A comprehensive and standardized approach for transcriptomic profiling as a clinically-oriented application. |
hg clone https://toolshed.g2.bx.psu.edu/repos/bioitcore/transcriptomics_easy_for_discovery_toolkit
Name | Description | Version | Minimum Galaxy Version |
---|---|---|---|
Unfold columns from a table | 0.0.1 | 16.01 | |
1.0.0 | 16.01 | ||
- Drugbank Genetic Variants | 1.0.0 | 16.01 | |
Join Intervals on Reference Alternative Splicing Events | 1.0.0 | 16.01 | |
- Dividing numeric values by 2 | 1.0.0 | 16.01 | |
- Multiplying numeric values by 2 | 1.0.0 | 16.01 | |
1.0.0 | 16.01 | ||
A statistic tool for quantifying exon inclusion ratios in paired-end RNA-seq data, with broad applications for the study of alternative splicing. | 1.0.0 | 16.01 | |
Join Intervals on Reference Transcipts | 1.0.0 | 16.01 | |
A tool for identifying chimeric transcription in sequencing data. | 1.0.0 | 16.01 |