Hello guys, I am new in transcriptomic analysis. I am using tophat for mapping MACE reads (Massive analysis of 3' cDNA ends) in the wheat genome. I am analyzing salt-stressed and control samples. I have realized that some reads do map to chloroplast and mitochondrial sequences in the reference... and as far as i have understood the libraries preparation consider polyA capture. I think that I should keep this reads, but i am not really sure if its better only mapping to the nuclear genome. I want to hear more opinions, and advices and additional considerations about this issue, thank you very much for your help.
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CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).
Despite this, “CRISPR helped turn genome editing from a specialized technique into...07-31-2026, 11:01 AM