GotCloud: Variant Calling Pipeline

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The Variant Calling Pipeline (previously called 'UMAKE') makes genotype calls from recalibrated BAM files. These genotype calls are output into VCF (Variant Call Format) files.

Running the GotCloud Variant Calling Pipeline

The variant calling pipeline (umake) is run using gotcloud snpcall and gotcloud ldrefine. gotcloud is found under gotcloud/.

Running the Automatic Test

The automatic test runs the variant calling pipeline on a small testset and checks the results against expected results validating that GotCloud is installed correctly.

• Run variant calling pipeline test:

gotcloud snpcall --test OUTPUT_DIR

where OUTPUT_DIR is the directory where you want to store the test results

If you see "Successfully ran the test case, congratulations!", then you are ready to align samples.

Overview of Variant Calling Pipeline Steps

Here is an overview of the Variant Calling Pipeline:

Input Data

• Aligned/Processed/Recalibrated BAM files
• Index file containing Sample IDs & BAM file names
• Reference files
• (Optional) Configuration file to override default options

BAM files

The BAM files need to be duplicate-marked and base-quality recalibrated in order to obtain high quality SNP calls. Generating these BAM files from original FASTQs is documented elsewhere as part of the Alignment Pipeline of gotCloud.

Index File

Each line of the index file represents each individual under the following format. Note that multiple BAMs per individual may be provided.

[SAMPLE_ID]    [COMMA SEPARATED POPULATION LABELS] [BAM_FILE1] [BAM_FILE2] ...

Columns:

1. sample id
2. comma separated population labels
3. BAM File 1 (preferable to have full paths to BAM files)
4. BAM File 2 (if applicable)

...

# BAM File N

Reference Files

The variant calling pipeline requires multiple reference files in order to work correctly.

• Reference Sequence in fasta format.
  • Configuration File Setting: REF = path/file.fa
• Indel VCF File Prefix
  • Configuration File Setting: INDEL_PREFIX = path/indels.sites.hg19
  • path/ contains indels.sites.hg19.chr20.vcf for each chromosome being processed
• DBSNP File Prefix
  • Configuration File Setting: DBSNP_PREFIX = path/dbsnp_135_b37.rod
  • path/ contains dbsnp_135_b37.rod.chr20.map for each chromosome being processed
• HapMap3 polymorphic site prefix
  • Configuration File Setting: HM3_PREFIX = path/hapmap3.qc.poly
  • path/ contains hapmap3.qc.poly.chr20.bim & hapmap3.qc.poly.chr20.frq for each chromosome being processed

A set of reference files can be downloaded from: [| FTP Download of Full Resource Files]

Configuration File Example Reference Settings:

REF = path/file.fa
INDEL_PREFIX = path/indels.sites.hg19
DBSNP_PREFIX = path/dbsnp_135_b37.rod
HM3_PREFIX = path/hapmap3.qc.poly

Configuration File

Configuration file contains the run-time options including the software binaries and command line arguments. A default configuration file is automatically loaded. Users must specify their own configuration file specifying just the values different than the defaults.

Comments begin with a #

Format: KEY = value

Where KEY is the item being set and value is its new value

Required User Config Files Settings

The following Config File Settings must be specified by the user:

• CHRS = space separated list of chromosomes you want
• BAM_INDEX = path to the Index File of BAMs

Required on Command-Line or in Config File

The following Command-Line or Config File Settings must be specified by the user:

• --outdir/OUT_DIR= path to desired output directory

Targeted/Exome Sequencing Settings

If you are running Targeted/Exome Sequencing, the user should specify:

• Write loci file when performing pileup
  • WRITE_TARGET_LOCI = TRUE
• Specify the output sub-directory to store target information, for example: targetDir
  • Should not be a full path as this will co under the OUT_DIR directory.
  • TARGET_DIR = targetDir

If all individuals have the same target:

• Specify the single bed file, for example: target.bed
  • UNIFORM_TARGET_BED = target.bed

If not all individuals have the same target:

• Specify the file containing the sample id -> bed map, for example: targetMap.txt
  • MULTIPLE_TARGET_MAP = targetMap.txt
    • Each line of the file contains [SM_ID] [TARGET_BED]

Optional Settings:

• Extend the target region by a given number of bases, for example: 50
  • OFFSET_OFF_TARGET = 50

Configure Reference Files

See Reference Files for information on how to specify the reference files.

Chromosome X Calling

• PED_INDEX = pedfile.ped

Running

Running variant calling is straightforward:

gotcloud snpcall --conf vc.conf --numjobs 2
gotcloud ldrefine --conf vc.conf --numjobs 2

Replace vc.conf with the approprate path/name of the user's configuration file.

If OUT_DIR is not defined in the configuration file, add --outdir followed by the path to the user's desired output directory.

Update the value following --numjobs to the appropriate number of jobs to be run in parallel.

Running on a Cluster

To run on the Cluster, the following settings need to be added to the configuration file:

TODO: COMING SOON

SLEEP_MULT =     20
REMOTE_PREFIX =  # REMOTE_PREFIX : Set if cluster node see the directory differently (e.g. /net/mymachine/[original-dir])

Results

If there is a failure, you should see a message like:

make: *** [...] Error 1

Where ... is filled in with other text indicating what step failed.

On SNP Call success, you should see the following output sub-directories under your output directory:

• glfs with a bams & samples subdirectory
• pvcfs with a subdirectory per chromosome and then per region
• split with a subdirectory per chromosome
• vcfs with a subdirectory per chromosome
• (optionally your target directory)

Under the vcf/chrXX directory, there should be:

• chrXX.filtered.sites.vcf
• chrXX.filtered.sites.vcf.log
• chrXX.filtered.sites.vcf.summary
• chrXX.filtered.vcf.gz
• chrXX.filtered.vcf.gz.OK
• chrXX.filtered.vcf.gz.tbi
• chrXX.merged.sites.vcf
• chrXX.merged.stats.vcf
• chrXX.merged.vcf
• chrXX.merged.vcf.OK

The .merged.vcf is the merged together versions of the separate regions in the same chromosome.

The filtered is the merged.vcf after it has been run through filters and is marked with PASS/FAIL.

Under the split/chrXX directory, there should be:

• chrXX.filtered.PASS.split.[N].vcf.gz
• chrXX.filtered.PASS.split.err
• chrXX.filtered.PASS.split.vcflist
• chrXX.filtered.PASS.gz
• subset.OK