There are 0 repository under bowtie2 topic.
Detecting contamination in NGS data and multi-species analysis
Here we are going to discuss variant calling on human datasets using GATK Best practices pipeline
Snakemake pipeline for Popoolation and Popoolation2
Align short RNA seqeuncing reads to determine the length of of overhang
🦠Course project in Bioinformatics Institute 2023-2024
Panlineal is capable of generating Vgs from multiple genome alignments in form of lineal pan-genome. Combining short reads data, it can also detect the the allelism conduced by PAVs combinations of vast samples in a species.
Some scripts to make your bioinformatics analyses reproducible and a bit easy 🤓
A pipeline to run mapping, mash screen and assembly methods for pATLAS.
This is a code tutorial for rna or dna sequence mapping by myself-RyanYip
Script to obtain plasmid id from WGS data using bowtie2 to map
Slurm scripts for analyzing bulk Cutandtag data
The repository contain directories of projects done during the bioinformatics degree program
This is a repository for a seminar on Bowtie2 and its use of the Burrows-Wheeler Transform and FM-index in short-read sequence mapping.
This project explores the PBRM1-PIAS1 interaction in epithelial differentiation through ChIP-seq analysis, highlighting EZH2's role and implications for cholesterol biosynthesis in cellular processes.
Bowtie2 v2.5.2 Dockerfile Native for Apple M1+ Silicon (ARM64) and Intel/AMD (x86_64) Containers
Align reads over a reference genome, filter aligned-reads, and mark duplicates
Snakemake workflow used to call peaks with Macs2
RNA-seq code with Bowtie alignment and generating strain-specific counts using Emase
Build Docker container for Bowtie 2 and (optionally) convert to Apptainer/Singularity.
Sequencing data preprocessing