miscellaneous stand-alone basic utilities for genomics and genomics-adjacent operations (share with lab mates)
-
Updated
Sep 11, 2025 - Python
miscellaneous stand-alone basic utilities for genomics and genomics-adjacent operations (share with lab mates)
Pipeline para montagem direcionada (gene-a-gene) a partir de leituras pareadas.
This repository covers research paper implementations in the field of Genomics, Next Generation Sequencing, Bioinformatics and Machine Learning.
This project plots the effect of selecting different kmer length parameter in 2 different de novo genome assembly tools - AbySS and Velvet.
Coverage graph creator from BAM files (included in the SSV-Conta package)
Coverage graph creator from BAM files (included in the SSV-Conta package)
Python scripts for design of 5'/3' RACE-based NGS panels, and the following data analysis
Bioinformatics is a field of information technology and biological science, which use to managing, storing and analyzing these biological data such as DNA, RNA and protein, In this repository I'm use python to create various types of program for analyzing biological data
Metrics App is a bioinformatics application developed in Python and Streamlit for calculate Depth of Coverage and Breadth of Coverage from BAM/CRAM files.
Professional MCP server for FastQC and MultiQC quality control analysis with advanced visualization and report parsing
CRISPRSeqSim is a tool that simulates results of CRISPR/cas editing fragments target sequencing.
A tool to calculate the equipolar amounts of two amplicons for upcoming sequencing with NGS
Clinical Prediction tool with inbuild machine learning model
Files pertaining to the processing of NGS data in .fasta.gz format for the purposes of identifying the genomic sequences which belong to either of the tuataras dual mitochondrial genomes.
Custom scripts and workflows used in the genomics and population analysis of oat crown rust (Puccinia coronata f. sp. avenae) preprint (bioRxiv 2023.09.18.557855). All steps performed in Linux environment or R.
various tools that help with deep sequencing analysis
Snakemake pipeline to merge gnomAD VCF files
Add a description, image, and links to the ngs-analysis topic page so that developers can more easily learn about it.
To associate your repository with the ngs-analysis topic, visit your repo's landing page and select "manage topics."