Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • bye
    Junior Member
    • Sep 2010
    • 8

    #1

    bowtie2, option -N

    We have SE 100bp reads aligned with bowtie2. We noticed that when keep other options the same, but change -N 0 to -N 1, we got some really different alignments, see example below:
    Code:
    bowtie2 -x ./hg19/hg19_all --end-to-end -D 20 -R 3 -N 0 -L 20 -i S,1,0.50 --score-min L,-1,-1 -c AGAGCTGTTCCTATTCGGCCATCTTGGCTCCTCCTCCCGGATTCACTGATTTTTTGAAGGGTTTTTTGTGTCTCTATCTCCTTCAGTTCTGCTCTGATCTT
    Output:
    Code:
    0       0       chr4    58434477        42      101M    *       0       0       AGAGCTGTTCCTATTCGGCCATCTTGGCTCCTCCTCCCGGATTCACTGATTTTTTGAAGGGTTTTTTGTGTCTCTATCTCCTTCAGTTCTGCTCTGATCTT  IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII  AS:i:-12        XN:i:0  XM:i:2  XO:i:0  XG:i:0  NM:i:2  MD:Z:0G72T27    YT:Z:UU
    Code:
    bowtie2 -x ./hg19/hg19_all --end-to-end -D 20 -R 3 -N 1 -L 20 -i S,1,0.50 --score-min L,-1,-1 -c AGAGCTGTTCCTATTCGGCCATCTTGGCTCCTCCTCCCGGATTCACTGATTTTTTGAAGGGTTTTTTGTGTCTCTATCTCCTTCAGTTCTGCTCTGATCTT
    Output:
    Code:
    0       16      chr2    136138378       0       60M5I1M1I34M    *       0       0       AAGATCAGAGCAGAACTGAAGGAGATAGAGACACAAAAAACCCTTCAAAAAATCAGTGAATCCGGGAGGAGGAGCCAAGATGGCCGAATAGGAACAGCTCT  IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII  AS:i:-88        XN:i:0  XM:i:10 XO:i:2  XG:i:6  NM:i:16 MD:Z:13C11C3A8C18T5C2T0T11A14C0
            YT:Z:UU
    I'm confused about the results. I thought -N 1 should be able to pick up the best alignment with -N 0, how come the alignment results are so much worse when -N 1 for the same read?

    Thanks in advance!

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, Yesterday, 10:35 AM
0 responses
7 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 08-06-2026, 07:41 AM
0 responses
24 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 08-03-2026, 10:13 AM
0 responses
43 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-31-2026, 02:55 AM
0 responses
48 views
0 reactions
Last Post SEQadmin2  
Working...