Bulk NGS/allele quantification – Highly efficient generation of isogenic pluripotent stem cell models using prime editing
Output Details
This file contains sequencing results for amplicons covering specific regions of interest related to prime editing of hPSCs
- DNA WGS
- Human
- In Vitro
- iPSC
Meet the Authors
-
Khaja Mohieddin Syed
External Collaborator
-
Oriol Busquets Figueras
External Collaborator
-
Hanqin Li
External Collaborator
-
Yogendra Verma
External Collaborator
-
-
-
-
-
Nitzan Kutnowski
External Collaborator
Related Research
Integrating Long-Read Structural Variant Analysis with single-nucleus RNA-seq to Elucidate Gene Expression Effects in Disease
Long-read sequencing in PD brain samples identified 74,552 structural variants. Integrating RNA sequencing data revealed SVs near PD-related genes impacting cell type-specific expression, highlighting the importance of SVs in complex diseases.
Long read whole genome sequencing data from brain postmortem tissue
Dataset includes 172 whole genome sequencing runs from healthy controls and Parkinson's disease patients, sequenced on Oxford Nanopore platform. Data mapped to T2T-CHM13v2.0 reference genome, available in CRAM format.