Hi All,
I have a question: for a relatively "good" FastQC report, do we still need to do data pre-processing?
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What we can learn from FastQC reports
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Is a compositional bias in Sequence Content of initial bases in WES reads normal?
Per Base Sequence Content
Any experienced Whole Exome Sequencing analyst/experimentalist:
the Per Base Sequence Content...
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fastqc shows strange GC content
Hi,
we have a 36-samples ChIP-Seq experiment with a very strange GC-content behavior (s. images)
The samples are from yeast. This...
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Opinion on FastQC output for HiSeq 4000 PE sequencing run
Hello,
I recently had four 400bp insert plant DNA libraries sequenced (2x150bp) using one HiSeq 4000 lane.
I've attached...Last edited by quokka; 07-30-2018, 06:45 PM. Reason: remove identifying information from attachments
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FastQC results for 16s reads
Hi
I have some FastQC results I have generated from Illumina 16s sequences. I have attached an example of the results for one of the demultiplexed...
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Problem with trimming after FastQC
Hi,
After using a FastQC I noticed that I have red flags in Per base sequence content and in Per base content.
I used Trimmomatic...
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low GC% peak in one end of paired end reads
Hi,
I have paired end RNA seq data prepared from Brassica napus using TruSeq kit. After adapter trimming, FastQC shows a second low GC% peak per...
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Fastqc
Dear members.
I am using FASTQC* for the first time (in Galaxy).
Is there an online resource showing how to deal with a range of RNAseq...
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FastQC, v0.11.5, error: Too many tiles ...
Ubuntu
Hi,
I have FastQC, v0.11.5 and I want to evaluate an Illumina run (pairend). I have reads of 150bp and a average...
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5' Kmers problem with whole genome re-sequencing data
Hi all,
I am having some issues with getting rid of kmers in my sequencing data sets. We have re-sequenced several African buffalo genomes...
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Fastqc Per sequence quality scores - Two peaks?
Hi,
I am struggling to find possible explanations for seeing two distinct peaks in my "per sequence quality scores". I am very...