zavolanlab/PAQR2

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Python
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GNU General Publi...
Created about 3 years ago
Updated almost 2 years ago

zavolanlab/PAQR2

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Updated version of PAQR, which was previously available in the PAQR_KAPAC joint repository.

zarp

The Zavolab Automated RNA-seq Pipeline

htsinfer

Infer metadata for your downstream analysis straight from your RNA-seq data

polyAsite_workflow

Pipeline for the processing of 3' end sequencing libraries

Dockerfiles

Dockerfile repository of the Zavolan Lab

PAQR_KAPAC

scripts, pipelines and documentation to run PAQR and KAPAC; KAPAC allows to infer regulatory sequence motifs implicated in 3’ end processing changes; PAQR enables the quantification of poly(A) site usage from standard RNA-seq data

TECtool

TECtool uses mRNA and 3’ end sequencing data to identify novel terminal exons.

RCRUNCH

Workflow for automated (e)CLIP analysis. From raw fastq to peak calling and motif analysis.

bindz-rbp

RBP module for bindz, a bioinformatics tool to detect regulators' binding sites on RNA sequences.

MIRZAG

MIRZA-G - Pipeline and model for miRNA target prediction

zarp-cli

A user-friendly command-line interface for the ZARP RNA-seq analysis workflow

programming-for-life-sciences

Toy repository for the Programming for Life Sciences course at the Biozentrum, University of Basel

mirflowz

Snakemake workflow for the mapping and quantification of miRNAs and isomiRs from miRNA-Seq libraries.

SCUREL

Method to detect 3'UTR changes from scRNA-seq

snoRNAHybridSearchPipeline

A pipeline to discover snoRNA-target chimeric reads in CLIP/HTS experiments.

SCINPAS

Single Cell Identification of Novel PolyA Sites.

CWL_repository

Zavolan-Lab repository for CWL Tools and Workflows

Common Workflow Language

tandem-pas

Extract set of tandem poly(A) sites from the PolyASite atlas.

srsf1_selex_Allain_lab

Notebook of SELEX data analysis

Jupyter Notebook

scRNAsim-toolz

A repository for the tools used by scRNAsim.

multiqc-plugins

Custom plugins for the MultiQC tool.

zpca

bindz-service

tin-score-calculation

Given a set of BAM files and a gene annotation BED file, calculates the Transcript Integrity Number (TIN) for each transcript.