Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • gary
    Member
    • Dec 2009
    • 16

    GATK depthofcoverage problem

    Hi

    I am using GATK depthofcoverage to calculate my exome-seq data:

    Code:
     nohup java -jar ~/GATK/GenomeAnalysisTK-1.3-23-g13905c0/GenomeAnalysisTK.jar \
    -T DepthOfCoverage -o depthofcoverage_sample1 -I Sample_1.bam \
    -ct 10 -ct 20 -ct 30 -R hg19.fa -geneList Genome_UCSC.refseq -omitBaseOutput &
    But the output file depthofcoverage_sample1.sample_gene_summary is empty.

    I thought it was because I didn't sort my refseq file, whose first few lines are as follow:

    Code:
    #bin    name    chrom   strand  txStart txEnd   cdsStart        cdsEnd  exonCount       exonStarts      exonEnds        score   name2   cdsStartStat    cdsEndStat      exonFrames
    0       NM_032291       chr1    +       66999824        67210768        67000041        67208778        25      66999824,67091529,67098752,67101626,67105459,67108492,67109226,67126195,67133212,67136677,67137626,67138963,67142686,67145360,67147551,67154830,67155872,67161116,67184976,67194946,67199430,67205017,67206340,67206954,67208755,       67000051,67091593,67098777,67101698,67105516,67108547,67109402,67126207,67133224,67136702,67137678,67139049,67142779,67145435,67148052,67154958,67155999,67161176,67185088,67195102,67199563,67205220,67206405,67207119,67210768,       0       SGIP1   cmpl    cmpl    0,1,2,0,0,0,1,0,0,0,1,2,1,1,1,1,0,1,1,2,2,0,2,1,1,
    1       NM_001080397    chr1    +       8384389 8404227 8384389 8404073 8       8384389,8385357,8385877,8390268,8395496,8397875,8399552,8403806,        8384786,8385450,8386102,8390996,8395650,8398052,8399758,8404227,        0       SLC45A1 cmpl    cmpl    0,1,1,1,0,1,1,0,
    So I downloaded the GATK sortByRef.pl file and typed the following command:

    Code:
     perl SortByRef.pl Genome_UCSC.refseq ~/ref/UCSC/hg19/hg19.fa.fai
    then I got an error:
    Code:
    Can not open temporary file 1045: Too many open files at SortByRef.pl line 95, <$INPUT> line 1021.
    What am I doing wrong?
    Last edited by gary; 07-01-2012, 05:17 PM.

Latest Articles

Collapse

  • 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
  • SEQadmin2
    From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
    by SEQadmin2


    Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


    The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
    ...
    06-02-2026, 10:05 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, 06-26-2026, 11:10 AM
0 responses
12 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 06-17-2026, 06:09 AM
0 responses
48 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 06-09-2026, 11:58 AM
0 responses
107 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 06-05-2026, 10:09 AM
0 responses
125 views
0 reactions
Last Post SEQadmin2  
Working...