Figshare+
Browse
.SVS
19347.svs (967.47 MB)
.SVS
19139.svs (950.97 MB)
.SVS
18762.svs (847.23 MB)
.SVS
18688.svs (812.95 MB)
.SVS
19680.svs (802.64 MB)
.SVS
19105.svs (801.32 MB)
.SVS
18695.svs (783.15 MB)
.SVS
19481.svs (775.99 MB)
.SVS
18796.svs (763.94 MB)
.SVS
18804.svs (755.39 MB)
.SVS
18545.svs (753.43 MB)
.SVS
18741.svs (752.03 MB)
.SVS
19358.svs (742.34 MB)
.SVS
18691.svs (734.05 MB)
.SVS
18699.svs (730.88 MB)
.SVS
19267.svs (728.33 MB)
.SVS
19184.svs (726.04 MB)
.SVS
18690.svs (723.66 MB)
.SVS
19354.svs (722.53 MB)
.SVS
18747.svs (720.97 MB)
1/0
1292 files

Training Cohort Slide Images for "Intratumoral resolution of driver gene mutation heterogeneity in renal cancer using deep learning"

dataset
posted on 2022-06-07, 05:36 authored by Satwik RajaramSatwik Rajaram, Paul Acosta, Vandana Panwar, Vipul Jarmale, Alana Christie, Jay Jasti, Vitaly Margulis, Dinesh Rakheja, John Cheville, Bradley C Leibovich, Alexander Parker, James Brugarolas, Payal Kapur

This item contains whole slide images (in SVS format) of all samples from the Training cohort analyzed in the paper "Intratumoral resolution of driver gene mutation heterogeneity in renal cancer using deep learning" by Acosta et al in Cancer Research (https://doi.org/10.1158/0008-5472.CAN-21-2318). This work demonstrates that deep learning (DL) models can predict the intratumor heterogeneity in driver mutation status purely from Hematoxylin and Eosin (H&E) stained slides.


Specifically, we trained and validated DL models that predict the status of three of the most frequently mutated driver genes (BAP1, PBRM1, and SETD2) in clear cell renal cell carcinoma. The DL models were trained on a large cohort of whole slide images (N=1282, referred to as WSI cohort in the paper/code) and tested on several independent cohorts including the TCGA KIRC (N=363 patients), two human tissue microarray (TMA) cohorts (referred to as TMA1 with 118 patients and TMA2 with 365 patients respectively) and a patient-derived xenograft TMA (referred to as PDX1).


The current dataset contains the H&E stained whole slide images for the WSI cohort. 


See related materials in collection at: https://doi.org/10.25452/figshare.plus.c.5983795

Funding

NIH (P50 CA196516) CPRIT (RP180192) CPRIT (RP180191) NIH (R01CA244579 , R01CA154475 , and R01DK115986) DOD ( W81XWH1910710 ) CPRIT ( RP200233 ). Lyda Hill Department of Bioinformatics

University of Texas Southwestern Medical Center SPORE in Kidney Cancer

National Cancer Institute

Find out more...

Dissecting the interplay between BAP1 and PBRM1 in renal cancer

Cancer Prevention and Research Institute of Texas

Find out more...

Understanding TFE3-mediated Tumorigenesis through Analysis of a Novel, Clinically-Relevant Mouse Model of Translocation Renal Cell Carcinoma

Cancer Prevention and Research Institute of Texas

Find out more...

Vascular image-guided optimization of response (VIGOR) to therapy in kidney cancer

National Cancer Institute

Find out more...

NON-INVASIVE PHYSIOLOGIC PREDICTORS OF AGGRESSIVENESS IN RENAL CELL CARCINOMA

National Cancer Institute

Find out more...

Glomerular Filtration of Sub-nm Gold Nanoparticles

National Institute of Diabetes and Digestive and Kidney Diseases

Find out more...

Advance CT And Fluorescence Imaging Of Kidney Cancers With Glutathione-mediated Contrast Enhancements

Cancer Prevention and Research Institute of Texas

Find out more...

History

Research Institution(s)

University of Texas Southwestern Medical Center, Mayo Clinic

I confirm there is no human personally identifiable information in the files or description shared

  • Yes

I confirm the files and description shared may be publicly distributed under the license selected

  • Yes