help will be appreciated. Thanks
Unconfigured Ad
Collapse
X
-
Same here
Looking for Library prep automation to increase throughput and eliminate variations caused by different users. In addition to the automation mentioned above from BIG_SNP, are there any other new instrumentation for full automation, say with thermal blocks?
Comment
-
-
Input is fragmented DNA (not cleaned up), output is adaptor ligated lib. ready for PCR.Originally posted by Michael L. Altshuler View PostSPRIworks Fragment Library System I and II are claimed to be the walk away automates for the library preparation (Beckman Genomics). I would like to know what they actually do, especially the start point (blood?) and endpoint (Adaptor Ligation???) for Illumina library
Comment
-
-
We are currently trying to automate as much of the set up as possible. We are using DNA fragmentase to fragment the DNA and think we can automate a number of the subsequent ligation and adapter annealing steps, although this involves manually placing plates onto PCR blocks. We are going to be using the ampure xp for the PCR clean up steps and dont envisage that being problematic. Finally we are using nimblegen sequence capture in solution and have a protocol for that but we have not run any samples yet. We are going to use a beckman Fx for the pre-PCR steps and a beckman Nx for the post-PCR steps and we are aiming to run a test batch of samples in the next 2 weeks once all our reagents arrive. I'd be happy to pass on details when we have an optimised pipeline.
Comment
-
-
Hi, I can confirm what James said above. The Sanger use a Biomek FX and a Biomek NX to automate their library prep for the Illumina. Beckman also have another site in the UK automating 96 library preps at a time on the Biomek FX with qPCR set up done on a Biomek 3000.
Comment
-
Latest Articles
Collapse
-
by SEQadmin2
Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
...-
Channel: Articles
07-09-2026, 11:10 AM -
-
by SEQadmin2
Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.
There is no single reason why many patients don’t respond to treatment as expected. Cancer is...-
Channel: Articles
07-08-2026, 05:17 AM -
-
by GATTACATLove this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
-
Channel: Articles
07-01-2026, 11:43 AM -
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, 07-13-2026, 10:26 AM
|
0 responses
20 views
0 reactions
|
Last Post
by SEQadmin2
07-13-2026, 10:26 AM
|
||
|
Started by SEQadmin2, 07-09-2026, 10:04 AM
|
0 responses
30 views
0 reactions
|
Last Post
by SEQadmin2
07-09-2026, 10:04 AM
|
||
|
Started by SEQadmin2, 07-08-2026, 10:08 AM
|
0 responses
20 views
0 reactions
|
Last Post
by SEQadmin2
07-08-2026, 10:08 AM
|
||
|
Started by SEQadmin2, 07-07-2026, 11:05 AM
|
0 responses
34 views
0 reactions
|
Last Post
by SEQadmin2
07-07-2026, 11:05 AM
|
Comment