mantispy.ds.aconcagua#
- mantispy.ds.aconcagua(cache_dir=None)[source]#
Aconcagua, a genome-scale optical pooled CRISPR screen of essential genes in HeLa cells.
One row per guide per well: the median profile of a guide’s cells in a well, after a per plate-and-well robust normalization against the well’s non-targeting controls, over a subset of the screen built for the optical-pooled-screens case study. The cells were segmented and measured with brieflow’s
cp_emulatorin four channels (DNA, alpha-tubulin, gamma-H2AX and F-actin); the brieflow feature names are mapped to mantispy’s CellProfiler-style grammar. The subset keeps all 250 non-targeting guides, four annotated positive controls (H2AX, ECT2, TUBB, CFL1), 50 strong and 50 weak known hits, and 396 random library genes, across eight plates and 46 wells.Mitotic cells are pooled at their natural share rather than capped, so a profile mixes interphase and mitotic cells as the screen saw them, and each row records its
Metadata_MitoticFraction. The file is staged onscverse-exampledata, so the loader fetches a single h5ad rather than rebuilding it from the raw per-cell table.- Parameters:
cache_dir (
str|Path|None(default:None)) – Where to keep the download. Defaults tomantispy.settings.cache_dir.- Return type:
- Returns:
Guide-by-well profiles read with
mantispy.io.read(), carryingMetadata_Plate,Metadata_Well,Metadata_Guide,Metadata_Gene,Metadata_Perturbation(the gene, or"nontargeting"),Metadata_Perturbation_Type("crispr"),Metadata_ControlandMetadata_Control_Type(negcon/poscon/treatment),Metadata_Tier(control/strong/weak/random),Metadata_CellCountandMetadata_MitoticFraction.
References
Di Bernardo and others [2026], this screen; [Funk et al., 2022], the screen it extends. The per-cell measurements are from brieflow; the subset is available through the CZ Biohub OPS Explorer.