Skip to content

Commit 44f7403

Browse files
committed
updated entries
1 parent 3e3d4d2 commit 44f7403

File tree

3 files changed

+25
-5
lines changed

3 files changed

+25
-5
lines changed

src/pages/outreach/Omics Tools Seminar Series: ARCHS4 2025-02-27.md renamed to src/pages/outreach/Omics Tools Webinar Series: ARCHS4 2025-02-27.md

Lines changed: 3 additions & 3 deletions
Original file line numberDiff line numberDiff line change
@@ -12,11 +12,11 @@ featured: true
1212
image: https://cfde-drc.s3.us-east-2.amazonaws.com/assets/img/archs4-feb-2025-4.png
1313
layout: '@/layouts/Outreach.astro'
1414
link: https://mountsinai.zoom.us/webinar/register/WN_ZXBJyN0SRuCj5LaYoGeXuw#/registration
15-
short_description: The seminar featured ARCHS4, a resource that provides access
15+
short_description: The webinar featured ARCHS, a resource that provides access
1616
to gene and transcript counts uniformly processed from all the human and mouse RNA-seq
1717
experiments deposited by the community in the NCBI Gene Expression Omnibus (GEO).
1818
start_date: '2025-02-27T14:00:00-05:00'
1919
tags: '["workshop"]'
20-
title: 'Omics Tools Seminar Series: ARCHS4'
20+
title: 'Omics Tools Webinar Series: ARCHS4'
2121
---
22-
The seminar featured ARCHS4, a resource that provides access to gene and transcript counts uniformly processed from all the human and mouse RNA-seq experiments deposited by the community in the NCBI Gene Expression Omnibus (GEO).
22+
The webinar featured [ARCHS4](https://maayanlab.cloud/archs4/), a resource that provides access to gene and transcript counts uniformly processed from all the human and mouse RNA-seq experiments deposited by the community in the NCBI Gene Expression Omnibus (GEO). Watch recording [here](https://www.youtube.com/watch?v=BSz4XWFmfkg).
Lines changed: 17 additions & 0 deletions
Original file line numberDiff line numberDiff line change
@@ -0,0 +1,17 @@
1+
---
2+
active: true
3+
cfde_specific: true
4+
dcc:
5+
- LINCS
6+
start_date: '2025-01-23T14:00:00-05:00'
7+
end_date: '2025-01-23T15:00:00-05:00'
8+
featured: true
9+
image: /img/genesetcart_webinar.png
10+
layout: '@/layouts/Outreach.astro'
11+
link: https://mountsinai.zoom.us/webinar/register/WN_ZXBJyN0SRuCj5LaYoGeXuw#/registration
12+
short_description: In this lecture, Giacomo Marino, a Bioinformatics Software Engineer in the Ma'ayan Lab at the Icahn School of Medicine at Mount Sinai, describes a new platform for assembling, augmenting, combining, visualizing, and analyzing gene sets. The platform utilizes LLMs to form hypotheses from datasets produced by NIH Common Fund programs.
13+
tags: '["workshop"]'
14+
title: 'Omics Tools Webinar Series: GeneSetCart
15+
'
16+
---
17+
Converting multi-omics datasets into gene sets facilitates data integration that leads to knowledge discovery. Although there are tools developed to analyze gene sets, only few offer the management of gene sets from multiple sources. GeneSetCart is an interactive web-based platform that enables investigators to gather gene sets from various sources; augment these sets with gene-gene co-expression correlations and protein-protein interactions; perform set operations on these sets such as union, consensus, and intersection; and visualize and analyze these gene sets, all in one place. GeneSetCart supports the upload of single or multiple gene sets, as well as fetching gene sets by searching PubMed for genes co-mentioned with terms in publications. Venn diagrams, heatmaps, UMAP, SuperVenn diagrams, and UpSet plots can visualize the gene sets in a GeneSetCart session to summarize the similarity and overlap among the sets. Users of GeneSetCart can also perform enrichment analysis on their assembled gene sets with external tools. All gene sets in a session can be saved to a user account for reanalysis and sharing with collaborators. GeneSetCart has a gene-set-library crossing feature that enables analysis of gene sets created from several NIH Common Fund programs. For the top overlapping sets from pairs of programs, a large language model (LLM) is prompted to propose possible reasons for the high overlap. Using this feature, two use cases are presented. In addition, users of GeneSetCart can produce publication-ready reports from their uploaded sets. Text in these reports is also assisted with an LLM. Overall, GeneSetCart is a useful resource for biologists without programming expertise to facilitate data integration for hypothesis generation.
Lines changed: 5 additions & 2 deletions
Original file line numberDiff line numberDiff line change
@@ -1,13 +1,16 @@
11
---
22
authors: John Erol Evangelista, Daniel J.B. Clarke, Zhuorui Xie, Stephanie Olaiya, Heesu Kim, Giacomo B. Marino, Anna Byrd, Shivaramakrishna Srinivasan, Sumana Srinivasan, Mano R. Maurya, Sherry L. Jenkins, Andrew D. Lutsky, Lucas Sasaya, Alexander Lachmann, Nasheath Ahmed, Ido Diamant, Ethan Sanchez, Srinivasan Ramachandran, Shankar Subramaniam, Avi Ma’ayan
3-
carousel: false
3+
carousel: true
4+
carousel_link: https://www.biorxiv.org/content/10.1101/2025.02.04.636535v1
5+
carousel_description: LEARN MORE ABOUT THE **CFDE WORKBENCH** BY READING THE PREPRINT ON BIORXIV
6+
image: /img/workbench.png
47
centers:
58
- DRC
69
doi: doi.org/10.1101/2025.02.04.636535
710
featured: false
811
journal: bioRxiv
912
landmark: true
1013
layout: '@/layouts/Publication.astro'
11-
title: ' The CFDE Workbench: Integrating Metadata and Processed Data from Common Fund Programs'
14+
title: 'The CFDE Workbench: Integrating Metadata and Processed Data from Common Fund Programs'
1215
year: 2025
1316
---

0 commit comments

Comments
 (0)