Anyone here using Agilent SS All Exon V7 kit? I'm continuously getting low yield around 2-3 nM with 100ng input. Any suggestions?
Unconfigured Ad
Collapse
X
-
SS XT Low Input has a similar workflow to HS. After library prep, 1000 ng was inputted into hybridization. Other places where I see can affect yield is lost of the capture beads during the washing step.
Are these the same samples as your test run? They could be DNA of poorer quality.
Comment
-
Thanks a lot for your reply. Have you done the SS All Exon V7 dual index library or with MBC? Because the yield with the MBC is ranging from 4-10 nM and for the dual index libraries it goes down to half (1-3nM).Surprisingly, they are consistent throughout the samples. We are working with the Agilent tech support on site and we haven't figured out the explanation yet!!
Comment
-
It was with the MBC. You could increase the post-capture PCR cycle by 1 but you might see higher PCR duplicate reads during analysis. I'm curious to see if there are any differences in the sample metrics (% on-target, % duplicates, etc.) and variant calling between the MBC and dual index.
Comment
-
Did you get your answer from Agilent Tech Support so far? I am experiencing the same issue using the SureSelect HS with dual-index.Originally posted by baru View PostThanks a lot for your reply. Have you done the SS All Exon V7 dual index library or with MBC? Because the yield with the MBC is ranging from 4-10 nM and for the dual index libraries it goes down to half (1-3nM).Surprisingly, they are consistent throughout the samples. We are working with the Agilent tech support on site and we haven't figured out the explanation yet!!
Cheers
Comment
-
Hello! I'm sorry I missed your query. Well, I did a couple of optimization like increasing the bead capture to 1 hr and reducing the elution volume to 20 ul. Yield slightly improved. So we sequenced them anyway on an SP flow cell before moving with our larger sets of samples. Exome quality was extremely good in the end. So don't worry about the yield, as long your libraries are of good quality go ahead and sequence them
ps: This is just my experience
Comment
Latest Articles
Collapse
-
by SEQadmin2
Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?
Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating...-
Channel: Articles
10-14-2026, 09:55 AM -
-
by SEQadmin2
Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.
We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing...-
Channel: Articles
-
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, 10-15-2026, 10:52 AM
|
0 responses
14 views
0 reactions
|
Last Post
by SEQadmin2
10-15-2026, 10:52 AM
|
||
|
Started by SEQadmin2, 10-14-2026, 05:39 AM
|
0 responses
21 views
0 reactions
|
Last Post
by SEQadmin2
10-14-2026, 05:39 AM
|
||
|
Started by SEQadmin2, 10-13-2026, 09:56 AM
|
0 responses
19 views
0 reactions
|
Last Post
by SEQadmin2
10-13-2026, 09:56 AM
|
||
|
Started by SEQadmin2, 10-09-2026, 11:14 AM
|
0 responses
27 views
0 reactions
|
Last Post
by SEQadmin2
10-09-2026, 11:14 AM
|
Comment