A tool to detect postzygotic single-nucleotide mosaicism from unpaired, trio, or paired samples.
☆13Feb 23, 2021Updated 5 years ago
Alternatives and similar repositories for MosaicHunter
Users that are interested in MosaicHunter are comparing it to the libraries listed below
Sorting:
- MrMosaic (Genomic Mosaic Structural Variant Caller)☆15Jul 21, 2017Updated 8 years ago
- ☆25Apr 29, 2018Updated 7 years ago
- VCF files of SVs using long-read sequencing (LRS).☆22Dec 17, 2021Updated 4 years ago
- R htmlwidget package for ideogram.js☆15Oct 26, 2022Updated 3 years ago
- dv-trio provides a pipeline to call variants for a trio (father-mother-child) using DeepVariants [1]. Genomic Variant Calling Files (gVCF…☆11Feb 3, 2021Updated 5 years ago
- A mosaic detecting software based on phasing and random forest☆70Dec 8, 2025Updated 3 months ago
- Allele frequency filtering for Mendelian variant discovery☆18Sep 27, 2016Updated 9 years ago
- An R package to detect, classify, and visualize genome rearrangements☆15Aug 4, 2020Updated 5 years ago
- Plot CNV data with a genome viewer in R☆15Apr 5, 2017Updated 8 years ago
- Seeking information like heteroplasmy, structure variants, etc. on Mitochondrial genome from next generation sequencing☆41Dec 11, 2018Updated 7 years ago
- ☆15Jan 10, 2023Updated 3 years ago
- RCK: Reconstruction of clone- and haplotype-specific Cancer Karyotypes☆18Apr 2, 2020Updated 5 years ago
- ☆14Dec 13, 2023Updated 2 years ago
- VariantStore: A Large-Scale Genomic Variant Search Index☆39Jul 9, 2021Updated 4 years ago
- ☆23Nov 9, 2025Updated 3 months ago
- ☆20Nov 30, 2023Updated 2 years ago
- MOsaic CHromosomal Alterations (MoChA) caller☆92Aug 22, 2025Updated 6 months ago
- genome basic statistics tool (e.g. n50, n10, ng50,...)☆15Mar 5, 2012Updated 14 years ago
- Divine: Prioritizing Genes for Rare Mendelian Disease in Whole Exome Sequencing Data☆13Apr 18, 2019Updated 6 years ago
- ☆23Feb 16, 2026Updated 2 weeks ago
- Interface to various variant calling formats.☆31Jun 15, 2024Updated last year
- Mutational Signature Comprehensive Analysis Toolkit☆15Feb 19, 2026Updated 2 weeks ago
- ☆10Jun 9, 2020Updated 5 years ago
- WGS Pipeline☆13Jan 19, 2018Updated 8 years ago
- Ontoclick - A web browser extension to turn highlighted text into a proper Ontology term.☆13Jun 2, 2023Updated 2 years ago
- Nanopanel2: a somatic variant caller for Nanopore panel sequencing data☆11Sep 21, 2021Updated 4 years ago
- Pan gGnome Viewer☆10Jul 10, 2025Updated 7 months ago
- Post variant-calling QC pipeline for orienting cohort data with a reference file. Additional steps for merging and phasing with a referen…☆11Jun 10, 2019Updated 6 years ago
- Open Targets Genetics UI☆15Jan 31, 2025Updated last year
- Fast in-silico normalization algorithm for NGS data☆23Nov 1, 2021Updated 4 years ago
- ☆26Aug 10, 2021Updated 4 years ago
- HaploGrep - mtDNA haplogroup classification. Supporting rCRS and RSRS.☆78Feb 28, 2023Updated 3 years ago
- CNV calling algorithm for detection of homozygous and hemizygous deletions from whole exome sequencing data☆12Nov 9, 2025Updated 3 months ago
- SeqOthello supports fast coverage query and containment query.☆12May 8, 2019Updated 6 years ago
- ☆14Oct 29, 2021Updated 4 years ago
- Altered TCR Ligand Affinities and Structures☆12Dec 1, 2023Updated 2 years ago
- ☆13May 2, 2018Updated 7 years ago
- Pipeline for Illumina shotgun sequencing of 16S rRNA amplicon sequences☆14Sep 2, 2016Updated 9 years ago
- Haplotype-based somatic genome simulator☆10May 19, 2017Updated 8 years ago