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Recent Replies
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That's great. I will test it and let you know how it goes. Thank you.
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I tried running BLAT, but the output looks like this. Seems like none of the sequences were mapped/aligned
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You could try and look up a snapshot of the page(s) - https://web.archive.org/
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you could run blast or any other aligner to get the coordinate(s) of your fasta on a reference genome.
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If it cans help,
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I am not sure whether it will speedup the conversion but you can give it a try.
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The timing for your question is excellent. The fix was released yesterday.
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Well-noted however just wondering what you me by GFF being shorter. Thank you![See the screeshot snap of the gff file][1]
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I know illumina will only give me high-quality contigs.
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Hi, Thank you for a detailed responce.
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Here's a more neat version of the plot generated while writing my dissertation:
![enter image description here][1]
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what a pity...
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Yes, I can. But there are only two factors that affect my data PCA distribution: groups and donor. And the rest is regarded as residual.
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