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Search results for python snv

2 search results found

Monopogen ⭐ 50

SNV calling from single cell sequencing

Generic human DNA variant annotation pipeline

ClairS - a deep-learning method for long-read somatic small variant calling

Cfdnapipe ⭐ 24

cfDNApipe: A comprehensive quality control and analysis pipeline for cell-free DNA high-throughput sequencing data

Clairs To ⭐ 18

ClairS-TO - a deep-learning method for tumor-only somatic SNV calling

A collection of Python modules equivalent to R ReQTL Toolkit aims to identify the association between expressed SNVs with their gene expression using RNA-sequencing data.

Filters for Next Generation Sequencing

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