There are 0 repository under fastqc topic.
An interactive web tool for quality control of DNA sequencing data
A (very) fast program for getting statistics about a fastq file, the way I need them, written in Rust
RNA-seq pipeline for raw sequence alignment and transcript/gene quantification.
FAstqc DAta PArser - A minimal parser to parse FastQC output data.
Here we are going to discuss variant calling on human datasets using GATK Best practices pipeline
A simple fastp-MultiQC nextflow pipeline
Quality Control, Mapping and Reads Count for RNA-Seq Analysis
Analysis pipeline for processing paired-end Illumina reads obtained after ancient mtDNA target enrichment capture.
Qiime2 and DADA2 are one of the latest bioinformatics tools used in 16S RNA analysis. The current Qiime2 and DADA2 pipelines support End to End 16S RNA analysis, among other analyses.
Estimate fastq-formatted read abundace in RNA-Seq analysis with Kallisto
Python code to compute adatper content in reads, kmer content, per-base-GC content (at a specific position in a read alignment, against reference genome), per base NC content (at a specific position in a read alignment against the reference genome), per base seq quality (across aligned reads), per base sequence content, per base quality scores, per tile sequence quality
Whole Exome Sequencing end-to-end pipeline. Starting from whole exome fastq files: Data QC, Adapter Trimming, Reference Genome Alignment, SAM/BAM Validation, Data Recalibration and Variant Calling.
Map and post-process your bams for SNP calling
血小板转录组fastq数据处理
This is a code tutorial for rna or dna sequence mapping by myself-RyanYip
A Snakemake Workflow for using PolyA_DB and UCSC LiftOver with CellRanger
Complete Pipeline for RNA-seq data analysis: From FastQ to differntial gene expression to annotated Variations.
A Snakemake workflow for quality control assessment of Illumina NGS data using FastQC and MultiQC
Bulk Rna-seq Analysis
A workflow automation script: demultiplex the library sequence, run quality checks, deliver to archiving and processing afterwards
Snakemake workflow for Salmon quantification and FastQC quality controls
Slurm scripts for analyzing bulk Cutandtag data
Tools to analyze fasta or fastaq files with python.
The repository contain directories of projects done during the bioinformatics degree program
Genomic Analysis Pipeline: Automate data preprocessing, variant calling, and annotation with Snakemake. Ensure reproducibility and reliability in genomic studies.
A script that efficiently processes multiple '.fastq' files, automatically organizing the pre-trimmed output into a folder named 'qc_reports_pretrim' for streamlined quality control and sequence data analysis.
Exploring Bioinformatics pipelines
Walks through installation and usage of FASTQC, MultiQC, Trimmomatic, and Salmon for transcriptomic data preprocessing. Includes Grid Engine shell scripts that can be looped over many files in a directory.
Build Docker container for FastQC software and (optionally) convert to Apptainer/Singularity.