fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing
-
Updated
Jul 12, 2024 - Nim
fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing
🔅 State manager for deeply nested states
A Tool to Annotate and Prioritize Exome Variants
Please consider using/contributing to https://github.com/nf-core/sarek
WES HLA Typing based on multiple alternative tools
Target exome sequencing analysis for NYU NGS580 gene panel
eXome Hidden Markov model (XHMM) - Copy Number Variants (CNVs) from Whole Exome Sequencing Data
MEM : Mendelian Error Method to rapidly detect deletions in whole exome and genome trio sequence data
Exome Slicer - Application to evaluate sequencing quality when designing an Exome Slice (NGS virtual panel)
Cloud based analysis for Doctors, Researchers, Bioinformaticians and Developers.
Variantes genéticas de amostras de Rattus norvegicus utilizando GATK4
COverage Analysis Tool have been developed in 2016. It aims to automatically find bad quality regions of coding sequences in a set of sequencing data. It includes a graphical interface.
Add a description, image, and links to the exome topic page so that developers can more easily learn about it.
To associate your repository with the exome topic, visit your repo's landing page and select "manage topics."