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Hi,
I am doing RNA-seq analysis on plants of different stresses.
My topic is In Silico Analysis of Carotenoid Metabolism Regulatory Genes in Plants in Response to Different Developmental and Environmental Conditions. I actually couldn't figure out the processes to continue and complete my thesis research.
I searched total 8 plants Arabidopsis thalaiana (Salt stress) ,Sorghum bicolor (Drought stress) ,Glycine max(Mild drought stress), Oryza sativa japonica(Alkaline stress), Solanum tuberosum(Drought stress), Setaria viridis(Salt stress), Brachypodium distachyon(Drought stress), Hordeum vulgare(Heat stress). I uploaded genome file and annotation file in fasta and gtf .gz format together with the SRR files in fastq.gz format. I am doing it on galaxy. the pipeline I followed is fastqc, then multiqc, then trimgalore, then hisat2, then featurecounts, and deseq2.
What can I do after the step of deseq? I got featurecounts datas and deseq2 plots and results file already. Now I have left to
- Extract Carotenoid Metabolism Genes from DEGs
- Functional Enrichment Analysis (GO/KEGG Pathway)
- Phylogenetic Analysis of Carotenoid Regulatory Genes
- Motif Discovery and Conserved Domain Analysis
I am not pro in using R or ubuntu still I have to finish it in short time but got no time to learn thoroughly . what tools do I need to install and commands to run the code through R or ubuntu(wsl).
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Where did you copy-paste this post from? It looks like you inadvertently included something that shows that this was copy pasted.
While not "commands to run the code through R" it would be beneficial to take a look at
DESeq2vignette that explains everything related to DE analysis: https://www.bioconductor.org/packages/release/bioc/vignettes/DESeq2/inst/doc/DESeq2.htmlThank you. Now I am able to get some plots as my output through R. Still learning.