Currently at
@cantinilab.bsky.social - Institut Pasteur & @saezlab.bsky.social - Heidelberg Uni
Tools: https://www.github.com/r-trimbour
Publications: https://tinyurl.com/TrimbourRemi
You can extract DNA region modules & visualize CIRCE's interactions over gene locations.
CIRCE also facilitates #CellOracle or #HuMMuS usage, making it unnecessary to run Cicero (code in R) first.
4/5
You can extract DNA region modules & visualize CIRCE's interactions over gene locations.
CIRCE also facilitates #CellOracle or #HuMMuS usage, making it unnecessary to run Cicero (code in R) first.
4/5
We evaluated scATAC-seq preprocessings using promoter capture Hi-C data. 🧬
TLDR: Best performance came from single-cell inputs directly and from CIRCE metacells! 📊
In contrast, count normalization had a negative impact.
3/5
We evaluated scATAC-seq preprocessings using promoter capture Hi-C data. 🧬
TLDR: Best performance came from single-cell inputs directly and from CIRCE metacells! 📊
In contrast, count normalization had a negative impact.
3/5
Both use pseudo-cells to reduce sparsity. CIRCE proposes a new strategy, whose output is closer to the single-cell profiles. 🛠️
On average, CIRCE uses 5x less memory and runs 150x faster ! 📈
2/5
Both use pseudo-cells to reduce sparsity. CIRCE proposes a new strategy, whose output is closer to the single-cell profiles. 🛠️
On average, CIRCE uses 5x less memory and runs 150x faster ! 📈
2/5
Based on #Cicero 's algorithm (Pliner et al.), it runs ~150x faster, processing an atlas of 700k cells in less than 40 min! ⛷️
Short paper: doi.org/10.1101/2025...
Code: github.com/cantinilab/CIRCE
1/5 ⬇️
Based on #Cicero 's algorithm (Pliner et al.), it runs ~150x faster, processing an atlas of 700k cells in less than 40 min! ⛷️
Short paper: doi.org/10.1101/2025...
Code: github.com/cantinilab/CIRCE
1/5 ⬇️