Multi-nucleotide Variation Annotation Corrector
☆11Dec 13, 2022Updated 3 years ago
Alternatives and similar repositories for MAC
Users that are interested in MAC are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Somatic workflow for Kids-First☆15Mar 13, 2026Updated last week
- Multi-nucleotide variants (MNVs) in gnomAD 2.1☆12Feb 27, 2026Updated 3 weeks ago
- Method to detect exonic CNVs in NGS Gene Targeted Panels☆16Dec 3, 2019Updated 6 years ago
- Mutational signature analysis for low statistics SNV data☆64Aug 7, 2024Updated last year
- Platypus Variant Caller☆108Jun 27, 2024Updated last year
- Managed Database hosting by DigitalOcean • AdPostgreSQL, MySQL, MongoDB, Kafka, Valkey, and OpenSearch available. Automatically scale up storage and focus on building your apps.
- ☆36Mar 16, 2021Updated 5 years ago
- Python scripts for matching output of Pacific Biosciences IsoSeq RNA-seq pipeline to an annotation file.☆23Sep 24, 2015Updated 10 years ago
- A standalone end-to-end data analysis pipeline for Duplex Sequencing☆21Oct 25, 2023Updated 2 years ago
- ☆13Dec 3, 2018Updated 7 years ago
- ☆13Oct 14, 2017Updated 8 years ago
- Browser-based tool for visualizing and analyzing germline copy number variants in genomic data