Hello, I would like to know how I can find the position of a variant splicing on coding sequence. I'm using Aloft but if there is another solution I will take it.
Thank you.
I'm planning an experiment where I'll be over-expressing a certain gene in stem cell derived neurons (iPSC -> iN). For the over-expression, I would like …
Hello, I'm learning how to use PennCNV-Seq (pipeline for variant calling). I've already installed the dependencies (bedtools and pennCNV). I have to execute the command …
Hello!! I'm trying to get the coding sequences from several reference-genome assemblies. The reference-genome assemblies were obtained wit: GATK, samtools mpileup, bcftools, vcfutils.pl and seqtk. …