Entering edit mode
3.4 years ago
santos48
▴
40
Hello everyone, I have human Rna-Seq data reading by MiniOn.I aligned with the human reference genome (GRCh38.p13) from that website= https://www.gencodegenes.org/human/ using minimap2. Then I extract specific regions on the bam file using samtools. For the starting DESeq2, I tried to featureCounts with reference annotation folder bam file %5 assigned according to multiqc report.
How to create an annotation folder for quantification?
Then I extract specific regions on the bam file using samtools.
why extract specific regions were used?
For the starting DESeq2, I tried to featureCounts with reference annotation folder bam file %5 assigned according to multiqc report.
unclear.
I extracted specific regions because of those regions I will research. I have noisy data that's why I extracted and annotated it. Then I checked results with multiqc in the results, samples assigned just %5.
as you used only a subset of the genome, the 5% mapping rate is possible, regardless of the contaminated data.