Extracting Modifier/gene from .vcf file
Hello,
I cannot figure out to which modifier/gene corresponds the last array of values(i.e GT:AD:AF....).
Thanks!
vcf
gene
vep
modifier
• 1,267 views
•
link
updated
by
Pierre Lindenbaum
•
written
by
Ihor •
0 answers
No answers yet.
Log in to answer this question.
More posts like this
-
Asking for source of the figure
written by 张炘荣 •Could anyone help me find the source of this figure?![enter image description here][1] [1]: /media/images/2a828f52-460e-401f-bda4-fe56b198 Thanks a lot.
-
Tutorial: Step by step tutorial to replicate a genomics figure
written by Ming Tommy TangHello Bioinformatics lovers, I spent the holiday writing this tutorial https://crazyhottommy.github.io/reproduce_genomics_paper_figures/ to replicate this figure ![enter image description here][1] Happy Learning! Tommy [1]: /media/images/b9833ba7-6236-434a-868b-444ec473
-
Understanding IGV
written by zizigoluHi I have targeted sequencing (WGS) I have uploaded bam and vcf file for sample; From these screenshot which one shows/support this mutation ![enter image …
-
Cannot install bwa-mem2 via conda
written by jsmith120f •![enter image description here][1] ![enter image description here][2] [1]: /media/images/bdc78d9c-8f67-4be7-a5cc-69d949db [2]: /media/images/4d25a116-4670-4cf2-999b-28550bb9 I cannot seem to figure out what is going on, have also tried …
-
how to costum the color palette for ggplot2
written by Qianjiang(QJ) Hu •Hi, I use the following code to get the heatmap (figureA): **My code:** ![enter image description here][1] **Figure A** ![enter image description here][2] However, I …
-
How I know the genome assembly quality by the low coverage Pacbio data ?
written by wdpang •Hi, I have finished the assembly genome, and i have a low average Pacbio data. I want to estimate the quality of the result. So, …
-
Tools to plot gene arrow diagram
written by m.koohi.mHi, I am wondering with which tool I can plot the gene clusters like BGCs. Like figure below: ![enter image description here][1] Or like Fig …
-
How tp Extract SNPs values
written by Raju •Hello I have two files MaleSNPsList.txt (in which I have a list of SNPs) and MaleSNPsValues.ped (in which I have SNPs values extracted for SNPs). …
-
Is the current R version (4.1.2) are not suitable for the packages related with TCGA
written by nonaddldy •I cannot install series of packages related with TCGA, no matter through BiocManager::install or install.packages ![enter image description here][1] ![enter image description here][2] ![enter image …
-
Salmon Script Troubleshooting for RNA Seq Data
written by makylakb •Hello! I am working on a Slurm sbatch bash script to perform RNAseq analysis with Salmon in an HPC environment. I keep receiving the error …
your question is not clear to me. What are those reds marks ? The variant is REF=T/ALT=G and the sample is heterozygous T/G.
Oh, just ignore the red marks(it is for my convenience). I need to extract "MODIFIER" from each record, but I do not know which one corresponds to VAF. I see that there are multiple "MODIFIER", "ENSG", "ENST", etc but which one is the right one? I got this VEP but do not fully understand why we have multiple "MODIFIER" for each CHROM POS(i.e 13813 in this case).
https://en.wikipedia.org/wiki/Alternative_splicing