I do have a set of data containing both Exome Seq and RNA Seq. It will be interesting to see how they correlate in terms of calling. Specifically, it will be interested to see how mark duplication will affect the concordance between the RNA samples from the DNA samples. However, I do have a question: is it valid to use tools like GATK to perform snp calling on RNA Samples? To my knowledge, it seems like GATK might contain certain prior specifically designed for exome sequencing (or whole genome sequencing). Wouldn't that also affect the call concordance in the final data?
Seqanswers Leaderboard Ad
Collapse
Announcement
Collapse
No announcement yet.
Latest Articles
Collapse
-
by seqadmin
The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...-
Channel: Articles
05-06-2024, 07:48 AM -
ad_right_rmr
Collapse
News
Collapse
Topics | Statistics | Last Post | ||
---|---|---|---|---|
Started by seqadmin, Today, 02:06 PM
|
0 responses
6 views
0 likes
|
Last Post
by seqadmin
Today, 02:06 PM
|
||
Started by seqadmin, 05-14-2024, 07:03 AM
|
0 responses
27 views
0 likes
|
Last Post
by seqadmin
05-14-2024, 07:03 AM
|
||
Started by seqadmin, 05-10-2024, 06:35 AM
|
0 responses
47 views
0 likes
|
Last Post
by seqadmin
05-10-2024, 06:35 AM
|
||
Started by seqadmin, 05-09-2024, 02:46 PM
|
0 responses
59 views
0 likes
|
Last Post
by seqadmin
05-09-2024, 02:46 PM
|
Comment