Galaxy is an open source, web-based platform for data intensive biomedical research. If you are new to Galaxy start here or consult our help resources. You can install your own Galaxy by …

Galaxy is a community-driven web-based analysis platform for life science research.

For the specifics of using the RNA-seq tools already wrapped for Galaxy, the top of the Galaxy Support wiki has links to many resources. The NGS 101 has an RNA-seq example and the …

HISAT2 usage is covered in the Galaxy RNA-seq tutorials: https://galaxyproject.org/learn/ RNA-seq: Introduction - an introductory tutorial for transcriptome analysis. …

Hi, I have RNA-Seq data and want to analyze lncRNA, SNV, and SNP from this data through Galaxy. How I will do this please anyone helps me in this regard. Anshul

Hello, I'm new in NGS and i'm currently working on RNA-seq. I had 6G of illumina reads and proceed with the data processing. After joining my paired end reads into a single file, I ran …

Hello, Currently, RNA-seq analysis for SOLiD data is available only on our test server: http://test.g2.bx.psu.edu/ Please note that there are quotas associated with the test server: …

Most of Galaxy's mapping tools have this option, although it may be named slightly differently on the tool forms. A double check that your uploaded reference genome has the same exact …

Data from other sources can be loaded into Galaxy and used with many tools. The Galaxy 101 (found in the tutorial's link above) has examples of retrieving, grouping, joining, and filtering …

Oct 20, 2017 · I am new to RNAseq data and learning this process step by step, so I have a few questions (I highlighted the questions below, so they are easily visible after reading the whole …