Call and score variants from WGS/WES of rare disease patients.
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Updated
Nov 1, 2024 - Nextflow
Call and score variants from WGS/WES of rare disease patients.
cfDNApipe: A comprehensive quality control and analysis pipeline for cell-free DNA high-throughput sequencing data
Generic human DNA variant annotation pipeline
Data management of large-scale whole-genome sequence variant calls (Development version only)
xGAP is an efficient, modular, extensible and fault-tolerant pipeline for massively parallelized genomic analysis/variant discovery from next-generation DNA sequencing data.
Multi-bAse Codon-Associated variant Re-annotatiON (MACARON)
acorn is an R package that examines various features of de novo variants including subsetting DNVs by individual, variant type, or genomic region; calculating features including variant change counts, lengths, and presence/absence at CpG sites; and characteristics of parental age and number of DNVs.
A collection of software to work with genomic variants
Predictive marker discovery for groups; binary data, genomic data (single nucleotide variants), arbitrary character data.
🌳 Human ancestry inference from genomic data
Pipeline for gene candidate discovery based on mutagenesis. Featured in gene cloning research published in Nature (DOIs: 10.1038/s41467-020-14937-2, 10.1038/s41467-021-23738-0, 10.1038/s41477-021-00971-5), Molecular Plant (DOI: 10.1016/j.molp.2021.05.010) and New Phytologist (DOI: 10.1111/nph.17075).
Estimates the clonal population structure in a tumour sample given a cell mutation matrix
Pipeline to call SNV's with 4 tools (VarDict, LoFreq, Mutect2 & SiNVICT)
Extract and explore snv data
Genome assembly and variant benchmarks for Chinese Quartet
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