Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • paolo.kunder
    Member
    • Aug 2011
    • 93

    BAM record error: found spliced alignment without XS attribute

    Dear All,
    I have browsed old forums but I really don't know how to fix problem,
    I mapped SOLiD reads with LifeScope, then I run both cufflinks and cuffmerge, now when I run cuffdiff I encounter the XS tag problem, how do i fix it?
    any experience?

    from cufflinks web site:

    However Cufflinks will accept SAM alignments generated by any read mapper. Here's an example of an alignment Cufflinks will accept:
    and what about cuffdiff?

    thanks,
    paolo


    samfile:
    Code:
    691_1862_244    16      chr1    3000885 1       5S25M20S        *       0       0       CTGCGGGCATTNNGTACCATGCGGNNNGGGTAATAACGGAAATAATTGTA      ...367...-+%(
    CFFJJJJJJ?3*#'+,,52222222221111112444   RG:Z:SHAM_1     NH:i:1  CM:i:2  NM:i:0  CQ:Z:/?;//@@@//;@;6666@@/?>6/22//2@@2/<2@@/26@@?@=@62@@ CS:Z:T031103033002031
    03303100010003313101310110313003312
    426_2037_1220   16      chr1    3034383 1       5S25M3S17H      *       0       0       GACAGTCTTTTAAGCCCGTGGTTGTGTCTNCGN       //4559:::9088GAJJJJJJJJJJHFF2
    )1+'    RG:Z:SHAM_1     NH:i:1  CM:i:2  NM:i:3  CQ:Z:/@@@22@/88/@<8@/@//2@//@2/6/@=6@/6>6>/@;/@;@28@=2< CS:Z:T32223212221022230133202211110101130032030002212
    112
    670_1721_1819   0       chr1    3063656 5       20S27M3S        *       0       0       CCCCCCACTTTGAGGGTTTCACAAACAGAGGCATAAGGNNNNAGTGTCNN      >644444444444
    6888<AE>>DJJJJJJJJJJJJ:90$&$&+577?-*)   RG:Z:SHAM_1     NH:i:1  CM:i:2  NM:i:0  CQ:Z:6//@=6@/@=6?@/2@@26;@@//6=@/@@@2@8?/@/*/</2.2@@//2 CS:Z:T200000112001220
    01002111001122203133020200232111200
    Last edited by paolo.kunder; 09-06-2012, 06:13 AM.

Latest Articles

Collapse

  • GATTACAT
    Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
    by GATTACAT
    Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
    07-01-2026, 11:43 AM
  • SEQadmin2
    Nine Things a Sample Prep Scientist Thinks About Before Sequencing
    by SEQadmin2


    I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

    Here are nine questions we think about, in roughly the order they matter, before...
    06-18-2026, 07:11 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, 07-02-2026, 11:08 AM
0 responses
22 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 06-30-2026, 05:37 AM
0 responses
23 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 06-26-2026, 11:10 AM
0 responses
22 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 06-17-2026, 06:09 AM
0 responses
55 views
0 reactions
Last Post SEQadmin2  
Working...