Hi
I also use tophat to map RNA-seq data, and I have some questions, does the tag NH:i:1 work for pair-ended reads? Or it just concerns one mate read?
I mean, if I accept all alignments which have the tag NH:i:1, could I be sure that specific pairs which can be alined only one time, are all selected?
In other words, is it possible one mate has "NH:i:1", an the other mate has "NH:i:3"?
Unconfigured Ad
Collapse
X
-
Hope this is not too late to ask a question on this topic.
Is it the right way to extract unique-reads by just simply basing on the read name in SAM/BAM file (after filtering out reads having no reported alignments, i.e. samtools view -F4) ? It means a read is called unique-mapped if its name occurs exactly one time (for single-end). I asked this because I were afraid that different aligners use different ways to report mapping quality.
Leave a comment:
-
Mapping quality of zero usually means the mapping could not be unambiguously placed, which is likely in repeat regions.
Leave a comment:
-
I figure out: using grep -w or awk.
Another question : lots of reads (mapping quality=0) are aligned to reapeted region in my RNA-seq data. what does this mean?
Leave a comment:
-
After checking the results, I found using grep "XH:i:1" I mistook the reads with "XH:i:1**", see the example:Originally posted by nilshomer View PostWhat is the alignment score (AS tag) for those mapq = 0 reads? Can you post one record?
2045_1360_1504_F5-BC 409 chr7 3155885 0 25M * 0 0 AAAAGGGGGAAGGGAAAGAGGGAGG 004DI:.""-,*"'/);LRYMDNCC NM:i:0 NH:i:10CC:Z:= CP:i:70303403 XS:A:+ HI:i:8
So what is the script which I can extract "XH:i:1" ?
Leave a comment:
-
What is the alignment score (AS tag) for those mapq = 0 reads? Can you post one record?
Leave a comment:
-
Question on mapping quality and uniquely mapped read
Dear all.
I use tophat to map RNA-seq data. After getting results, I use two ways to filter the alignment. one is using grep "NH:i:1" to get uniquely mapping reads; the other is using samtools view -bq to get reliable reads. However, I found many uniquely mapped reads have mapping quality =0. How to explain it?
It's a single-end data.Tags: None
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, Yesterday, 11:13 AM
|
0 responses
21 views
0 reactions
|
Last Post
by SEQadmin2
Yesterday, 11:13 AM
|
||
|
Started by SEQadmin2, Yesterday, 10:48 AM
|
0 responses
18 views
0 reactions
|
Last Post
by SEQadmin2
Yesterday, 10:48 AM
|
||
|
Started by SEQadmin2, 10-15-2026, 10:52 AM
|
0 responses
36 views
0 reactions
|
Last Post
by SEQadmin2
10-15-2026, 10:52 AM
|
||
|
Started by SEQadmin2, 10-14-2026, 05:39 AM
|
0 responses
42 views
0 reactions
|
Last Post
by SEQadmin2
10-14-2026, 05:39 AM
|
Leave a comment: