A tool set for short variant discovery in genetic sequence data.
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May 4, 2021 - C
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variant-calling
Here are 8 public repositories matching this topic...
De novo genome assembly and multisample variant calling
genomics variant-calling kmer cortex genome-analysis genome-assembly de-bruijn-graphs genome-graph contigs
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Mar 28, 2019 - C
This is the official development repository for BaseVar, which call variants for large-scale ultra low-pass (<1.0x) WGS data, especially for NIPT data
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Dec 17, 2024 - C
FPGA Acceleration for the LoFreq variant caller
bioinformatics fpga hls probability-distribution xilinx variant-calling bioinformatics-tool lofreq vitis-hls poisson-binomial-distribution counting-models
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Mar 10, 2024 - C
Multipurpose tool for targeted variant calling of genetic polymorphisms in Mycobacterium Tuberculosis
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Oct 24, 2023 - C
Variant calling format (vcf) file genomics pipeline for HPC and cloud
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Oct 12, 2017 - C
Stellenbosch University Variant Calling Pipeline
bioinformatics pipeline analysis python-script bioinformatics-pipeline variant-calling variant bioinformatics-analysis turbeculosis stellensbosch
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Feb 13, 2018 - C
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