生物
诱导多能干细胞
计算生物学
清脆的
基因组编辑
表型
Cas9
干细胞
基因
基因组
遗传学
胚胎干细胞
作者
Caroline B. Pantazis,Andrian Yang,Erika Lara,Justin A. McDonough,Cornelis Blauwendraat,Lirong Peng,Hideyuki Oguro,Jitendra Kumar Kanaujiya,Jizhong Zou,David P. Sebesta,Gretchen Pratt,Erin Cross,Jeffrey Blockwick,Philip Buxton,Lauren Kinner-Bibeau,Constance Medura,Christopher Tompkins,Stephen H. Hughes,Marianita Santiana,Faraz Faghri
出处
期刊:Cell Stem Cell
[Elsevier BV]
日期:2022-12-01
卷期号:29 (12): 1685-1702.e22
被引量:304
标识
DOI:10.1016/j.stem.2022.11.004
摘要
Human induced pluripotent stem cell (iPSC) lines are a powerful tool for studying development and disease, but the considerable phenotypic variation between lines makes it challenging to replicate key findings and integrate data across research groups. To address this issue, we sub-cloned candidate human iPSC lines and deeply characterized their genetic properties using whole genome sequencing, their genomic stability upon CRISPR-Cas9-based gene editing, and their phenotypic properties including differentiation to commonly used cell types. These studies identified KOLF2.1J as an all-around well-performing iPSC line. We then shared KOLF2.1J with groups around the world who tested its performance in head-to-head comparisons with their own preferred iPSC lines across a diverse range of differentiation protocols and functional assays. On the strength of these findings, we have made KOLF2.1J and its gene-edited derivative clones readily accessible to promote the standardization required for large-scale collaborative science in the stem cell field.
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