Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • fanwei
    replied
    Originally posted by Jetse View Post
    How did you solve it?
    So other people who find this thread with the same problem can try your solution too...

    It is due to file format error caused by newline character.
    And your suggestions are also really important!

    Leave a comment:


  • Jetse
    replied
    How did you solve it?
    So other people who find this thread with the same problem can try your solution too...

    Leave a comment:


  • fanwei
    replied
    Originally posted by Jetse View Post
    It could be your computer ran out of memory, then sorting would solve your problem.

    From the manual:
    It has been resolved.Thank you!

    Leave a comment:


  • fanwei
    replied
    Originally posted by Jetse View Post
    It could be your computer ran out of memory, then sorting would solve your problem.

    From the manual:
    I have tried it,but it doesn't work.
    Any other suggestions?

    Leave a comment:


  • Jetse
    replied
    It could be your computer ran out of memory, then sorting would solve your problem.

    From the manual:
    Note
    If you are trying to intersect very large files and are having trouble with excessive memory usage, please presort your data by chromosome and then by start position (e.g., sort k1,1 -k2,2n in.bed > in.sorted.bed for BED files) and then use the -sorted option. This invokes a memory-efficient algorithm designed for large files.

    Leave a comment:


  • fanwei
    replied
    Originally posted by Jetse View Post
    What is your output when you use the command:
    Code:
    bedtools intersect -a A.bed -b B.bed -wao | less
    Do you see a lot of output, all with a zero at the end? (this means they don't have overlaps)
    There was nothing even zero.
    But it works when i write some data in new files to test that.
    Is it necessary to sort my data?

    Leave a comment:


  • Jetse
    replied
    What is your output when you use the command:
    Code:
    bedtools intersect -a A.bed -b B.bed -wao | less
    Do you see a lot of output, all with a zero at the end? (this means they don't have overlaps)

    Leave a comment:


  • fanwei
    replied
    Originally posted by Jetse View Post
    What is the command you used?
    How do the files look like?
    I used bedtools intersect -a A.bed -b.B.bed
    The first few lines are as follows,
    Click image for larger version

Name:	A.png
Views:	1
Size:	10.7 KB
ID:	304292

    Click image for larger version

Name:	B.png
Views:	1
Size:	13.5 KB
ID:	304293

    Leave a comment:


  • Jetse
    replied
    What is the command you used?
    How do the files look like?

    Leave a comment:


  • fanwei
    started a topic Error with BEDTools

    Error with BEDTools

    Dear all,
    I want your help!
    I want to use bedtools to calculate the overlap between two bed format files.It recorded chromosome,startposition and endposition informations.
    When i run bedtools, there was no error indicated and no results displayed. But i'm sure overlaps exist!
    Maybe bedtools restricted the file size?
    I feel confused. Can you kindly help me?

Latest Articles

Collapse

  • SEQadmin2
    Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
    by SEQadmin2



    Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
    ...
    07-09-2026, 11:10 AM
  • SEQadmin2
    Cancer Drug Resistance: The Lingering Barrier to Rising Survival
    by SEQadmin2



    Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

    There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
    07-08-2026, 05:17 AM
  • GATTACAT
    Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
    by GATTACAT
    Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
    07-01-2026, 11:43 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, Today, 10:26 AM
0 responses
9 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-09-2026, 10:04 AM
0 responses
24 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-08-2026, 10:08 AM
0 responses
16 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-07-2026, 11:05 AM
0 responses
33 views
0 reactions
Last Post SEQadmin2  
Working...