Shicheng Guo
Okay. I see. You have gave solution before. sed -e 's/\s,\+/\t/g' -e 's/,\+\s/\t/g' 16S1710LF01.txt | sed -e 's/;,\+/;/g' > 16S1710LF01.txt.sed.txt It works well. Thanks. Shicheng
Why not make a brief report of PileOMeth on bioinformatics? It will be very quick from submission to acceptation, I think.
Anway, We need a citation method, haha, please please please
Hi Nick, I download VCF files and try to find "likely pathogenic, Conflicting interpretations of pathogenicity" information, however, it looks ClinVar annotation is not existed in download VCF, right? Thanks....
Hi All, Looks like the issues still there. Anyone figure out the reason and the solution to solve the bugs? Thanks Shicheng
Thank you Patrick! it will be very helpful!! Shicheng
Sure. Thanks, Jonathan. I will double-check the above two situations you mentioned and share feedback with you. Shicheng
I am wondering can you share a bash script/demo script to show how eagle2 + minimac4 for phasing and imputation? Thanks.
Looks not so bad. I have 1262 phenotypes and, with single thread, `pheweb matrix` only takes 62880 seconds. I have a question: Is there any way to speed up `pheweb...
Do you think we should separate common variants and rare variants to different files and only perform rvtest to rare variants dataset, or we can take mixture dataset as input...