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Search results for snv
snv
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17 search results found
Pcgr
⭐
234
Personal Cancer Genome Reporter (PCGR)
Strelka
⭐
204
Strelka2 germline and somatic small variant caller
Lancet
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145
Microassembly based somatic variant caller for NGS data
Raredisease
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64
Call and score variants from WGS/WES of rare disease patients.
Bayestyper
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52
A method for variant graph genotyping based on exact alignment of k-mers
Monopogen
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50
SNV calling from single cell sequencing
Gvanno
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43
Generic human DNA variant annotation pipeline
Platinumgenomes
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42
The Platinum Genomes Truthset
Clairs
⭐
42
ClairS - a deep-learning method for long-read somatic small variant calling
Seqarray
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41
Data management of large-scale whole-genome sequence variant calls (Development version only)
Cfdnapipe
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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
Igda
⭐
10
Detect and phase minor SNVs from long-read sequencing data
Pyreqtl
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9
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.
Dockstore Cgpwgs
⭐
9
Dockstore implementation of CGP core WGS analysis
Snvphyl_nextflow
⭐
7
Nextflow version of SNVPhyl
Fings
⭐
6
Filters for Next Generation Sequencing
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1-17 of 17 search results
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