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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Updated
May 28, 2026 - C++
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non-invasive-prenatal-test
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NIPT-human-genetics is a semi-automated workflow designed for the analysis of large-scale ultra-low-pass non-invasive prenatal test (NIPT) sequencing data in human genetic studies.
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Updated
May 30, 2026 - Shell
This is the official development repository for BaseVar, which call variants for large-scale ultra low-depth(<1.0x) WGS data, especially for NIPT data and ancient DNA
bioinformatics variant-calling cfdna low-coverage-sequencing nipt basevar non-invasive-prenatal-test
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Updated
Jul 4, 2026 - C++
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