I was uploading my RNA-seq assembly in TSA and I am not sure how to proceed. 743 sequences from my assembly got flagged with Code(VECTOR_MATCH) UniVec vector: gnl|uv|NGB00150.1:1-46 Ambion FirstChoice RLM-RACE 3' RACE adapter. I find it weird because I thought I already removed adapters prior to assembly using trimmomatic + fastqc. I have searched for the sequence of the adapter. What I want to know is how do I safely trim out the adapter sequence. I mean what if the vector is at the middle portion of the sequence, is it still acceptable to just remove the chunk and merge the two segments together? I could not find any sources to answer this at the moment that's why I am here.
Unconfigured Ad
Collapse
Latest Articles
Collapse
-
by SEQadmin2
NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification,...-
Channel: Articles
10-30-2026, 06:46 AM -
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, Yesterday, 07:59 AM
|
0 responses
18 views
0 reactions
|
Last Post
by SEQadmin2
Yesterday, 07:59 AM
|
||
|
Started by SEQadmin2, 11-05-2026, 09:25 AM
|
0 responses
32 views
0 reactions
|
Last Post
by SEQadmin2
11-05-2026, 09:25 AM
|
||
|
Started by SEQadmin2, 11-03-2026, 11:54 AM
|
0 responses
47 views
0 reactions
|
Last Post
by SEQadmin2
11-03-2026, 11:54 AM
|
||
|
Genome Sequencing Reveals Large, Repeat-Rich DNA in Trapdoor Spider Named for Stephen Colbert
by SEQadmin2
Started by SEQadmin2, 10-28-2026, 09:57 AM
|
0 responses
172 views
0 reactions
|
Last Post
by SEQadmin2
10-28-2026, 09:57 AM
|