Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • slp
    Junior Member
    • Dec 2010
    • 9

    #1

    Novoalign query

    I am running into problems trying to run novoalign. We ran a 96 bp paired end exome sequencing exp. But the fastq files have reads ranging from 35-96bp (because of adapter trimming).
    Each fast file has about 10s of Millions of reads. But when I try to align the reads with the following command
    novoalign -d hg38.nix -f read1.fastq read2.fastq -o SAM > Out.sam

    only few hundred reads are processed out of the Millions of reads (Please see below). I am not sure whats going wrong here.

    Interpreting input files as Illumina FASTQ, Casava Pipeline 1.8 & later.
    # Index Build Version: 3.3
    # Hash length: 14
    # Step size: 2
    # Paired Reads: 259
    # Proper Pairs: 193 (74.5%)
    # Read Sequences: 518
    # Unique Alignment: 469 (90.5%)
    # Multi Mapped: 36 ( 6.9%)
    # No Mapping Found: 7 ( 1.4%)
    # QC Failures...
    # Read Length: 6 ( 1.2%)
    # Elapsed Time: 5.855 (secs.)
    # CPU Time: 12.41 (secs.)
    # Fragment Length Distribution
    # From To Count
    # 45 59 11
    # 60 74 18
    # 75 89 3
    # 90 104 33
    # 105 119 23
    # 120 134 19
    # 135 149 17
    # 150 164 9
    # 165 179 9
    # 180 194 7
    # 195 209 4
    # 210 224 3
    # 225 239 4
    # 240 254 3
    # 255 269 2
    # 270 284 1
    # 285 299 1
    # 300 314 2
    # 315 329 0
    # 330 344 0
    # 345 359 0
    # 360 374 0
    # 375 389 0
    # 390 404 1
    # 405 419 1
    # Mean 132, Std Dev 62.0
    # Done at Mon Nov 9 20:31:31 2015


    Any help is much appreciated.

Latest Articles

Collapse

  • kinpict.com
    Reply to 16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
    by kinpict.com
    The part about this topic feels surprisingly grounded, and the details on the page is the bit that made me slow down. I’d keep <a href="https://kinpict.com/">ai family photo generator</a> bookmarked for later.
    Today, 06:37 PM
  • SEQadmin2
    16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
    by SEQadmin2





    NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification,...
    10-30-2026, 06:46 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, 11-12-2026, 07:59 AM
0 responses
27 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 11-05-2026, 09:25 AM
0 responses
35 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 11-03-2026, 11:54 AM
2 responses
56 views
0 reactions
Last Post kinpict.com  
Started by SEQadmin2, 10-28-2026, 09:57 AM
0 responses
175 views
0 reactions
Last Post SEQadmin2  
Working...