Quantcast
Channel: Recent Discussions — GATK-Forum
Browsing all 12345 articles
Browse latest View live

VariantRecalibrator: ERROR MESSAGE: NaN LOD value assigned.

I have some gVCF files, and I need to call variants from them. I am able to use HaplotypeCaller successfully, but VariantRecalibrator is giving me error. java -jar /storage/s1saini/GenomeAnalysisTK.jar...

View Article


Picard vcf filtering

Hi, I use Picard to filter a vcf file. It seems not to function propely. I am filtering on read depth using MIN_DP=50 but I still see a lot of genotypes in the resulting file with lower coverage than...

View Article


Run GATK on files stored in AWS S3?

Hi, Same as title: Is it possible to run GATK on files stored on S3?

View Article

VCF input and BaseRecalibrator error

I'm trying to run BaseRecalibrator with GATK4-Alpha. I'm using --knownSites to input a vcf file as follows: java -Xmx80G -jar $GATK BaseRecalibrator \ -R reference.fa \ -I ${SAMPLE}_dedup.bam \...

View Article

Variant detection in RNAseq: when to merge samples

Hi, I have followed the recommendations for my RNAseq variant search as outlined here: http://gatkforums.broadinstitute.org/gatk/discussion/4067/best-practices-for-variant-discovery-in-rnaseq Since I...

View Article


Mutect is not working

Dear Cancer team, I installed mvn, gatk-protected, and mutect. (https://github.com/broadinstitute/mutect) After that, I came upon the following error message: ERROR...

View Article

VQSLOD score different for Full and split (by chromosome) BAM file

Dear all, I am trying to generate VCF using full and split (by chromosome) BAM files by GATK but after successful completion, there are difference in the VQSLOD score: For full : VQSLOD=-6.339e-01 For...

View Article

Image may be NSFW.
Clik here to view.

Genotype Refinement workflow

Overview This document describes the purpose and general principles of the Genotype Refinement workflow. For the mathematical details of the methods involved, please see the Genotype Refinement math...

View Article


Empty ContEst Output

Hello, I have some truseq cancer panel amplicon data and I am in process of calling Somatic variants in Tumor samples with MuTect. By using the default fraction_contamination, I am not getting any...

View Article


variant calling with biological replicates

I am new to use GATK pipeline for SNP calling. I am currently working on four different populations (RNASEq data) with 6 clones. Each clone has 3 biological replicates. How do I combine the variant...

View Article

I get very different MQ values when using GVCF vs BP_RESOLUTION

Hello! I had a question about the difference between using HaplotypeCaller's --emitRefConfidence GVCF vs BP_RESOLUTION. Maybe the answer is obvious or in the forum somewhere already but I couldn't spot...

View Article

Web-based Oncotator server

There is a web-based version of Oncotator which you can use for annotation without running anything on your own machine. However, please note that the web-based version is an older version, with fewer...

View Article

Advice for running GenotypeVCF and Recalibration on a thousand samples

Hi, I am working with a couple thousand gVCFs. I plan to run GenotypeGVCF and ApplyRecalibration on them in a joint fashion. I want to know how does GATK scale on these numbers, and is it even...

View Article


Posters on somatic analysis with GATK4 presented at AACR 2017

A few of us GATKers (among a flood of other Broadies) traveled to Washington, DC this week for the General Meeting of the American Association for Cancer Research (AACR). Here are PDF copies of the...

View Article

Anticipate "--fix_misencoded_quality_scores"

Hello everyone, I've created a full Variant Calling pipeline (on Galaxy). There is of course the IndelRealignment phase done by GATK. We all know now the solution of the "SAM/BAM file x appears to be...

View Article


Questions about DepthOfCoverage

This discussion was created from comments split from: Using DepthOfCoverage to find out how much sequence data you have.

View Article

Image may be NSFW.
Clik here to view.

Best Practices for Variant Discovery in RNAseq

This article is part of the Best Practices documentation. See http://www.broadinstitute.org/gatk/guide/best-practices for the full documentation set. This is our recommended workflow for calling...

View Article


How can I access the GSA public FTP server?

NOTE: This article will be deprecated in the near future as this information will be consolidated elsewhere. We make various files available for public download from the GSA FTP server, such as the...

View Article

How can I invoke read filters and their arguments?

Most GATK tools apply several read filters by default. You can look up exactly what are the defaults for each tool in their respective Technical Documentation pages. But sometimes you want to specify...

View Article

Purpose and operation of Read-backed Phasing

This document describes the underlying concepts of physical phasing as applied in the ReadBackedPhasing tool. For a complete, detailed argument reference, refer to the tool documentation page. Note...

View Article
Browsing all 12345 articles
Browse latest View live


<script src="https://jsc.adskeeper.com/r/s/rssing.com.1596347.js" async> </script>