☆29Feb 17, 2021Updated 5 years ago
Alternatives and similar repositories for smart-variant-filtering
Users that are interested in smart-variant-filtering are comparing it to the libraries listed below
Sorting:
- Generate an enhanced VCF files from ClinVar XML Full releases☆15Feb 23, 2026Updated last week
- Integrated Variant Caller☆17Mar 15, 2018Updated 7 years ago
- VVP (VAAST Variant Prioritizer) rapidly prioritizes genetic variants☆19Mar 10, 2018Updated 7 years ago
- Ximmer is a system for CNV calling on exome and targeted genomic sequencing☆19Jan 28, 2026Updated last month
- BigWig manpulation tools using libBigWig and htslib☆30Aug 8, 2024Updated last year
- GARFIELD-NGS: Genomic vARiants FIltering by dEep Learning moDels in NGS☆17Mar 4, 2019Updated 7 years ago
- iAnnotateSV is a Python library and command-line software toolkit to annotate and visualize structural variants detected from Next Genera…☆16Dec 31, 2025Updated 2 months ago
- Ultra Fast NGS Data QC Tool☆28Feb 14, 2021Updated 5 years ago
- SiNVICT: Ultra-Sensitive Detection of Single Nucleotide Variants and Indels in Circulating Tumour DNA☆27Oct 6, 2020Updated 5 years ago
- A nextflow pipeline for calling exome CNVs☆13Feb 24, 2026Updated last week
- A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data