Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • rxzlmn
    Junior Member
    • Nov 2013
    • 8

    #1

    very basic questions about bedtools multicov

    Hi,

    I am trying to count reads from BAM files in specific BED features using bedtools multicov.

    If I use the standard parameters (i.e. just -bams x.bam y.bam -bed x.bed), it works as expected.

    However, I have problems with the parameters for overlap, -f and for strandedness, -s/-S.

    With the settings to -s (enforcing same strand), I get 0 counts. With the inverted -S, I get counts. Since I am using datasets that have been generated with dUTP first strand method, is this expected? Cufflinks assembles the correct orientations of my transcripts with --fr-firststrand.

    For the overlap, since my bed files contain exons, I want to exclude reads from pre-mRNA that span intron-exon, therefore I set the overlap to 100% with -f 1. However, this will result in 0 counted reads. Do I misunderstand the -f setting? I only want to count reads that are 100% within the BED features of interest. I have paired-end data, so I use the -split option.

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, 08-06-2026, 07:41 AM
0 responses
15 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 08-03-2026, 10:13 AM
0 responses
31 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-31-2026, 02:55 AM
0 responses
41 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-24-2026, 12:17 PM
0 responses
26 views
0 reactions
Last Post SEQadmin2  
Working...