A genome annotation pipeline that use short and long sequencing reads alignments from animal genomes
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Updated
Apr 10, 2024 - Nextflow
A genome annotation pipeline that use short and long sequencing reads alignments from animal genomes
RNA-seq pipeline for raw sequence alignment and transcript/gene quantification.
These are tutorials on a subset of tools available for processing raw RNAseq data. This if for HISAT2_SAMtools_Stringtie_gffcompare_ballgown pipeline or HISAT2_SAMtools_Stringtie_PrepDEanalysis.py_DESeq2 pipeline
This repository houses the pipeline I coded to perform differential analysis of transcriptomes from two oyster species, C. gigas and C. virginica and isolate genes in the apoptosis pathway.
Attempt at snakemake pipeline. Pyflow was forked from https://github.com/crazyhottom but the Snakefile infrastructure and rule calling was inspired by https://github.com/snakemake-workflows
snakemake files of the tuxedo v2 pipeline from Pertea et al 2016
This project uses an workflow pipeline to generate map and assemble RNAseq reads to a reference genome. Furthermore, we generate counts data and identify differentially expressed genes from 2 conditions.
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