November 9, 2015
- New features:
- Links to MyCancerGenome.org for mutations
- Improved display of selection samples on the study view page
- "Enrichments" analysis is now run across all genes
- The "Network" tab is now using Cytoscape.js (Adobe Flash is no longer required)
October 6, 2015
- New TCGA data:
- Added data of 763 samples from 12 published studies:
- Small Cell Lung Cancer (U Cologne, Nature 2015)
- Uterine Carcinosarcoma (JHU, Nat Commun 2014)
- Microdissected Pancreatic Cancer Whole Exome Sequencing (UTSW, Nat Commun 2015)
- Pancreatic Neuroendocrine Tumors (JHU, Science 2011)
- Renal Non-Clear Cell Carcinoma (Genentech, Nat Genet 2014)
- Infant MLL-Rearranged Acute Lymphoblastic Leukemia (St Jude, Nat Genet 2015)
- Rhabdomyosarcoma (NIH, Cancer Discov 2014)
- Thymic epithelial tumors (NCI, Nat Genet 2014)
- Pediatric Ewing Sarcoma (DFCI, Cancer Discov 2014)
- Ewing Sarcoma (Institut Cuire, Cancer Discov 2014)
- Cutaneous squamous cell carcinoma (DFCI, Clin Cancer Res 2015)
- Gallbladder Carcinoma (Shanghai, Nat Genet 2014)
August 21, 2015
- All TCGA data updated to the Firehose run of April 16, 2015.
- New feature: Enrichments Analysis finds alterations that are enriched in either altered or unaltered samples.
- Improvement: improved OncoPrint with better performance.
June 3, 2015
- Allowed downloading data in each chart/table in study summary page.
- Added log-rank test p-values to the survival plots in study summary page.
- Improved visualization of patient clinical data in patient-centric view.
- Added option to merge multiple samples for the same patient in OncoPrint.
April 28, 2015
- New features:
- Redesigned query interface to allow selecting multiple cancer studies
- Redesigned Plots tab
January 20, 2015
- All TCGA data updated to the Firehose run of October 17, 2014
- COSMIC data updated to V71
- New features:
- Query page: better search functions to find cancer studies
- OncoPrints now support color coding of different mutation types
- OncoPrints now support multiple clinical annotation tracks
- OncoPrinter tool now supports mRNA expression changes
January 6, 2015
- New feature: You can now view frequencies of mutations and copy-number alterations in the study view. These tables are updated dynamically when selecting subsets of samples.
December 9, 2014
- New TCGA data:
- Added complete and up-to-date clinical data for all TCGA provisional studies
- All TCGA data updated to the Firehose run of July 15, 2014
- New TCGA provisional studies: Esophageal cancer, Pheochromocytoma and Paraganglioma (PCPG)
- New published TCGA studies: Thyroid Cancer and Kidney Chromophobe
- Added data of 172 samples from 4 published studies:
- New features:
- Redesigned Mutual Exclusivity tab
- Added correlation scores for scatter plots on the Plots tab
- Download links to GenomeSpace
October 24, 2014
- Added data of 885 samples from 11 published studies:
- Colorectal Adenocarcinoma Triplets (MSKCC, Genome Biology 2014)
- Esophageal Squamous Cell Carcinoma (ICGC, Nature 2014)
- Malignant Peripheral Nerve Sheath Tumor (MSKCC, Nature Genetics 2014)
- Melanoma (Broad/Dana Farber, Nature 2012)
- Nasopharyngeal Carcinoma (National University Singapore, Nature Genetics 2014)
- Prostate Adenocarcinoma CNA study (MSKCC, PNAS 2014)
- Prostate Adenocarcinoma Organoids (MSKCC, Cell 2014)
- Stomach Adenocarcinoma (TCGA, Nature 2014)
- Stomach Adenocarcinoma (Pfizer and University of Hong Kong, Nature Genetics 2014)
- Stomach Adenocarcinoma (University of Hong Kong, Nature Genetics 2011)
- Stomach Adenocarcinoma (University of Tokyo, Nature Genetics 2014)
August 8, 2014
- Released two new tools
- Oncoprinter lets you create Oncoprints from your own, custom data
- MutationMapper draws mutation diagrams (lollipop plots) from your custom data
May 21, 2014
- All TCGA data updated to the Firehose run of April 16, 2014
May 12, 2014
March 27, 2014
- New features:
- Visualizing of mutations mapped on 3D structures (individual or multiple mutations, directly in the browser)
- Gene expression correlation analysis (find all genes with expression correlation to your query genes)
- The Patient-Centric View now displays mutation frequencies across all cohorts in cBioPortal for each mutation
- The Mutation Details Tab and the Patient-Centric View now display the copy-number status of each mutation
March 18, 2014
- All TCGA data updated to the Firehose run of January 15, 2014
- Updated to the latest COSMIC data (v68)
- Added two new provisional TCGA studies:
- Adrenocortical Carcinoma
- Uterine Carcinosarcoma
- Added mutation data of 898 samples from 11 published studies:
- Hepatocellular Carcinoma (RIKEN, Nature Genetics 2012)
- Hepatocellular Carcinoma (AMC, Hepatology in press)
- Medulloblastoma (Broad, Nature 2012)
- Medulloblastoma (ICGC, Nature 2012)
- Medulloblastoma (PCGP, Nature 2012)
- Multiple Myeloma (Broad, Cancer Cell 2014)
- Pancreatic Adenocarcinoma (ICGC, Nature 2012)
- Small Cell Carcinoma of the Ovary (MSKCC, Nature Genetics in press)
- Small Cell Lung Cancer (CLCGP, Nature Genetics 2012)
- Small Cell Lung Cancer (Johns Hopkins, Nature Genetics 2012)
- NCI-60 Cell Lines (NCI, Cancer Res. 2012)
December 9, 2013
- Added mutation data of 99 bladder cancer samples (BGI, Nature Genetics 2013)
December 6, 2013
- Data sets matching four recently submitted or published TCGA studies are now available
- Glioblastoma (Cell 2013)
- Bladder carcinoma (Nature, in press)
- Head & neck squamous cell carcinoma (submitted)
- Lung adenocarcinoma (submitted)
November 8, 2013
- All TCGA data updated to the Firehose run of September 23, 2013.
- Updated to the latest COSMIC data (v67).
- Added mutation data of 792 samples from 9 published cancer studies:
- Esophageal Adenocarcinoma (Broad, Nature Genetics 2013)
- Head and Neck Squamous Cell Carcinoma (Broad, Science 2011)
- Head and Neck Squamous Cell Carcinoma (Johns Hopkins, Science 2011)
- Kidney Renal Clear Cell Carcinoma (BGI, Nature Genetics 2012)
- Prostate Adenocarcinoma, Metastatic (Michigan, Nature 2012)
- Prostate Adenocarcinoma (Broad/Cornell, Nature Genetics 2012)
- Prostate Adenocarcinoma (Broad/Cornell, Cell 2013)
- Skin Cutaneous Melanoma (Yale, Nature Genetics 2012)
- Skin Cutaneous Melanoma (Broad, Cell 2012)
October 21, 2013
- Improved interface for survival plots, including information on individual samples via mouse-over
- New fusion glyph in OncoPrints
- Improved cross-cancer query: new alteration frequency histogram (example below - query gene: CDKN2A) and mutation diagram
September 9, 2013
- Updated COSMIC data (v66 Release)
- Improved / interactive visualization on the "Protein changes" tab
- Enhanced mutation diagrams: color-coding by mutation time and syncing with table filters
- Addition of DNA cytoband information in the patient view of copy-number changes
- OncoPrints now allow the display of an optional track with clinical annotation (Endometrial cancer example below)
July 25, 2013
- Multi-gene correlation plots.
- Variant allele frequency distribution plots for individual tumor samples.
- Tissue images for TCGA samples in the patient view, via Digital Slide Archive. Example.
July 16, 2013
- All TCGA data updated to the May Firehose run (May 23, 2013).
- TCGA Pancreatic Cancer study (provisional) added.
July 4, 2013
- Improved rendering of mutation diagrams, including ability to download in PDF format.
- Improved home page: Searchable cancer study & gene set selectors, data sets selector.
June 17, 2013
- Improved interface for correlation plots, including information on individual samples via mouse-over.
- Gene Details from Biogene are now available in the Network view.
- Added mutation and copy number data from a new adenoid cystic carcinoma study: Ho et al., Nature Genetics 2013.
- Added mutation data from 6 cancer studies.
- Breast Invasive Carcinoma (Shah et al., Nature 2012)
- Breast Invasive Carcinoma (Banerji et al., Nature 2012)
- Breast Invasive Carcinoma (Stephens et al., Nature 2012)
- Lung Adenocarcinoma (Imielinksi et al., Cell 2012)
- Lung Adenocarcinoma (Ding et al., Nature 2008)
- Colorectal Cancer (Seshagiri et al., Nature 2012)
June 4, 2013
- All TCGA data updated to the April Firehose run (April 21, 2012).
May 14, 2013
- Added a published TCGA study: Acute Myeloid Leukemia (TCGA, NEJM 2013).
April 28, 2013
- All TCGA data updated to the March Firehose run (March 26, 2012).
- mRNA percentiles for altered genes shown in patient view.
April 2, 2013
- All TCGA data updated to the February Firehose run (February 22, 2012).
March 28, 2013
- All TCGA data updated to the January Firehose run (January 16, 2012).
- Data from a new bladder cancer study from MSKCC has been added (97 samples, Iyer et al., JCO in press).
February 16, 2013
- The cBio Portal now contains mutation data from all provisional TCGA projects. Please adhere to the TCGA publication guidelines when using these and any TCGA data in your publications.
- All data updated to the October Firehose run (October 24, 2012).
- Sequencing read counts and frequencies are now shown in the Mutation Details table when available.
- Improved OncoPrints, resulting in performance improvements.
November 21, 2012
- Major new feature: Users can now visualize genomic alterations and clinical data of individual tumors, including:
- Summary of mutations and copy-number alterations of interest
- Clinical trial information
- TCGA Pathology Reports
- New cancer summary view (Example Endometrial Cancer)
- Updated drug data from KEGG DRUG and NCI Cancer Drugs (aggregated by PiHelper)
October 22, 2012
- All data updated to the Broad Firehose run from July 25, 2012.
- COSMIC data added to Mutation Details (via Oncotator).
- All predicted functional impact scores are updated to Mutation Assessor 2.0.
- Users can now base queries on genes in recurrent regions of copy-number alteration (from GISTIC via Firehose).
- The Onco Query Language (OQL) now supports queries for specific mutations or mutation types.
- Data sets added that match the data of all TCGA publications (GBM, ovarian, colorectal, and lung squamous).
July 18, 2012
- Mutation data for the TCGA lung squamous cell carcinoma and breast cancer projects (manuscripts in press at Nature).
- All data updated to the latest Broad Firehose run (May 25, 2012).
- Drug information added to the network view (via Drugbank).
- Improved cross-cancer queries: Option to select data types, export of summary graphs.
- Users can now base queries on frequently mutated genes (from MutSig via Firehose).
May 16, 2012
- All data updated to the latest Broad Firehose run (March 21, 2012).
- Extended cross-cancer functionality, enabling users to query across all cancer studies in our database.
- New "build a case" functionality, enabling users to generate custom case sets, based on one or more clinical attributes.
- New OncoPrint features, including more compact OncoPrints, and support for RPPA visualization.
February 27, 2012
- All data updated to the latest Broad Firehose run (January 24, 2012).
- Validated mutation data for colorectal cancer.
- New feature: Mutation Diagrams that show mutations in the context of protein domains.
January 30, 2012
- Updated data for several TCGA cancer studies.
- Some small bug-fixes.
December 22, 2011
- Fourteen new TCGA cancer studies: This includes complete data for TCGA Colorectal Carcinoma
and provisional data for thirteen other cancer types in the TCGA production pipeline. Please note that data from these
thirteen new cancer types are provisional, not final and do not yet include mutation data.
As per NCI guidelines, preliminary mutation data cannot be redistributed until they have been validated.
- Four new data types:
- Reverse-phase protein array (RPPA) data.
- microRNA expression and copy-number (including support for multiple loci)
- RNA-Seq based expression data.
- log2 copy-number data.
- Updated TCGA GBM copy-number, expression, and methylation data.
- New gene symbol validation service. You can now use gene aliases and/or Entrez Gene IDs within your gene sets.
- Links to IGV for visualization of DNA copy-number changes.
- Background information from the Sanger Cancer Gene Census.
- Two new Tutorials to get you quickly started in using the portal.
November 14, 2011
- New and improved mutation details, with sorting and filtering capabilities.
- In collaboration with Bilkent University, we have added a new Network tab to our results pages. The network tab enables users to visualize, analyze and filter cancer genomic data in the context of pathways and interaction networks derived from Pathway Commons.
September 3, 2011
- You can now query across different cancer studies (feature available directly from the home page).
- Our MATLAB CGDS Cancer Genomics Toolbox is now available. The toolbox enables you to download data from the cBio Portal, and import it directly into MATLAB.
- The code for the cBio Portal has now been fully open sourced, and made available at Google Code. If you would like to join our open source efforts and make the portal even better, drop us an email.
March 2, 2011
New plotting features and other improvements:
- Correlation plots that show the relationship between different data types for individual genes.
- Survival analysis - assess survival differences between altered and non-altered patient sets.
- Updated R Package with support for correlation plots and general improvements for retrieving and accessing data in R data frames.
- The Web Interface now supports basic clinical data, e.g. survival data.
- Networks for pathway analysis are now available for download.
December 15, 2010
Several new features, including:
- Redesigned and streamlined user interface, based on user feedback and usability testing.
- Advanced support for gene-specific alterations. For example, users
can now view mutations within TP53, and ignore copy number alterations, or
only view amplifications of EGFR, and ignore deletions.
- Improved performance.
- Frequently Asked Questions document released.
- Updated Video Tutorial.
November 4, 2010
- Enhanced Oncoprints, enabling users to quickly visualize genomic alterations across many cases. Oncoprints now also work in all major browsers, including Firefox, Chrome, Safari, and Internet Explorer.
- Official release of our Web Interface, enabling programmatic access to all data.
- Official release of our R Package, enabling programmatic access to all data from the R platform for statistical computing.
New Jobs available at Dana-Farber to work on cBioPortal Or follow us @cbioportal on Twitter
RAS/RAF alterations in colorectal cancer
BRCA1 and BRCA2 mutations in ovarian cancer
POLE hotspot mutations in endometrial cancer
TP53 and MDM2/4 alterations in GBM
PTEN mutations in GBM in text format
BRAF V600E mutations across cancer types
Patient view of an endometrial cancer case
What People are Saying
"Whenever bench scientists ask me how they can look at TCGA data, I've never
had a good answer for them. Now I do. The cBio Portal meets a critical need--it is the
interface that the cancer research community needs to access the wealth of TCGA. Even as a
computational biologist, I use it to follow-up on genes of interest. It makes querying
the data much less painful."
– Postdoctoral Fellow, Oregon Health & Science University
"I would like to congratulate you and the team of the cBio portal.
It's just an amazing tool to work with, and we at Mass General really appreciate it."
– Research Fellow at Massachusetts General Hospital
"As a bench biologist with primary aim of determining gene aberrations in GBM, I found
your site absolutely fantastic! Thank you! I have to reiterate how awesome and user-friendly
your group has made this site - finally accomplishing the goal of having data easily accessible
– Sr. Research Associate at Knight Cancer Institute/OHSU
"Thank you for your incredible resource that has helped greatly in accessing the TCGA
– Postdoctoral Fellow, Johns Hopkins University School of Medicine,
Dept Radiation Oncology and Molecular Radiation Sciences
"I have been enjoying the ease with which TCGA data can be extracted in R using your CGDS package.
Very nice work!"
– Sr. Software Engineer, Institute for Systems Biology
"Thank you for generating such an excellent software. It is very useful for our research."
– Research Fellow, Memorial Sloan-Kettering Cancer Center
"Thank you very much for providing and maintaining this great resource."
– Scientist, Discovery Bioinformatics, Biotechnology Company
"I want to thank you for the nice, useful and user-friendly interface you have generated
and shared with the community."
– Postdoctoral Fellow, Harvard Medical School, Children's Hospital Boston
"This portal is truly the greatest thing since sliced bread. I am making discoveries with it not only in glioblastoma, my primary focus, but in other cancers as well -- it's all so easy with this fantastic tool. And I am enjoying showing it to my colleagues, whose jaws also drop. Thank you a thousand times over for this beautiful public resource. I am looking forward to citing this soon in an upcoming paper..."
– Associate Professor, University of Virginia