Clinical Whole Genome and Exome Sequencing Pipeline
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Updated
Jan 21, 2025 - Python
Clinical Whole Genome and Exome Sequencing Pipeline
🐳 Dockerized WES pipeline for variants identification in mathced tumor-normal samples
An open-source and scalable solution to NGS analysis powered by the NIH's Biowulf cluster.
Map and post-process your bams for SNP calling
STAR-NN: A deep neural network model to predict the risk of ASD using whole exome sequencing dataset
An adaptable method for analyzing SNVs, INDELs, and CNVs from Whole Exome Sequencing (WES) data, emphasizing germline variants.
An automated tool for processing whole-exome sequencing data
WES pipeline with customizable scoring system based on 10 criteria.
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