Difference between revisions of "MMSEQ"

From UFRC
Jump to navigation Jump to search
m (Text replacement - "#uppercase" to "uc")
Line 33: Line 33:
 
-->
 
-->
 
==System Variables==
 
==System Variables==
* HPC_{{#uppercase:{{#var:app}}}}_DIR
+
* HPC_{{uc:{{#var:app}}}}_DIR
 
<!--Configuration-->
 
<!--Configuration-->
 
{{#if: {{#var: conf}}|==Configuration==
 
{{#if: {{#var: conf}}|==Configuration==

Revision as of 21:21, 6 December 2019

Description

mmseq website  

The MMSEQ package contains a collection of statistical tools for analysing RNA-seq expression data. Expression levels are inferred for each transcript using the mmseq program by modelling mappings of reads or read pairs (fragments) to sets of transcripts. These transcripts can be based on reference, custom or haplotype-specific sequences. The latter allows haplotype-specific analysis, which is useful in studies of allelic imbalance. The posterior distributions of the expression parameters for groups of transcripts belonging to the same gene are aggregated to provide gene-level expression estimates. Other aggregations (e.g. of transcripts sharing the same UTRs) are also possible. Isoform usage (i.e., the proportion of a gene's expression due to each isoform) is also estimated. Uncertainty in expression levels is summarised as the standard deviation of the posterior distribution of each expression parameter. When the uncertainty is large in all samples, a collapsing algorithm can be used for grouping transcripts into inferential units with reduced levels of uncertainty.

Required Modules

Serial

  • mmseq

System Variables

  • HPC_MMSEQ_DIR





Validation

  • Validated 4/5/2018