Pediatric Cancer Genome Project | Explore hosts data and tools from Pediatric Cancer research done at St. Jude Children's Research Hospital in collaboration with Washington University School of Medicine in St. Louis.
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St. Jude Children's Research
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Pediatric Cancer Genome Project | Explore - St. Jude Children's Research Hospital, Washington University School of Medicine in St. Louis | pcgpexplore.org Reviews
https://pcgpexplore.org
Pediatric Cancer Genome Project | Explore hosts data and tools from Pediatric Cancer research done at St. Jude Children's Research Hospital in collaboration with Washington University School of Medicine in St. Louis.
pcgpexplore.org
Gene Expression - Pediatric Cancer Genome Project | Explore
http://www.pcgpexplore.org/geneExpression;jsessionid=C3929EFDFDA8498186494075B7A7A413
Pediatric Cancer Genome Project. PCGP Germline Variant Search. Raw Data Access Form. Enter Gene Symbol or Probe Set ID. By Copy Number Change. T-ALL vs. ETP. St Jude Children's Research Hospital and Washington University School of Medicine in St. Louis. Raw Data Access Form. PCGP Explore - What's New. Released the Rhabdosarcoma(RHB) study results. Added the mRNA Accession number to the SNV-Indel Tier 1 data chart. Click here to view Release Notes. There was an error processing your request.
APIs - Pediatric Cancer Genome Project | Explore
http://www.pcgpexplore.org/apis;jsessionid=C3929EFDFDA8498186494075B7A7A413
Pediatric Cancer Genome Project. PCGP Germline Variant Search. Raw Data Access Form. We are currently offering a beta version of an application programming interface for R ( http:/ www.r-project.org. Which can be installed using the instruction below. Script to install PCGP packages [PCGPDataAPI version 0.4 (beta version)]. To install a particular package, e.g., PCGPDataAPI, type (or copy and paste) the following in an R command window. Get all structural variants for all patients. Par (mfcol=c(1,2) ;.
Pediatric Cancer Genome Project | Explore
http://www.pcgpexplore.org/dataAccess;jsessionid=C3929EFDFDA8498186494075B7A7A413
Pediatric Cancer Genome Project. PCGP Germline Variant Search. Raw Data Access Form. Raw Data Access Form. Please refer to the Guidelines and Information. For further information and for details on how to apply for access to the data. For access to the data should be completed and submitted using the Fax or the Email Address stated below. Applications will only be accepted electronically in PDF format. Please print out the Application Form. Raw Data Access Form. PCGP Explore - What's New.
About - Pediatric Cancer Genome Project | Explore
http://www.pcgpexplore.org/about;jsessionid=C3929EFDFDA8498186494075B7A7A413
Pediatric Cancer Genome Project. PCGP Germline Variant Search. Raw Data Access Form. The goals of the Explore data dashboard of the Pediatric Cancer Genome Project are:. To facilitate access to high-quality genomic data for pediatric cancers. To accelerate discovery and hypothesis testing. To provide comprehensive visualizations of the data. To contribute to the elucidation and understanding of the fundamental processes underlying pediatric cancers. Internet Explorer 8.0 , Mozilla Firefox 3.5 ,.
Analysis - Pediatric Cancer Genome Project | Explore
http://www.pcgpexplore.org/analysis;jsessionid=C3929EFDFDA8498186494075B7A7A413
Pediatric Cancer Genome Project. PCGP Germline Variant Search. Raw Data Access Form. CNV - Number of Overlapping Genes. Filter by Pathway Group. Deletion, Insertion, Inversion. Click on the 'Pathway, Gene Symbol or % Alt (% Alterations)' column headings to sort the data. The % alteration for each Gene Symbol is calculated by identifying affected patients over total patients displayed in the matrix plot. St Jude Children's Research Hospital and Washington University School of Medicine in St. Louis.
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Pediatric Cancer Genome Project | Explore - St. Jude Children's Research Hospital, Washington University School of Medicine in St. Louis
Pediatric Cancer Genome Project. PCGP Germline Variant Search. Raw Data Access Form. Number of Discovery (WGS) Patients/Sequences by Disease. Sequence and Analysis Completed (378): (378, 57.52%). Public (152): (152, 23.15%). Published (128): (128, 19.48%). Public" data-link="https:/ www.ebi.ac.uk/ega/datasets/EGAD00001000135". NBL (42, 6.39%). Public" data-link="https:/ www.ebi.ac.uk/ega/datasets/EGAD00001000160". ACT (8, 1.22%). EPD (22, 3.35%). PHALL (9, 1.37%). INF (22, 3.35%). HGG (15, 2.28%). Sequen...
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