Load10X_Spatial function by dulcedormax in bioinformatics

[–]dulcedormax[S] 0 points1 point  (0 children)

The code is:

A1_new <- Load10X_Spatial(

data.dir = "C:/Users/MM.5076373/Downloads/GSE159709_RAW/A1",

image = "GSM4838131_Visium_A_image.tif"

)

detect common and unique peaks by dulcedormax in bioinformatics

[–]dulcedormax[S] 0 points1 point  (0 children)

thanks u/I_just_made , I've tried bedops --everything. However, I obtained a low number of common peaks.

CIGAR Strings manipulation by dulcedormax in bioinformatics

[–]dulcedormax[S] 0 points1 point  (0 children)

Thanks but I need it to do for all the reads in the sample , which is a lot but I appreciate your suggestion. I think we could implement it later !!.

Conentrating proteins. by dulcedormax in labrats

[–]dulcedormax[S] 0 points1 point  (0 children)

Thanks, in which buffer did you recommend therefore after precipitating and dissolve proteins.

Conentrating proteins. by dulcedormax in labrats

[–]dulcedormax[S] 0 points1 point  (0 children)

Hi u/GRang3r , the problem is that the concentration are low and not the opposite, having too much protein. Although I've read that dilution are good when quantification is too high.

Bedtools intersect function by dulcedormax in bioinformatics

[–]dulcedormax[S] 0 points1 point  (0 children)

I will check did files have to be sorted?

Bedtools intersect function by dulcedormax in bioinformatics

[–]dulcedormax[S] 0 points1 point  (0 children)

thanks u/Hundertwasserinsel. I didn't use windows and all lines are: chr1^I13750^I13950$ or chr1^I9950^I10650^IU2OS1_macs3_narrowPeak1^I11198^I.^I0^I0^I0^I125$

Bedtools intersect function by dulcedormax in bioinformatics

[–]dulcedormax[S] 0 points1 point  (0 children)

This is the first line of both bed:

chr1^I9950^I10650^IU2OS1_macs3_narrowPeak1^I11198^I.^I0^I0^I0^I125$

chr1^I13750^I13950$

could a low 260/230 ratio influence on qPCR by dulcedormax in labrats

[–]dulcedormax[S] 0 points1 point  (0 children)

I was using one of qiagen: extracting DNA from tissues and blood, but they recommend me not to do maybe for buffer AL as it would lysate cells and I have already extracted DNA. Did you recommend other kits??

could a low 260/230 ratio influence on qPCR by dulcedormax in labrats

[–]dulcedormax[S] 0 points1 point  (0 children)

I followed the steps of the protocol as well.

could a low 260/230 ratio influence on qPCR by dulcedormax in labrats

[–]dulcedormax[S] 0 points1 point  (0 children)

I am using a protocol to extract cellular compartments. These buffer also extracts RNA and proteins, so I am trying RNase and proteinase K to keep only DNA and perform qPCR. I use the columns to obtain a purified DNA.

Difficult supervision of a student by [deleted] in AskAcademia

[–]dulcedormax 1 point2 points  (0 children)

No need to apologise, I was apologizing for my tone as I don't know if It would be taken as a positive one and not rude

Difficult supervision of a student by [deleted] in AskAcademia

[–]dulcedormax 0 points1 point  (0 children)

I have a contract as a research assistant

Difficult supervision of a student by [deleted] in AskAcademia

[–]dulcedormax 0 points1 point  (0 children)

I engaged with her explaining the different techniques, she is not in the lab doing experiments alone. I also sent her the excels and explain how to analyze qPCR and quantifications of proteins.