Hi everyone, I’m working with EstiAge and need help finding or building the gnomAD_file and hapmap_file for Chromosome 16 in GRCh38. Does anyone know where …
Hello! This article https://gatk.broadinstitute.org/hc/en-us/articles/360035535932-Germline-short-variant-discovery-SNPs-Indels- says i should use HaplotypeCaller in GVCF mode and GenotypeGVCFs then, and this article https://gatk.broadinstitute.org/hc/en-us/articles/360035531192-RNAseq-short-variant-discovery-SNPs-Indels- advises to use HaplotypeCaller without GenotypeGVCFs. …
how can i get the know sites of the rice for BaseRecalibrator? samtools(mpileup)+bcftools? or gatk Haplotypecaller? finally i want to get the credible snps and …
Following are my DNAseq pipeline steps keeping GATKBestPrac in mind: Step1-Quality check of raw data (fastqc) Step2-Alignment with reference genome(bwa) Step3-SAM to BAM conversion and …
<p>I have generated sequence variants (SNPs/INDELs) by NGS resequencing and would like to display them on the UCSC browser (I have resequenced against a UCSC …
After HaplotypeCaller, you can use gatk SelectVariants to extract snps or indels from vcf file (link to command)