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- 2022
-
Mark
PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions
(
- Contribution to journal › Article
- 2020
-
Mark
A crowdsourced set of curated structural variants for the human genome
(
- Contribution to journal › Article
-
Mark
precisionFDA Truth Challenge V2: Calling variants from short- and long-reads in difficult-to-map regions
2020)(
- Working paper/Preprint › Preprint in preprint archive
- 2019
-
Mark
SVCurator: A Crowdsourcing app to visualize evidence of structural variants for the human genome
2019)(
- Working paper/Preprint › Preprint in preprint archive