Redundancy reduction of de novo transcriptome assemblies with Compacta?

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I've been sweating over how best to reduce the redundancy in a de novo transcriptome assembled using Trinity. I found this tool called Compacta (here's the GitHub repository) that seems to be aimed at solving precisely this problem.

Can anyone comment/share their thoughts on this tool? Has anybody used it before? I haven't really found any papers citing it (yet).


de-novo


transcriptome


redundancy-reduction

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