bni1/bohan_dev repository overview

Descriptions from: https://github.com/Illumina/paragraph⁠.

Accurate genotyping of known variants is a critical for the analysis of whole-genome sequencing data. Paragraph aims to facilitate this by providing an accurate genotyper for Structural Variations with short-read data.

Please reference Paragraph using:

Chen, et al (2019) Paragraph: A graph-based structural variant genotyper for short-read sequence data. bioRxiv. doi: https://doi.org/10.1101/635011⁠ Genotyping data in this paper can be found at paper-data/download-instructions.txt

For details of population genotyping, please also refer to:

https://www.illumina.com/science/genomics-research/accurate-genotyping-of-structural-variant.html⁠