Hello everyone,

I'm currently working on analyzing RNA seq data and downloaded a fastq file from the NCBI website for practice. After using trimmomatic to trim my data, I faced challenges while attempting to align it with the human genome (hg38) using either Hisat2 or the STAR tool. Specifically, I encountered issues when running the 'make' command to build the Hisat2 executable.

I would appreciate any advice or guidance on resolving these challenges.

Thank you!

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