Repository bayesase
Name: bayesase
Owner: malex
Synopsis: Bayesian analysis of allele specific expression.
It's a flexible and very general implementation of a Bayesian approach to estimating Allelic
Imbalance (AI) and formally comparing levels of AI between conditions. Allelic imbalance (AI)
indicates the presence of functional variation in cis regulatory regions. Detecting cis
regulatory differences using AI is widespread, yet there is no formal statistical methodology
that tests whether AI differs between conditions. The testing for AI involves several complex
bioinformatics steps. BayesASE is a complete bioinformatics pipeline that incorporates
state-of-the-art error reduction techniques and a flexible Bayesian approach to estimating AI
and formally comparing levels of AI between
conditions (https://www.g3journal.org/content/8/2/447.long).
Type: unrestricted
Revision: 0:8b2027117ce5
This revision can be installed: True
Times cloned / installed: 158

Contents of this repository

Name Description Version Minimum Galaxy Version
merges filtered/summarized ASE Counts tables to the Calculated Prior values 21.1.13 16.01
for one condition to test for Allelic Imbalance 21.1.13 16.01
sum technical replicates 21.1.13 16.01
- check read numbers in and out of Compare SAM Files and Create ASE Counts Tables tool 21.1.13 16.01
for Bayesian Analysis of Allelic Imbalance 21.1.13 16.01
that do not overlap with genic features for BayesASE (using awk) 21.1.13 16.01
for correct formatting and duplicate FASTQ names 21.1.13 16.01
containing read counts for each parental genome 21.1.13 16.01
using ASE Count Tables 21.1.13 16.01
for use in BayesASE Align and Count workflow 21.1.13 16.01
verify starting FASTQ read number equals read number after running BWASplitSAM tool 21.1.13 16.01
with awk 21.1.13 16.01
for correct formatting and header names 21.1.13 16.01
creates a SAM file of uniquely mapping reads from a BWA-MEM alignment 21.1.13 16.01
based on user-defined APN threshold 21.1.13 16.01
verify 2 SAM files are present for every 1 FASTQ file. 21.1.13 16.01
with features of interest in RNAME field 21.1.13 16.01
nbmodel_stan2_flex_prior.R 21.1.13 16.01
converts a SAM file to a BED file for use in BayesASE 21.1.13 16.01
for use in Calculate Priors Module for BayesASE 21.1.13 16.01

Categories
Transcriptomics - Tools for use in the study of Transcriptomics.