![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
Data Analysis for Genomics, free HarvardX course, starts April 7 | Michael Love | Bioinformatics | 8 | 12-16-2014 06:27 AM |
reference-free SNP discovery | Marius | De novo discovery | 5 | 03-30-2011 12:23 PM |
PubMed: Reference-free validation of short read data. | Newsbot! | Literature Watch | 0 | 02-22-2011 12:00 PM |
Reference-Free Validation of Short Read Data | krobison | Literature Watch | 1 | 09-23-2010 05:40 PM |
![]() |
|
Thread Tools |
![]() |
#1 |
Registered Vendor
Location: San Francisco, CA Join Date: Mar 2014
Posts: 18
|
![]()
In order to accelerate our understanding of the molecular basis of diseases such as cancer, it is imperative for the research community to be able to work with large cohorts of patient-derived genomics data generated by consortium efforts like The Cancer Genome Atlas (TCGA) and the Genotype Tissue Expression (GTEx) Project.
Station X is making it free & easy to rapidly mine large cohorts of patient-derived genomics data. GenePool Reference™ is a free and growing resource where human genomics data tied to corresponding clinical metadata is available for analysis and interpretation. Simply register free-of-charge (http://www.stationxinc.com/) and get access to: * 7,000+ samples worth of whole genomes, exomes, targeted sequencing panels, and transcriptomes including TCGA and GTEx projects, with more on the way driven by user requests * Associated clinical metadata such as demographic, treatment, recurrence, and other features * Built-in, best-in-class analysis & statistical tools such as profiling, comparison, time-to-endpoint, co-expression networks, gene-set enrichment, and clustering * Interactive visualizations * Built-in, dynamic annotations For more information about GenePool Reference™ and the various genomics cohorts available, please click here (http://www.stationxinc.com/reference-library). If you are interested in using GenePool with your own genomics data, simply check out http://www.stationxinc.com to find out how. GenePool is Station X’s software environment for the management, analysis and sharing of cohort-scale genomics data. GenePool makes it easy for translational and clinical researchers to make sense of mutation and expression data derived from sequencing platforms. Last edited by GenePool; 11-22-2014 at 12:16 AM. |
![]() |
![]() |
![]() |
#2 |
Registered Vendor
Location: San Francisco, CA Join Date: Mar 2014
Posts: 18
|
![]()
Station X has recently made The Cancer Genome Atlas comprehensively available instantly for users of GenePool.
GenePool now provides instant access to the following TCGA assays: *Somatic Mutations (per patient derived from exome sequencing of Tumor and matched Blood-Normal sample) *RNA-Seq (genes, isoforms, exons, splice junctions) *miRNA-Seq *Protein Expression (array-based) *DNA Methylation (chip-based) *Copy Number (chip-based) Check out the following SeqAnswers thread for more information: http://seqanswers.com/forums/showthread.php?t=48485 ------------------------------ GenePool is making genomics data management, analysis, and sharing easier! Products @ www.stationxinc.com Last edited by GenePool; 11-23-2014 at 09:27 PM. |
![]() |
![]() |
![]() |
Tags |
analysis software, biomarkers, exome, genome annotation, rna-seq |
Thread Tools | |
|
|