Re: [Biopython] Calculating NS and S over a given sequence
"Riesgo Ferreiro, Pablo" <[email protected]> Wed, 6 Oct 2021 07:53:35 +0000
| Newsgroups | gmane.comp.python.bio.general |
|---|---|
| Message-ID | <[email protected]> |
Thanks Zheng, I will look into the details of the implementation. What I am in need is something like cal_n_s(ref_deq). I will check if it makes any sense to make this a public function. Best, Pablo ________________________________ From: Zheng Ruan <[email protected]> Sent: 30 September 2021 15:32:38 To: Riesgo Ferreiro, Pablo Cc: [email protected] Subject: Re: [Biopython] Calculating NS and S over a given sequence Hi Pablo, You can simply use cal_dn_ds(ref_seq, sample_seq) to achieve this. If you have multiple sample_seqs, you may iterate all of them. Internally, cal_dn_ds determines the N and S sites by averaging the N and S sites counted from both the ref_seq and sample seq. If you specify the NG86 method, it does the log transform as you show in the figure. Best, Zheng On Thu, Sep 30, 2021 at 5:24 AM Riesgo Ferreiro, Pablo <[email protected]<mailto:[email protected]>> wrote: Hi all, I am new to this mailing list. First of all many thanks for your work, I have happily used Biopython in several projects before. I have a need to compute the dN/dS ratio over a set of samples of the same species. I know this is not great 10.1371/journal.pgen.1000304, but still. I have found this feature in biopython calculating the dN/dS between sequences: https://biopython.org/docs/1.76/api/Bio.codonalign.codonseq.html#Bio.codonalign.codonseq.cal_dn_ds, but this does not cover my needs. What I need is to compute dN/dS based on the count of mutations over a set of samples as explained at https://bioinformatics.cvr.ac.uk/calculating-dnds-for-ngs-datasets/ [cid:7c03806e-bbb0-47b1-9c49-3c53e33af83e] N and S is dependent on the reference sequence and independent on the samples. N and S can be calculated on different genomic regions (eg: coding region, transcript, exon, domain, etc.). The simplest input for this tool would be a given ORF sequence and you would think of more complete things as a GFF file. It is a small thing, but unless anyone knows of an existing implementation, I think it may be useful to others. Do you think this would be a valuable contribution to biopython? Best wishes, Pablo Riesgo Ferreiro Computational Medicine TRON Translationale Onkologie an der Universitätsmedizin der Johannes Gutenberg-Universität Mainz gemeinnützige GmbH _______________________________________________ Biopython mailing list - [email protected]<mailto:[email protected]> https://mailman.open-bio.org/mailman/listinfo/biopython _______________________________________________ Biopython mailing list - [email protected] https://mailman.open-bio.org/mailman/listinfo/biopython
Screenshot from 2021-09-30 09-55-58.png
(image/png, 98 KB) - not displayed