Hello everyone!
I am working with RNA-seq data of several human samples. I have been able now to obtain successfully a bam file from my samples after alignment with RNASTAR tool, and also obtained read counts with FeatureCounts tool.
However, now I have a problem with obtaining a normalized value for said reads that I can use to compare between genes within the same sample and among samples.
Regarding this topic I have two questions:
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Is there a tool to obtain gene FPKM counts automatically? I know the “FPKM count tool exists” however it only gives me FPKM values per transcript (ENST code in ENSEMBL) and not per gene (ENSG code). Is there a different tool that can allow me to obtain FPKM/gene?
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For data normalization would it be better to use another type of count normalization different than FPKM?
Thank you very much in advance,
Coral