Bioconductor home page and help material -- 'man' pages, vignettes, work flows, courses & conferences (including static resources), user support forum & devel mailing list, twitter, newsletter, community contributions, publications, etc. Introductory video.

Few scientific 3D-printable models are available online, and the expertise required to generate and validate such models remains a barrier. The NIH 3D Print Exchange eliminates this gap with an open, comprehensive, and interactive website for searching, browsing, downloading, and sharing biomedical 3D print files, modeling tutorials, and educational material.

The overall mission of the Oncogenomics section of the Pediatric Oncology Branch, is to leverage the power of genome wide high-throughput approaches to improve the outcome of patients with high risk cancers, with a focus on neuroblastoma.

The Cancer Imaging Archive (TCIA) requires users to register to be able to search images. Registration is free and open to anyone. We are asking users to register in order to gather general usage statistics in order to inform future enhancements in the service provided by this site.

The Clinical Proteomic Tumor Analysis Consortium (CPTAC) analyzes cancer biospecimens by mass spectrometry, characterizing and quantifying their constituent proteins, or proteome. Mass spectrometry enables highly specific identification of proteins and proteoforms, accurate relative quantitation of protein abundance in contrasting biospecimens, and the localization of post-translational protein modifications, such as phosphorylation, on a protein’s sequence.-

The CPTAC Data Portal is the centralized repository for the dissemination of proteomic data collected by the Proteome Characterization Centers (PCCs) for the CPTAC program. All data is freely available to the public, subject to the data use guidelines.

Access NCI's Surveillance, Epidemiology, and End Results (SEER) cancer databases, statistical methods, and software tools

OCG employs stringent human subjects’ protection and data access policies to protect the privacy and confidentiality of the research participants. Depending on the risk of patient identification, OCG programs’ data is available to the scientific community in two tiers: open or controlled access. Both types of data can be accessed through its corresponding OCG program-specific data matrix.

The Cancer Genome Atlas (TCGA) Data Portal provides a platform for researchers to search, download, and analyze data sets generated by TCGA. It contains clinical information, genomic characterization data, and high level sequence analysis of the tumor genomes.

It’s an ‘edge-of-your-seat’ story: The newborn’s heart had stopped multiple times in the hours since her birth. Her doctors at Lucile Packard Children’s Hospital Stanford had tried everything to help her, but her situation was dire. The baby had an unusually severe form of an inherited cardiac condition called long QT syndrome. The syndrome, which is most often diagnosed in older children or adults, can be caused by a mutation in any of several genes; until the doctors knew exactly which genetic mutation was causing the condition they wouldn’t know what drug would be most likely to help. The stakes were high: by her second day of life she’d received an implantable defibrillator and several intravenous drug infusions.

An athlete in both high school and college, Julie Prillinger had no idea anything was wrong with her until she went for a physical for a new job. The doctor detected something unusual in the rhythm of her heartbeat and referred her to a cardiologist.

Tests showed that Prillinger had an inherited condition of the heart called hypertrophic cardiomyopathy. It is caused by mutations in genes involved in the heart’s muscle cells. Those mutations typically disorganize those cells, altering the heart’s walls and disrupting the flow and force of blood out of the heart. It is the most common cause of sudden death in young people and one of the most common inherited cardiovascular disorders

Retta Beery's twins, Noah and Alexis, were born with a neurologic disorder. Through research and advocacy, Retta discovered that her twins were misdiagnosed and then, eight years later, would use whole genome sequencing to give an exact diagnosis with additional treatment that saved Noah and Alexis's lives.

The Multiple Myeloma Research Foundation (MMRF) is a charitable organization dedicated to multiple myeloma, an incurable blood cancer, which afflicts over fifty thousand Americans each year. Most medical charities focus on increasing public awareness and on raising money to distribute to researchers, in the hope that some of the work will lead to a new drug or a cure; but the MMRF runs as if it were a for-profit business, expecting high returns from the money the organization raises from donor

Founded by patients in 1986, the Lymphoma Association is a charitable organisation based in the United Kingdom that offers medical information and emotional support to lymphatic cancer patients, their families, friends and carers.