Closed flyfyyfyy closed 1 week ago
Hi @flyfyyfyy,
HEST-1k was initially designed to match H&E crops and ST spots. Xenium transcripts have been pooled into pseudo-Visium (squared spots). As it seems that many people are interested in Xenium, we will be releasing aligned H&E with Xenium/DAPI at cell-level + the list of all transcripts.
Having perfect alignment takes time as Xenium explorer tools don't scale well. We are using a sota whole-slide registration instead. More information here: https://github.com/mahmoodlab/HEST/issues/38.
The release is expected for next Friday.
Hi @guillaumejaume
Which sota whole-slide registration tool did you use to align the HE image with Xenium?
A slightly modified version of Valis, https://github.com/MathOnco/valis.
Hi @flyfyyfyy, @kennethahah,
The aligned transcripts are now available on HF along with 121 new samples.
We apologize for coming back to you this late, registration took more time than expected.
Tutorial has been updated: https://github.com/mahmoodlab/HEST/blob/main/tutorials/2-Interacting-with-HEST-1k.ipynb
Hi,
The Xenium are imaging-based ST technology so that the Xenium dataset's spatial coordinates are not supposed to be grid. Why does the TENX99 dataset have the grid coordinates.
I check the raw data from 10x genomics replicate 1, https://www.10xgenomics.com/datasets/ffpe-human-breast-using-the-entire-sample-area-1-standard. The cells matrix in raw data.
And I only get 280 genes for each spot and 892965 spots in raw data. But 23060 spots in HEST TENX99. So, how do you guys pre-process the Xenium dataset here?