## User: gtechbio

gtechbio0
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#### Posts by gtechbio

<prev • 11 results • page 1 of 2 • next >
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... Thanks for elaborating!Now it makes sense for me. And I guess for human data (i.e. patients or any "case-control" study) this "individualized" approach would matter compared to mine. In my case though I analyze yeasts (they are quite homogenous within the culture), so I can in principle assume that ...
written 11 weeks ago by gtechbio0
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... Hi Michael, I am sorry for ignorance, but still I don't understand why my example wouldn't work properly: I specify in design formula that there are two conditions (basically parents), and I control for library size and gene length. So basically it will compare condition 1 vs condition 2, and will s ...
written 11 weeks ago by gtechbio0
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... Dear Michael, Regarding normalization, so thanks a lot, I will try running the code like that. Regarding the count table, so for example SC1 and SU1 are from the same library (as other samples with the same numbers), and I thought my design will compare alt to ref, like you have mentioned, won't i ...
written 11 weeks ago by gtechbio0
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... Dear Michael, I was wondering if in DESeq2 it is possible to simultaneously set size factors and control for gene length (like you have suggested in your post)? Thanks in advance ...
written 12 weeks ago by gtechbio0
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... Hi Michael, Thanks for reply. Just to make sure I do everything in order: My count_table looks like SC1 SC2 SC3 SU1 SU2 SU3 YBR177C_Sbay_4.429 2711 3397 3765 1246 2156 3287 YIL140W_Sbay_9.48 178 111 204 109 271 250 Y ...
written 12 weeks ago by gtechbio0
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... Hi, I want to use DESeq2 for assessing allele-specific expression. I will compare gene-level allelic counts of a yeast hybrid (basically comparing counts of orthologous genes of parentals of this hybrid). I'm aware of this tutorial http://rstudio-pubs-static.s3.amazonaws.com/275642_e9d578fe1f7a404aa ...
written 3 months ago by gtechbio0 • updated 3 months ago by Michael Love18k
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... Thanks for your time Michael and sorry for coming back to you late. As far as I understand, with LRT the software will find a gene which became differentially expressed at any time point. In this case we assume, that if gene is changing its expression, this change is always towards one direction - ...
written 8 months ago by gtechbio0
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... Hi Michael, thank you for your reply. Could you also please point out what is the conceptual difference between this approach and LRT-based time-course analysis, and whether any of those has advantages or disadvantages over another? And one more question regarding shrinkage (sorry if a silly one): ...
written 8 months ago by gtechbio0
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... Hi All, This is to make sure I do a correct thing (which might be actually wrong). I have a time series experiment: 0 time point - yeast is growing alone (control), 3,12,24h time point - yeast is growing on human cells, and 24h (control) - yeast is growing alone. I need to do a time-series DE anal ...
written 8 months ago by gtechbio0 • updated 8 months ago by Michael Love18k
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Comment: C: DESeq2 for ASE
... Hi Michael, Thanks for reply! As far as I understand, in your example there are two conditions, while my case actually the are no conditions - I just need to compare ref and alt counts. So condition in my formula represents the alleles in fact. In this situation do you think the above analysis is ...
written 9 months ago by gtechbio0

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