A while back ECO posted some great info on a 1x300 miseq run. Has anybody tried a similar run with an upgraded instrument to achieve a 500 nt read? Will the software permit this? How do the base qualities trail off?
Unconfigured Ad
Collapse
X
-
I dont see how it would. If the sum of your amplicon is shorter than that of your paired ends you can join them based on a region of overlap
-
The 1x300 runs you are referring to were likely done with v.1 kits?Originally posted by bbeitzel View PostWe've done several 1x300 runs with 300 cycle kits, and there is a noticeable dropoff in quality after ~base 250 on good runs. I can't imagine that a 1x500 run would give you more than ~300 bases of usable data.
It is great if koadman is willing to sacrifice a v.2 kit and enlighten all on two things: if the 1 x 500 will work and where the drop-off in qualities can be expected to start.
Comment
Latest Articles
Collapse
-
by SEQadmin2
CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).
Despite this, “CRISPR helped turn genome editing from a specialized technique into...-
Channel: Articles
07-31-2026, 11:01 AM -
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, 08-24-2026, 10:32 AM
|
0 responses
33 views
0 reactions
|
Last Post
by SEQadmin2
08-24-2026, 10:32 AM
|
||
|
Started by SEQadmin2, 08-20-2026, 11:17 AM
|
0 responses
42 views
0 reactions
|
Last Post
by SEQadmin2
08-20-2026, 11:17 AM
|
||
|
Started by SEQadmin2, 08-18-2026, 10:05 AM
|
0 responses
45 views
0 reactions
|
Last Post
by SEQadmin2
08-18-2026, 10:05 AM
|
||
|
Started by SEQadmin2, 08-13-2026, 12:22 PM
|
0 responses
49 views
0 reactions
|
Last Post
by SEQadmin2
08-13-2026, 12:22 PM
|
Comment