gatk | Official code repository for GATK versions | Genomics library
kandi X-RAY | gatk Summary
kandi X-RAY | gatk Summary
This repository contains the next generation of the Genome Analysis Toolkit (GATK). The contents of this repository are 100% open source and released under the Apache 2.0 license (see LICENSE.TXT). GATK4 aims to bring together well-established tools from the GATK and Picard codebases under a streamlined framework, and to enable selected tools to be run in a massively parallel way on local clusters or in the cloud using Apache Spark. It also contains many newly developed tools not present in earlier releases of the toolkit.
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Top functions reviewed by kandi - BETA
- Call a region .
- Creates a Sequence comparator for the given variant .
- Preprocess the input panel
- Find hmm in local format .
- Run the DEST function .
- Call Hatch results .
- Simple merge method .
- Find the best haplotypes .
- Calculate Geneotypes .
- Validates the plugin arguments .
gatk Key Features
gatk Examples and Code Snippets
Community Discussions
Trending Discussions on gatk
QUESTION
The 1st column of the subjects_153_ped
dataframe corresponds to the Database_ID
column of the ann
dataframe.
The 5th column of the subjects_153_ped
dataframe corresponds to the sex
column of the ann
dataframe.
The 6th column of the subjects_153_ped
dataframecorresponds to the
Profilecolumn of the
ann` dataframe.
Here, I pheno
is the subset where:
(1) 1st column (FID): Database_ID
column (from ann
clinical table)
(2) 2nd column (IID): 1 (hardcoded)
(3) 3rd column (PAT): 1 (hardcoded)
(4) 4th column (MAT): 1 (hardcoded)
(5) 5th column (SEX): sex
column (from ann
clinical table)
(6) 6th column (PHENOTYPE): Profile
column (from ann
clinical table)
(7) Column 7 onwards are info from the original subjects_153_ped
dataframe
Desired file formatting: PED file format https://plink.readthedocs.io/en/latest/plink_fmt/ https://gatk.broadinstitute.org/hc/en-us/articles/360035531972-PED-Pedigree-format
Expected output
FID IID PAT MAT SEX PHENOTYPE ALL OTHER COLUMNS AC10 1 1 1 M Schiz. ALL OTHER COLUMNS AC11 1 1 1 M Schiz. ALL OTHER COLUMNS AC12 1 1 1 M Schiz. ALL OTHER COLUMNS AC13 1 1 1 F BP ALL OTHER COLUMNS ...ANSWER
Answered 2022-Mar-20 at 15:32Perhaps this helps - select and create new columns in ann
with transmute
, and left_join
with the 'subjects_153_ped' using the 'FID' and 'V1' as by
QUESTION
I've been struggling to identify why a nextflow (v20.10.00) process is not using all the items in a channel. I want the process to run for each sample bam file (10 in total) and for each chromosome (3 in total).
Here is the creation of the channels and the process:
...ANSWER
Answered 2022-Mar-05 at 15:20Issues like this almost always involve the use of multiple input channels:
When two or more channels are declared as process inputs, the process stops until there’s a complete input configuration ie. it receives an input value from all the channels declared as input.
Your initial assessment was correct. However, the reason only three processes were run (i.e. one sample for each of the three chromosomes), is because this line (probably) returned a list (i.e. a java LinkedList) containing a single element, and lists behave like queue channels:
QUESTION
I have a folder containing paired files with names that look like this:
...ANSWER
Answered 2022-Mar-03 at 17:38I'm trying to fully understand what you want to do here.
If you want to extract just the first two parts, this should do:
QUESTION
I can't seem to get GATK to recognise the number of available threads. I am running GATK (4.2.4.1) in a conda environment which is part of a nextflow (v20.10.0) pipeline I'm writing. For whatever reason, I cannot get GATK to see there is more than one thread. I've tried different node types, increasing and decreasing the number of cpus available, providing java arguments such as -XX:ActiveProcessorCount=16
, using taskset
, but it always just detects 1.
Here is the command from the .command.sh
:
ANSWER
Answered 2022-Feb-15 at 17:02In case anyone else has the same problem, it turned out I had to configure the submission as an MPI job.
So on the HPC I use, here is the nextflow process:
QUESTION
Sorry if this is gonna be probably a duplication of other questions, but I couldn't figure to debug what's going on in my case. Got a dataframe like this:
...ANSWER
Answered 2022-Feb-15 at 11:15The parameters are stored in a dataframe, and there is a handy utility for working with tabulated parameters, Paramspace
. Below is a rough take on your specific case, but it will need some adjustments for command syntax and paths.
First step is to reshape the data for easier workflow:
QUESTION
The output of my first command line "bcftools query -l {input.invcf} | head -n 1"
prints the name of the first individual of vcf file (i.e. IND1
). I want to use that output in selectvariants GATK
in -sn IND1
option. How is it possible to integrate the 1st comamnd line in snakemake in order to use it's output in the next one?
ANSWER
Answered 2022-Feb-04 at 12:52I think I found a solution:
QUESTION
In the second rule I would like to select from the vcf file containing bob, clara and tim, only the first genotype of dictionary (i.e. bob) in roder to get as output in the second rule bob.dn.vcf
. Is this possible in snakemake
?
ANSWER
Answered 2022-Feb-03 at 13:32There are at least two options:
- explicitly specify output:
QUESTION
I'm trying to use recalibrate my vcf using gatk VariantRecalibrator, but keep getting an error "Illegal argument value: Positional arguments were provided". But I don't know what this means, or how to correct it!
Here's my call:
...ANSWER
Answered 2022-Jan-06 at 17:12The error message in this case is confusing. The --resource
arguments aren't formatted correctly and extra whitespace is causing it to interpret the following arguments as positional arguments.
The problem is that --resource
blocks should have the meta information attached to the argument name instead of separated with a space.
i.e.
--resource:hapmap filename
instead of --resource hapmap: filename
The GATK Forum is a good place to get answers to questions like this.
QUESTION
I have written a rule for CombineGVCFs in gatk4. The rule is as follow
...ANSWER
Answered 2021-Sep-16 at 17:18Found out the problem. Turns out I can write a lambda function as follows
QUESTION
I am using snakemake to describe the GATK pipeline. I need to run the following command:
...ANSWER
Answered 2021-Jun-02 at 08:13You could do this:
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Install gatk
You can use gatk like any standard Java library. Please include the the jar files in your classpath. You can also use any IDE and you can run and debug the gatk component as you would do with any other Java program. Best practice is to use a build tool that supports dependency management such as Maven or Gradle. For Maven installation, please refer maven.apache.org. For Gradle installation, please refer gradle.org .
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