There are multiple steps to call genotype, which described in our user manual.
Here is the running time for each step in our test data set(about 1250M single end reads) in our cluster (12 Intel CPU cores, 16G memory):
1. Indel realign step:
about 12 hours
2. Base quality recalibration step:
about 24 hours
3. Bisulfite genotyping step:
By default output mode (cpg.vcf and snp.vcf):
35 hours
4. VCF postprocess to filter fake SNP, convert to bed format:
about 2 hours
Notes: Time cost is not strictly linear correlated with the reads number. Indel realign step is exponential increase with reads number. While Bisulfite genotyping step would be more correlated with interval size to go through and output mode selection, 200M reads in the whole genome may still cost 24 hours, but 100M reads in chr1 may only take less than 8 hours.
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