About The Consortium of Long Read Sequencing (CoLoRS) is an open coalition of international researchers focused on cataloging and providing frequency information, for all classes of variation found within the human genome, using long-read whole genome sequencing. Variants were merged from 1381 samples for autosomes and chrM, from 982 samples for chrX (samples where genetic sex could be confirmed), and from 516 samples (all male) for chrY. License: Creative Commons Attribution 4.0 International Data Source: 10.5281/zenodo.11511512 Citation: Lake, J. A., & Consortium of Long Read Sequencing (CoLoRS). (2024). Consortium of Long Read Sequencing Database (CoLoRSdb) (v1.0.0) [Data set]. Zenodo. https://doi.org/10.5281/zenodo.11511513
This collection is openly accessible.
Consortium of Long Read Sequencing (CoLoRS) is published on HiFi Solves.