Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • BioLion
    Junior Member
    • Apr 2014
    • 6

    #1

    StringTie merge- can someone help me understand its output?

    Hello,

    I am currently using StringTie merge on a StringTie output in order to discover genes that are not already in my reference annotation. I tried looking at the documentation but it is not very clear to me how to distinguish some things in the output or how it proceeds.

    The command I have been using is :
    Code:
    ${stringtie} --merge -G reference.gtf -o genome.StringTie.merged.gtf -F 1 -l GenomeX GenomeX.StringTie.sorted.gtf
    with GenomeX.StringTie.sorted.gtf the output of stringTie.

    I do not exactly understand how it works: when it finds a region which maps or overlaps, does it replace the line from "GenomeX..." by the line from "reference.gtf"?
    Also, what is the difference with this command?

    Code:
    ${stringtie} --merge -o genome.StringTie.merged.gtf -F 1 -l GenomeX listGenomes.gtf
    with listGenomes.gtf being:
    "reference.gtf
    GenomeX.StringTie.sorted.gtf"

    When I looked at the output of the second command, I did not see how we can distinguish between "reference.gtf" lines and "GenomeX.StringTie.sorted.gtf", or which field I am supposed to look at. Is there a way to do so after a merge?Also, does it choose between the two files when a region is similar?


    Thanks a lot for reading me,

    BioLion

Latest Articles

Collapse

  • SEQadmin2
    Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
    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
    ...
    07-31-2026, 11:01 AM
  • SEQadmin2
    Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
    by SEQadmin2


    Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

    The systematic characterization of the human proteome has
    ...
    07-20-2026, 11:48 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, 08-13-2026, 12:22 PM
0 responses
27 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 08-11-2026, 10:35 AM
0 responses
22 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 08-06-2026, 07:41 AM
0 responses
36 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 08-03-2026, 10:13 AM
0 responses
51 views
0 reactions
Last Post SEQadmin2  
Working...