Open ksw9 opened 3 years ago
Hello, this is a useful feature. Thank you for suggesting it.
Fantastic, thank you Karthik! Is there a best way to stay updated about this? All the best, Katie
Dear Karthik, I hope you are doing well. I was hoping to follow-up to see if you plan to implement this? Thanks again!
Hey @ksw9 , sorry about the HUGE delay. I was busy with other epi projects and my thesis defense. I will try to get at this issue this month.
Hi Karthik, Thanks for getting back and for all of your work on iVar and genomic epi! Good luck with your defense, it will be incredible. All the best, Katie
From: Karthik @.> Date: Tuesday, June 8, 2021 at 3:49 PM To: andersen-lab/ivar @.> Cc: Katharine Walter @.>, Mention @.> Subject: Re: [andersen-lab/ivar] ivar variants: Output invariant sites (#84)
Hey @ksw9https://github.com/ksw9 , sorry about the HUGE delay. I was busy with other epi projects and my thesis defense. I will try to get at this issue this month.
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Hi, Thank you for your all of your work on this! I'm wondering if it is currently possible or would be possible to have an option to output invariant sites in the output VCF along with variant sites? It would be great to have depth of coverage and other annotations available for sites without an intrahost variant called, so that we could distinguish between "no-call" and reference allele genotypes, similar to options available in GATK.
Thank you in advance!