Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • about uniprot sprot.fasta header

    hey guys,
    i wanna ask a question about uniprot fasta file header.

    in the header shown as below:

    Code:
    kurban@kurban-X550VC:~/Desktop/Uniprot$ zcat uniprot_sprot.fasta.gz | more
    [COLOR="Blue"]>sp|Q6GZX4|001R_FRG3G Putative transcription factor 001R OS=Frog virus 3 (isolate Goorha) GN=FV3-001R PE=4 SV=1[/COLOR]
    MAFSAEDVLKEYDRRRRMEALLLSLYYPNDRKLLDYKEWSPPRVQVECPKAPVEWNNPPS
    EKGLIVGHFSGIKYKGEKAQASEVDVNKMCCWVSKFKDAMRRYQGIQTCKIPGKVLSDLD
    AKIKAYNLTVEGVEGFVRYSRVTKQHVAAFLKELRHSKQYENVNLIHYILTDKRVDIQHL
    EKDLVKDFKALVESAHRMRQGHMINVKYILYQLLKKHGHGPDGPDILTVKTGSKGVLYDD
    SFRKIYTDLGWKFTPL
    Code:
    kurban@kurban-X550VC:~/Desktop/Uniprot$ zcat uniprot_trembl.fasta.gz | more
    [COLOR="Blue"]>tr|G9CT51|G9CT51_9ARCH Ammonia monooxygenase (Fragment) OS=uncultured ammonia-oxidizing archaeon GN=amoA PE=4 SV=1[/COLOR]
    CTHYLFIVVVAVNSTLLTINAGDYIFYTDWAWTSFTVFSISQTLMLIVGACYYLTFTGVP
    GTATYYALIMTVYTWVAKAAWFSLGYPYDFIVTPVWLPSAMLLDLVYWATKKNKHSLILF
    GGVLVGMSLPLFNMVNLITVADPLETAFKYPRPTLPPYMTPIEPQVGKFYNSPVALGAGA
    GAVLGCTFAALGCKLNT
    which ones are UniProt IDs and which ones are Uniprot accession numbers?
    Last edited by kurban910; 12-01-2015, 02:41 PM.

  • #2
    see http://www.uniprot.org/help/differen...sion_entryname

    The first set of identifiers (Q6GZX4, G9CT51) are the accession numbers.

    Comment


    • #3
      thanks you @mastal.

      Comment


      • #4
        How to Run BBmap for many .fastaq files?

        #!/bin/bash
        ./bbmap.sh ref=ref.fa # creating index file from the input reference
        for i in {ls*.fastq}
        do
        ./bbmap.sh in=i out={.}
        done


        I also tried using GNU parallel ls *.sra | xargs -I {} -P 5 -n 1 ./fastq-dump {}| ./bbmap.sh in=ls *.fastq out=mapped.sam

        (sra part works, bbmap not)
        what to change in code?
        Last edited by Mat29; 01-01-2016, 11:14 AM.

        Comment

        Latest Articles

        Collapse

        • seqadmin
          Current Approaches to Protein Sequencing
          by seqadmin


          Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
          04-04-2024, 04:25 PM
        • seqadmin
          Strategies for Sequencing Challenging Samples
          by seqadmin


          Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
          03-22-2024, 06:39 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by seqadmin, 04-11-2024, 12:08 PM
        0 responses
        30 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-10-2024, 10:19 PM
        0 responses
        32 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-10-2024, 09:21 AM
        0 responses
        28 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-04-2024, 09:00 AM
        0 responses
        52 views
        0 likes
        Last Post seqadmin  
        Working...
        X