More posts like this
-
How to extract and analyze variant sequences from gnomAD v4 exome VCF
written by Rohan •I am working on a pharmacogenomics study focusing on the GPCR gene family and analyzing variant sequences in ~700,000 individuals from the [gnomAD v4 exome …
-
What is chrom and position values in Wuhan-Hu-1 genome data
written by Nemo •Hi, I have variants from covid samples using gatk and haplotype caller. In the resulted table, for each sample and variant there is two columns …
-
GnomAD subset vcf files
written by kanika.151Hello All, Do you know how to extract variants related to a specific population from the GnomAD exome vcf file? In ExAC, one can find …
-
gnomAD AF = 0 vs gnomAD AF = NA (gnomad V2)
written by jon.klonowskiHello, I was looking at VEP annotated gnomad AF (gnomad V2, exomic, since I am analyzing exomes) and noticed that there was a class that …
-
Does GNOMAD use all LOFTEE LoF filters?
written by brismiller •Hi all, I have some lof variants and I want to know if they have already been detected in GNOMAD (I am essentially curious if …
-
gnomAD: query utilitites
written by bsmith030465Hi, I wanted to query the gnomAD database without having to download and configure the entire data. Is there a way gnomAD provides an API …
-
Extract allele count from gnomAD using R
written by Nicolas RosewickHi, Is there a way to extract the allele count for each population of a specific variant using R (oar maybe through a REST API …
-
Forum: Create a File format to store Variant
written by sachaHi, BED format or VCF format are not well designed to store [hgvs][1] notation and metadatas of a variant. I would like to have a …
-
remove a percent of reads from a BAM file
written by sachaI would like to remove x% of reads from a BAM file at a specific region . For instance : remove 50% of reads in …
-
bcftools extract data
written by sachaWithout awk, only with bcftools, is there a way to view selected data from a vcf file? For example, show only Depth value, something like: …