Question: miRNA seq data TRIMMOMATIC
0
gravatar for aangajala
6 months ago by
aangajala0
aangajala0 wrote:

I am trying to analyze microRNA sequencing data for 8 datasets ( each dataset is a cell line). I am able to run FASTQC and Multi-QC. Single end data.Per sequence quality, 8/8 passed. Sequence duplication level 8/8 failed.Persequence GC content 8 failed. So When I tried to use TRIMMOMATIC, it is showing error in the collection. Please advice. here is the error message Picked up _JAVA_OPTIONS: -Djava.io.tmpdir=/galaxy-repl/main/jobdir/018/565/18565857/_job_tmp -Xmx7g -Xms256m TrimmomaticSE: Started with arguments: -threads 1 -phred33 fastq_in.fastqsanger fastq_out.fastqsanger SLIDINGWINDOW:4:20 Exception in thread "m

fastq sra ncbi rna-seq fastqsanger • 245 views
ADD COMMENTlink modified 6 months ago by Jennifer Hillman Jackson25k • written 6 months ago by aangajala0
0
gravatar for Jennifer Hillman Jackson
6 months ago by
United States
Jennifer Hillman Jackson25k wrote:

Hello,

I am not sure how you extracted/manipulated the data before uploading it, but it has a formatting problem. The line count is not correct for fastq data (must be a multiple of 4) and at least one sequence is has a problematic sequence identifier (the "@" is missing). Not all tools result in an error using this input, but many will. It is best to get a clean copy of the source fastq data.

To extract these reads directly into Galaxy, use the tool NCBI SRA Tools > Download and Extract Reads in FASTA/Q format from NCBI SRA. All you need to enter on the tool form is the accession number.

Support FAQs: https://galaxyproject.org/support/#getting-inputs-right

Thanks! Jen, Galaxy team

ADD COMMENTlink written 6 months ago by Jennifer Hillman Jackson25k

Thanks so much, when i tried using SRA NCBI upload.it worked.Thanks.

ADD REPLYlink written 6 months ago by aangajala0
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