Hello everyone,
I have a number of single-ended samples generated by Illumina-based Hsq2000. About 10 to 35 million 58-bp. A legacy annotation of an organism "genemark predictions". What are my option to redo the annotations using the short read files I have.
Any tools, steps , suggestions, examples are really appreciated
Thank you!
I have a number of single-ended samples generated by Illumina-based Hsq2000. About 10 to 35 million 58-bp. A legacy annotation of an organism "genemark predictions". What are my option to redo the annotations using the short read files I have.
Any tools, steps , suggestions, examples are really appreciated
Thank you!
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