Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts

  • huma Asif
    replied
    i want all the genes e.g in sample 1 to be concatenated as >1 likewise for my all samples
    my thought is as all genes in all files are in same order so when i have multifasta as >1, >2, >3,>4,>5
    i will take that multifasta to do alignment around these interval

    Leave a comment:


  • GenoMax
    replied
    If you rename all of them as >1 or >2 for a sample the sequences ID's would no longer be unique.

    What kind of MSA are you trying to do?

    Leave a comment:


  • huma Asif
    replied
    GenoMax
    yes

    Leave a comment:


  • HMorrison
    replied
    Originally posted by GenoMax View Post
    You want to convert every fasta ID header from multiple fasta sequences in file "a" to >1 and from file "b" to >2, is that correct?
    That won't give them unique deflines, which I think is what he/she is after for input to clustalw. I still can't tell what the problem is, though.

    Leave a comment:


  • GenoMax
    replied
    You want to convert every fasta ID header from multiple fasta sequences in file "a" to >1 and from file "b" to >2, is that correct?

    Leave a comment:


  • huma Asif
    replied
    how i can convert
    >1...>2....>3...>10000 to >1

    and
    >1..>2..>3....>10000 for b.fasta to >2 and
    same for for all my 5 samples
    i have to use this file for multiple alignment
    Last edited by huma Asif; 09-08-2014, 10:28 AM.

    Leave a comment:


  • GenoMax
    replied
    Do you want to know how to do the renaming or is this just an informational post?

    Leave a comment:


  • huma Asif
    started a topic MUltifasta file

    MUltifasta file

    hi every one,

    what i need to do is i need multiple sequence alignment file

    i converted the vcf file to consensus fasta and "cat" all these consensus sequence into multifasta.



    in my cat file seq are >1......>10000 for a.fasta and >1......>10000 for b.fasta when i use clustal w it gives error that sequence have same header THAT MAKES SENSE so what i am planning to do is to convert >1..>2...>3.>10000 to >1

    and >1..>2..>3..>10000 for b.fasta to >2 and same for for all my 5 samples
    i have to use this file for multiple alignment
    Regards
    Last edited by huma Asif; 09-08-2014, 10:13 AM.

Latest Articles

Collapse

  • SEQadmin2
    Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
    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
    ...
    10-14-2026, 09:55 AM
  • SEQadmin2
    New Genomics Technologies Take Aim at Long-Standing Limits
    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
    ...
    09-28-2026, 10:25 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, Yesterday, 11:13 AM
0 responses
15 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, Yesterday, 10:48 AM
0 responses
15 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-15-2026, 10:52 AM
0 responses
35 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-14-2026, 05:39 AM
0 responses
42 views
0 reactions
Last Post SEQadmin2  
Working...