This page documents how to perform variant calling from low-coverage sequencing data using glfmultiples and thunder. The pipeline was originally developed by Yun Li for the 1000 Genomes Low Coverage Pilot Project.
- 1 Input Data
- 2 How to Run
- 3 Important Filters
- 4 Questions and Comments?
If you do not have glf files, you can generate them from bam files (bam format also specified in glf format bam format) using the following command line:
samtools pileup -g -T 1 -f ref.fa my.bam > my.glf
Note: you will need the reference fasta file ref.fa to create glf file from bam file.
How to Run
(step 1) Site promotion using software glfMultiples GPT_Freq
GPT_Freq -b my.out -p 0.9 --minDepth 10 --maxDepth 1000 *.glf
(step 2) Genotype/haplotype calling using thunder thunder_glf_freq
thunder_glf_freq --shotgun my.out.$chr -r 100 --states 200 --dosage --phase --interim 25 -o my.final.out
(1) The program thunder used in step 2 is an extension of MaCH, the genotype imputation software we have previously developed. For details regarding the shared options, please check out MaCH website and MaCH wiki.
(2) Check out example files and command lines under examples/thunder/ in the thunder package thunder_glf_freq.
We have found that the following filters are helpful.
total depth filter
For the 1000 Genomes Project (average depth per individual ~4X), we have found it useful to exclude sites with average total depth per individual < 0.5X or > 10X.
We recommend the filter of >50% individuals with coverage.
flanking sequence filter
We recommend excluding sites with >0.1% flanking 10-mer frequency among candidate sites.
The rationale is ....
We recommend distance to known indels >= 5bp. A catalog of known indels can be found at [ indel catalog].
site promotion filter
We recommend setting parameter -p at least >= 0.9 in step 1 (running glfMultiples).
Questions and Comments?
Email Yun Li.