Genome Analysis Toolkit

Variant Discovery in High-Throughput Sequencing Data

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Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size. Learn more

ERROR while calling variants...

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    Manoj Kumar

    Hi I have fastq (MnION) file and a reference fasta file..I have still issue to not getting results ...... 

    --FILE 1

    @ID_5331388
    CTCCACTCTGGGATGGGAATTCTCCTCCACTCTGGGATGGGAATTCTCCTCCACTCTGGGATGGGAATTCTCCTCCACTCTGGGATGGGAATTCTCCTCC
    +ID_5331388
    AAFFFJJJFJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJFJJJJJJJJJJJJJ7FFJJJJJJJJJFJJJFJJJJJJJJJJJJJFJJJJJJJJJJJJJJJ
    @ID_6694963
    CTCCACTCTGGGATGGGAATTCTCCTCCACTCTGGGATGGGAATTCTCCTCCACTCTGGGCTGGGAATTCTCCTCCACTCTGGGATGGGCATTCTCCTCC
    +ID_6694963
    AAAFFJJJJJJJFJJJJJFJJFJJJJJJJJJJJJJJFJJJF<FJJJJJJJJJ-AJ<-AJF-7JFF7--7<7FFFJJ-<<AA-FF-<FAJ))-AF-----)

    ---FILE 2

    >KF267450.1
    TTAAAAGAGATTTTCTATCTACGGATAGTTAGCTCTTTTTCTAGACTCTTGTCTACTCAATTCAACTAAA
    CGAAATTTTGTCCTTCCGGCCGCATGTCCATGCTGCTGGAAGCTGACGTGGAATTTCATTAGGTTTGCTT

     

    --ERROR--

    A USER ERROR has occurred: Input files reference and reads have incompatible contigs: No overlapping contigs found.
    reference contigs = [KF267450.1]
    reads contigs = []

     

     

     

     

     

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