Question: Can you see what i got problem??
gravatar for cucucucoco
7 months ago by
cucucucoco0 wrote:

I did uproading file through EBI homepage about NCBI Geo dataset SRR 5682257 &5682258. [EBI SRA: SRX2917412 File:] and it was convert using FASTQ Groomer Tool (convert between various FASTQ quality formats) at NGS: QC and manipulation. because first file is gz file that are compressed file. next, i did click FastQC Tool (Read Quality reports), so that i see Quality control of this dataset.

unfortunately, per tile sequence quality and sequence Duplication levels got X. i am user who use Galaxy tool first time for analysis NCBi dataset. so i am poor.

In this case, Is this data sets already finished Trimming by original uproader?? so am i just have to start analysis alingment using Bowtie ? other wise, IS this dataset' Quality very low?

what i have got problem T-T... please help me.

quality control fastqc galaxy • 199 views
ADD COMMENTlink modified 7 months ago by Jennifer Hillman Jackson24k • written 7 months ago by cucucucoco0
gravatar for Jennifer Hillman Jackson
7 months ago by
United States
Jennifer Hillman Jackson24k wrote:


Reviewing these FAQs and tutorials will help you to understand the workflow for QA and data prep (plus more).

In summary, it is best to upload data, run FastQC, review the results to determine the quality score format, convert with the Groomer tool (only if needed) or directly assign the fastqsanger datatype, run FastQC again if you ran Groomer, assess quality, Trim/filter as needed with (Trimmomatic, Trim Galore!), FastQC again to review how the QA changed the data (you might want to try a few different settings and compare to find the best options for your specific data), then proceed to map steps and downstream analysis.

Hope this helps! Jen, Galaxy team

ADD COMMENTlink written 7 months ago by Jennifer Hillman Jackson24k
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