Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • soap2 PE results do not match bowtie or novoalign

    Hi,

    Here are the two fasta files:


    cat 0000002435.1.fa
    >0000002435
    CTGGCCAACATGGTGAAACC
    cat 0000002435.2.fa
    >0000002435
    ATCATTTAGCTGACTGGAAG

    Both novoalign and bowtie show unique and exact hit on chromosome 1, with insert distances in the 300-700 bp range. Strand orientation is fr.

    $ grep 0000002435 ../bowtie/250000.out.bt
    0000002435/1 + gi|89161185|ref|NC_000001.9|NC_000001 70750 CTGGCCAACATGGTGAAACC IIIIIIIIIIIIIIIIIIII 0
    0000002435/2 + gi|89161185|ref|NC_000001.9|NC_000001 71054 CTTCCAGTCAGCTAAATGAT IIIIIIIIIIIIIIIIIIII 0

    $ grep 0000002435 ../novo/250000.out.novo
    >0000002435 L CTGGCCAACATGGTGAAACC . U 0 11 >gi|89161185|ref|NC_000001.9|NC_000001 70751 F . 71055 R
    >0000002435 R ATCATTTAGCTGACTGGAAG . U 0 11 >gi|89161185|ref|NC_000001.9|NC_000001 71055 R . 70751 F

    soap2 -a 0000002435.1.fa -b 0000002435.2.fa -D hs_ref_36.3.fa.index -o 0000002435.out -u 0000002435.unmap -M0 -l20 -r0 -m 300 -x 720 -2 0000002435.unp -p8 -v0 2>0000002435.err

    $ cat 0000002435.err

    Begin Program SOAPaligner/soap2
    Wed Jan 26 14:30:46 2011
    Reference: hs_ref_36.3.fa.index
    Query File a: 0000002435.fr.1.fa
    Query File b: 0000002435.fr.2.fa
    Output File: 0000002435.out
    0000002435.unp
    0000002435.unmap
    Load Index Table ...
    Load Index Table OK
    Begin Alignment ...
    2 ok 0.01 sec
    Total Pairs: 1 PE
    Paired: 0 ( 0.00%) PE
    Singled: 1 (50.00%) SE
    Total Elapsed Time: 11.47
    - Load Index Table: 11.40
    - Alignment: 0.08

    SOAPaligner/soap2 End
    Wed Jan 26 14:30:58 2011

    Thanks for any ideas.
    Susan

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
53 views
0 likes
Last Post seqadmin  
Working...
X