The SeqSQC is designed to identify problematic samples in NGS data, including samples with gender mismatch, contamination, cryptic relatedness, and population outlier.
|Author||Qian Liu [aut, cre]|
|Bioconductor views||Experiment Data Genome Homo_sapiens_Data Project1000genomes Sequencing Data|
|Maintainer||Qian Liu <[email protected]>|
|Package repository||View on Bioconductor|
Install the latest version of this package by entering the following in R:
Any scripts or data that you put into this service are public.
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.