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Recent Replies
Answer: How to visualize Multiple Sequence Alignment with python ?
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Can't think of a particularly good alignment viewer in python.
If you are more interested in result rather than doing it in python, ther…
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> Wouldn't a gene that isn't an ABC superfamily member from some distant species suffice as an outgroup candidate here?
Most definitely no…
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with that definition I would suspect that all of your sequences are "dependent", I would expect every functional DNA/RNA region to capture …
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Thanks!
As for the blast option- (1) so do you suggest to just blast the contig against a db of viral RNAs? and (2) is there a comprehensiv…
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#!/usr/bin/env python3
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Thanks for your reply. Yes, I think I could have explained my problem much better, but rather than change my original post, I will add some…
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Here's a little `python` function you can work off of:
def count_quer_at_pos_in_seq(seqs, quer = "A"):
#Initialize a list…
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Thank for the fast reponse. The ABC family is not the best example for this question indeed.
The objective of my work is to find genes resp…
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1. Blast directly
2. [IDSeq][1], can get viral contigs and their annotation directly.
[IDSeq : An open-source cloud-based pipeline and…
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Hi, It is not a norm but it is a good practice to post an attempted resolution first and then other members try to correct it or suggest an…
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Aye to the rushed analyses and the last-minute documentation. Horrible, but somehow it happens all the time.
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Reinventing the wheel. Like, all the time. Why use clusterProfiler with an up-to-date GO-annotation, when you can just write your own clien…
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By "pooled" data, do you mean data from tissue-specific bulk-RNAseq?
Or did you pool single cell (SC) RNAseq-libraries?
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What exactly do you mean by "pooled" data?
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I made a tutorial last year for University students on this topic https://www.loom.com/share/a55c1dedb8e64e7cac47f6595b751de7. Let me know …
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