The SeqSQC is designed to identify problematic samples in NGS data, including samples with gender mismatch, contamination, cryptic relatedness, and population outlier.
Package details |
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Bioconductor views | Experiment Data Genome Homo_sapiens_Data Project1000genomes Sequencing Data |
Maintainer | |
License | GPL-3 |
Version | 1.9.1 |
URL | https://github.com/Liubuntu/SeqSQC |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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