Explore >2900 public resources instantly
R2 makes data not only FAIR, but also usable for scientists
No bioinformatics expertise needed
3100+ citations in PubMed
r2platform.com
Explore >2900 public resources instantly
R2 makes data not only FAIR, but also usable for scientists
No bioinformatics expertise needed
3100+ citations in PubMed
r2platform.com
Explore >2900 public resources instantly
R2 makes data not only FAIR, but also usable for scientists
No bioinformatics expertise needed
3100+ citations in PubMed
r2platform.com
Explore >2900 public resources instantly
R2 makes data not only FAIR, but also usable for scientists
No bioinformatics expertise needed
3100+ citations in PubMed
r2platform.com
'Rapid genome-wide epigenomic classification of acute #leukemia'.
Includes embeddings of the paper, as well as UMAP parameter sweeps.
R2 open online nocode data #science platform for biomedical researchers
r2platform.com
3.100+ citations in PubMed 🧪
'Rapid genome-wide epigenomic classification of acute #leukemia'.
Includes embeddings of the paper, as well as UMAP parameter sweeps.
R2 open online nocode data #science platform for biomedical researchers
r2platform.com
3.100+ citations in PubMed 🧪
Elucidating and #Pharmacologic Targeting of Coexisting Diffuse Midline Subpopulation Dependencies
Assessment of 9 #compounds in a #DIPG xenograft
R2 makes data FAIR & usable for scientists. No bioinformatics expertise needed
3100+ citations in PubMed
Elucidating and #Pharmacologic Targeting of Coexisting Diffuse Midline Subpopulation Dependencies
Assessment of 9 #compounds in a #DIPG xenograft
R2 makes data FAIR & usable for scientists. No bioinformatics expertise needed
3100+ citations in PubMed
Functional diversity of inhibitors tackling the differentiation arrest of MLL-rearranged #leukemia
Explore >2900 public resources instantly
R2 makes data not only FAIR, but also usable for scientists. No bioinformatics expertise needed
3100+ citations in #pubMed
Functional diversity of inhibitors tackling the differentiation arrest of MLL-rearranged #leukemia
Explore >2900 public resources instantly
R2 makes data not only FAIR, but also usable for scientists. No bioinformatics expertise needed
3100+ citations in #pubMed
#Colorectal #cancer cell lines with SETDB1 depletion
Explore >2900 public resources instantly.
R2 makes data not only FAIR, but also usable for scientists. No bioinformatics expertise needed.
3100+ citations in #pubMed
#Colorectal #cancer cell lines with SETDB1 depletion
Explore >2900 public resources instantly.
R2 makes data not only FAIR, but also usable for scientists. No bioinformatics expertise needed.
3100+ citations in #pubMed
r2platform.com
r2platform.com
We have included most of the suggestions suggested and released these in a fresh update :)
r2platform.com
We have included most of the suggestions suggested and released these in a fresh update :)
r2platform.com
Play with it in the recent 3D-UMAP addition of R2
Play with it in the recent 3D-UMAP addition of R2
R2: open online nocode data science platform for biomedical researchers
Secure your free account Today at r2platform.com
R2: open online nocode data science platform for biomedical researchers
Secure your free account Today at r2platform.com
Check the R2 Introduction Workshop and training programme for step‑by‑step courses, from basics to advanced pipelines: r2-training-courses.readthedocs.io
Check the R2 Introduction Workshop and training programme for step‑by‑step courses, from basics to advanced pipelines: r2-training-courses.readthedocs.io
Follow the “Differential expression” tutorial to compare groups, generate gene lists, and move on to pathway/GO exploration within the same interface.
Follow the “Differential expression” tutorial to compare groups, generate gene lists, and move on to pathway/GO exploration within the same interface.
Try the tutorials on heatmaps and clustering to visualize gene sets, patterns, and subgroups in your data. The guided “short story” style walks you through each click.
Try the tutorials on heatmaps and clustering to visualize gene sets, patterns, and subgroups in your data. The guided “short story” style walks you through each click.
Use the “View a gene” entry point, select your dataset, and type a gene symbol. R2 instantly shows expression plots and associations with clinical or molecular annotations.
Use the “View a gene” entry point, select your dataset, and type a gene symbol. R2 instantly shows expression plots and associations with clinical or molecular annotations.
Go to r2platform.com and choose a public dataset from the landing page. R2 hosts many preloaded studies so you can start analyzing immediately—no upload, no install.
Go to r2platform.com and choose a public dataset from the landing page. R2 hosts many preloaded studies so you can start analyzing immediately—no upload, no install.
R2 is a free, web-based environment to explore large-scale transcriptomics and other omics data without coding. Start here: r2-tutorials.readthedocs.io/en/latest/ 🧪
R2 is a free, web-based environment to explore large-scale transcriptomics and other omics data without coding. Start here: r2-tutorials.readthedocs.io/en/latest/ 🧪
R2 open online #nocode data science platform for biomedical #scientists
No #bioinformatics / coding expertise needed.
Join the community and secure your FREE account Today
r2platform.com
R2 open online #nocode data science platform for biomedical #scientists
No #bioinformatics / coding expertise needed.
Join the community and secure your FREE account Today
r2platform.com
R2 open online #nocode data #science platform for #biomedical #researchers
r2platform.com
R2 open online #nocode data #science platform for #biomedical #researchers
r2platform.com
Translated retained intron 11 sequence confers pathological properties to Tau in Alzheimer’s disease from #article in Prog Neurobiol
R2 open online nocodde data science platform for biomedical scientists. No bioinformatics / coding expertise needed
r2platform.com
Translated retained intron 11 sequence confers pathological properties to Tau in Alzheimer’s disease from #article in Prog Neurobiol
R2 open online nocodde data science platform for biomedical scientists. No bioinformatics / coding expertise needed
r2platform.com
R2 open online #nocode data #science platform for biomedical #researchers. No #bioinformatics expertise needed
Join the community and secure your FREE account Today r2platform.com
R2 open online #nocode data #science platform for biomedical #researchers. No #bioinformatics expertise needed
Join the community and secure your FREE account Today r2platform.com
R2 open online #nocode data #science platform for biomedical researchers
free Today r2platform.com
R2 open online #nocode data #science platform for biomedical researchers
free Today r2platform.com
Gene expression profile of Kelly and SH-SY5Y cells after treatment with retinoic acid
R2 open online nocode data science platform for biomedical researchers
r2platform.com
3.000+ citations in PubMed
Secure your FREE account Today
Gene expression profile of Kelly and SH-SY5Y cells after treatment with retinoic acid
R2 open online nocode data science platform for biomedical researchers
r2platform.com
3.000+ citations in PubMed
Secure your FREE account Today
TEAD switches interacting partners along neural #progenitor lineage progression to execute distinct functions
R2 open online data #science platform 4 biomedical #researchers
r2platform.com
3k+ citations in PubMed
Secure your FREE account
TEAD switches interacting partners along neural #progenitor lineage progression to execute distinct functions
R2 open online data #science platform 4 biomedical #researchers
r2platform.com
3k+ citations in PubMed
Secure your FREE account
R2 open online nocode data #science platform for biomedical #researchers r2platform.com
Instantly explore #genomics data from the comfort of your browser
3000+ citations in PubMed
Secure your FREE account
R2 open online nocode data #science platform for biomedical #researchers r2platform.com
Instantly explore #genomics data from the comfort of your browser
3000+ citations in PubMed
Secure your FREE account