Hello, I have tried followed procedure for polygenic risk score analysis with whole genome sequencing data and just want to be sure that there are …

Hi! Is there some open-access database, where I could get vcf files for some healthy people (preferably with EU ancestry and with hs27 reference)? I …

These are purely statistical/ analysis/ theoretical method questions. I am now conducting a gene/ variant association study between a gene(G) and disease as well as …

Hi, I don't know where and in which form to ask this question, I try here... We know that some very rare variants may cause …

I do have a long list of variants and would like to know which software or database is considered standard for clinical interpretation, particularly whether …

Hi! I am looking for ngs data with low sequence quality, but I don't know where to look for such data.I heard something about GATC …

Hi, I have 5 set of vcf files aligned using BWA and variants are called using GATK. I'm interested to find for common SNPs that …

I'm accessing diferent databases to collect data for different variants found in a human sequence. One of the databases that I want to use is …

Hello all, I am analyzing the variant call analysis from my** identical twins**. (they are confirmed as having a same disease-causing mutation, which was a …

Hi I used blast2go in order to find similar genes to my transcriptome profile, How can I identify significant kegg pathways for these genes(Profile)? And, …