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Can I use jcvi to plot the MCSCanX #244
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The default filtering criteria (BLAST filters to remove weak and tandem duplicates) are different between MCScanX and jcvi version. The default synteny block threshold is also different. That's why the numbers are different. However, both should be fine to use as long as you keep track of the parameters that were used. To plot MCscan results, you need to convert the MCScanX output to Haibao |
Could you please show in code how to convert the MCScanX output (.collinearity) to .anchors format? |
Sorry for the late response but you could try: python -m jcvi.compara.synteny fromaligns mc.collinearity Let me know if this doesn't work and also send me a small file for testing. |
@tanghaibao |
Hi @tanghaibao, I wish to play with my macrosynteny plots in SynVisio. Many thanks, really liking the software so far |
Unfortunately, we don't yet have a conversion script as you said at this point. If you do figure out how to do it, please consider contributing this. I think other ppl have asked about this in the past. Haibao |
Hi mrmrwinter, |
I can not plot the synteny graph. The script gave me an error when I try to do it. It said that the chromosomes are empty. Could it be a problem with the seqid or layout files? |
Hi ,Mr Tang
I use MCSCanX to find collinearity blocks and found about 1000 blocks between two species ,However When I use the jcvi only 523 blocks in the Jcvi. My question is Can I use the MCScanX results to plot the Synteny between the two species ?
Thank you
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