正在加载视频...

视频加载失败

here comes WebAtlas: our "Google Maps" for tissue atlases with integrated single cell and spatial transcriptomics so anyone & anywhere can access/explore atlas datasets on a web browser. Fantastic collab with Muzlifah Haniffa, led by Tong LI 李彤 Dave Horsfall & Daniela. Links 👇

52,996 次观看 • 3 年前 •via X (Twitter)

17 条评论

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

Paper: Portal where you can access datasets:

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

The integration of single cell + spatial transcriptomics can build awesome tissue atlases but it is hard to share these datasets in a globally accessible & usable format without technical burden on the users. We aimed to solve this problem with WebAtlas

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

WebAtlas addresses 2 key challenges in this area: 1) how to deal with myriad technologies and data types in sc/spatial omics? and 2) how to freely browse integrated datasets?

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

The core of WebAtlas is a data ingestion pipeline that unifies data types from nearly all commonly used atlassing technologies (works on sc/snRNAseq, Visium, Xenium, MERSCOPE, In Situ Sequencing, seqFISH) into the cloud-optimised & scalable Zarr format @zarr_dev

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

We put special care into image components of spatial data i.e. raw images and cell segmentation masks are handled as OME-Zarr for multi-scale visualisation. This was a parallel effort with SpatialData & we are keen to support their format in the future

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

We then re-used the awesome Vitessce web visualisation framework from @ngehlenborg that allows fully interactive exploration of sc + ST data. We customised it for coordinated browsing of cell types & gene expression in integrated sc and ST datasets

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

We showcased WebAtlas on a "triple" modality atlas of the developing human hindlimb from @teichlab that combines scRNAseq, Visium spatial RNA-Seq and In Situ Sequencing (ISS done by @krobertssci in my lab). You can explore it on & few more tweets below.

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

We harmonised cell types & gene expression across 3X modalities with computational integration: our Cell2location tool to integrate scRNAseq + Visium and StabMap from @shazanfar to transfer cell types & impute gene expression from scRNA-seq to ISS (

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

The result is stunning WebAtlas (the video on top) where you can cross-query cell types & genes across all modalities in one place, where you can browse the ISS spatial cell map to explore the beautiful structure of the developing bone, muscle and skin across the embryonic limb.

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

Many fun things to do on the integrated atlas. For example, the scRNAseq -> ISS imputation allowed us to identify a novel spatial gene expression gradient in chondroprogenitors that give rise to the cartilage anlage! On WebAtlas, you can cross-validate this on Visium data!

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

WebAtlas is tech agnostic and supports many technologies as listed above e.g. see a Xenium dataset of a human breast tumour on WebAtlas here

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

...and an integrated scRNA-seq + seqFISH atlas of mouse embryogenesis from @MarioniLab ( - webAtlas link here:

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

Finally, WebAtlas is scalable: to date it has handled scRNAseq with 900k cells and MERSCOPE with 700k cells Currently works best with <10 Million RNA molecules

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

Try WebAtlas! Our landing page with all datasets tweeted above & shown in paper: Repo: Tutorials:

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

I am excited about sharing our upcoming @humancellatlas datasets with the community on WebAtlas and a future where we can build "Next-Gen" multi-modal tissue atlases on the cloud. If you are interested, please reach out!

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

This was a wonderful collab with @Muzz_Haniffa @BioinfoTongLI @Dave_Horsfall @krobertssci @PengHeCam @shazanfar @teichlab. Special thx to @notjustmoore who aligned us with SpatialData from @fabian_theis and @OliverStegle...

Omer Ali Bayraktar 的头像
Omer Ali Bayraktar3 年前

..., @zarr_dev & Vitessce @ngehlenborg & @openmicroscopy teams for our technical foundations, and @wellcometrust @sangerinstitute for supporting our work!

相关视频

Excited to share our new work on building a multimodal atlas of human skin in health and inflammatory disease — a project I’m especially proud of, bringing together AI, high-throughput genomics, and clinical science to accelerate discovery. Over the past decade, single-cell genomics has transformed how we map cells in human tissues. But a major challenge remains: can we systematically decode how cells organize into functional niches in situ — including those invisible to standard histopathology? To address this, we integrated large-scale scRNA-seq, spatial transcriptomics, histopathology, and AI-driven modeling frameworks to build an in situ atlas of human skin across health and disease. Led by Lloyd Steele, an MD/PhD student working between Haniffa Lab and my lab at Wellcome Sanger Institute and Cambridge University . Another amazing collaboration with Muzz Haniffa, the mastermind behind the work as part of Human Cell Atlas. A key part of this study is that we didn’t build everything from scratch — we leveraged and combined AI methods that actually work! and showed how they can be used together to extract biological insight at scale. We used: • scArches to build and map into a reference scRNA-seq atlas of human skin: • NicheCompass to identify and characterize spatial niches: • MINT-Flow to extract microenvironment-induced cell states and gene programs: Together, these enabled an end-to-end workflow from atlas construction to spatial mapping, niche discovery, and cell state decoding. At scale, we integrated ~5 million cells and 100+ spatial sections, enabling a systematic view of tissue organization. Using this framework, we identified 26 niches in skin, including known histopathologic structures as well as hidden disease-associated niches not visible on H&E. Among the most striking findings were a resident memory T cell-rich sebaceous gland niche and a plasma cell-rich sweat gland niche, suggesting that appendageal structures act as active immunological microenvironments and may contribute to inflammatory memory and disease persistence. Importantly, this atlas is not just descriptive — it is usable. It can support mapping of new datasets, resolve finer cell types and niches, extract microenvironment-driven programs, and enable predictive analyses at scale. More broadly, this work shows what becomes possible when AI, spatial genomics, and atlas-scale data are integrated end-to-end: not just mapping tissues, but systematically decoding them. This was a massive collaboration, and I’m very grateful to the amazing scientists April Foster, Kenny Roberts, and Chloe Admane. Lloyd is an amazing scientist, and I’m especially excited for the community to see more of his work soon — stay tuned. The data and pre-trained models will be released soon. Preprint:

Mo Lotfollahi

11,759 次观看 • 3 个月前