Leila Sidow

ORCID: 0000-0003-1246-7225
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About
Contact & Profiles
Research Areas
  • Single-cell and spatial transcriptomics
  • RNA Research and Splicing
  • CRISPR and Genetic Engineering
  • Genomics and Chromatin Dynamics
  • Neuroscience and Neuropharmacology Research
  • Pluripotent Stem Cells Research
  • Environmental DNA in Biodiversity Studies
  • Forensic and Genetic Research
  • dental development and anomalies

Max Planck Institute for Evolutionary Anthropology
2019-2021

Abstract Induced pluripotent stem cell (iPSC)-derived organoids provide models to study human organ development. Single-cell transcriptomics enable highly resolved descriptions of states within these systems; however, approaches are needed directly measure lineage relationships. Here we establish iTracer, a recorder that combines reporter barcodes with inducible CRISPR–Cas9 scarring and is compatible single-cell spatial transcriptomics. We apply iTracer explore clonality dynamics during...

10.1038/s41592-021-01344-8 article EN cc-by Nature Methods 2021-12-30

Diverse regions develop within cerebral organoids generated from human induced pluripotent stem cells (iPSCs), however it has been a challenge to understand the lineage dynamics associated with brain regionalization. Here we establish an inducible recording system that couples reporter barcodes, CRISPR/Cas9 scarring, and single-cell transcriptomics analyze relationships during organoid development. We infer fate-mapped whole phylogenies over scarring time course, reconstruct...

10.1101/2020.06.19.162032 preprint EN cc-by-nc bioRxiv (Cold Spring Harbor Laboratory) 2020-06-20

Induced pluripotent stem cells (iPSCs) from diverse humans offer the potential to study human functional variation in controlled culture environments. A portion of this originates an ancient admixture between modern and Neandertals, which introduced alleles that left a phenotypic legacy on individual today. Here, we show large iPSC repository harbors extensive Neandertal DNA, including contribute phenotypes diseases, encode hundreds amino acid changes, alter gene expression specific tissues....

10.1016/j.stemcr.2020.05.018 article EN cc-by-nc-nd Stem Cell Reports 2020-06-18

ABSTRACT The human brain has changed dramatically since humans diverged from our closest living relatives, chimpanzees and the other great apes 1–5 . However, genetic developmental programs underlying this divergence are not fully understood 6–8 Here, we have analyzed stem cell-derived cerebral organoids using single-cell transcriptomics (scRNA-seq) accessible chromatin profiling (scATAC-seq) to explore gene regulatory changes that specific humans. We first analyze cell composition...

10.1101/685057 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2019-06-27
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