☆13May 2, 2018Updated 8 years ago
Alternatives and similar repositories for VBT-TrioAnalysis
Users that are interested in VBT-TrioAnalysis are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Divine: Prioritizing Genes for Rare Mendelian Disease in Whole Exome Sequencing Data☆13Apr 18, 2019Updated 7 years ago
- MrMosaic (Genomic Mosaic Structural Variant Caller)☆15Jul 21, 2017Updated 9 years ago
- TIDDIT - structural variant calling☆10Dec 8, 2025Updated 9 months ago
- Structural Variation breakpoint discovery via adaptive learning☆17Jul 6, 2023Updated 3 years ago
- A phenotype-based tool for variant prioritization in WES and WGS data☆41Nov 21, 2022Updated 3 years ago
- GPU virtual machines on DigitalOcean Gradient AI • AdGet to production fast with high-performance AMD and NVIDIA GPUs you can spin up in seconds. The definition of operational simplicity.
- Translocator: local realignment and global remapping enabling accurate translocation detection using single-molecule sequencing long read…☆12Jan 22, 2020Updated 6 years ago
- Support Vector Structural Variation Genotyper☆59May 29, 2020Updated 6 years ago
- Scripts and files used in the generation of the COLO829 somatic SV truthset.☆14Apr 9, 2022Updated 4 years ago
- Method for detecting STR expansions from short-read sequencing data☆63Dec 15, 2021Updated 4 years ago
- Structural variant benchmark☆24Mar 4, 2025Updated last year
- filtering trio-based genetic variants in VCFs for clinical review☆22Aug 18, 2020Updated 6 years ago
- Simulator for structural variants in various types of next-generation sequencing data☆11Mar 21, 2017Updated 9 years ago
- Simultaneous detection of SNPs and Indels using a 16-genotype probabilistic model☆27Dec 26, 2023Updated 2 years ago
- Comprehensive benchmark of structural variant callers☆49Feb 4, 2021Updated 5 years ago
- Deploy to Railway using AI coding agents - Free Credits Offer • AdUse Claude Code, Codex, OpenCode, and more. Autonomous software development now has the infrastructure to match with Railway.
- A small repo for storing the code for making the files and html for CCRs.☆22Oct 22, 2019Updated 6 years ago
- GENetic Effect-Size distribution Inference from Summary-level data☆16Sep 6, 2020Updated 6 years ago
- ☆20Mar 31, 2021Updated 5 years ago
- MUltiScale enrIchment Calling for ChIP-Seq Datasets☆23Mar 14, 2019Updated 7 years ago
- ☆55Jun 24, 2020Updated 6 years ago
- Workflows used for WGS data processing -- replaced by https://github.com/gatk-workflows/gatk4-genome-processing-pipeline☆57Jan 24, 2020Updated 6 years ago
- Detects human contamination in bam files☆16Sep 10, 2020Updated 6 years ago
- ☆14Jul 14, 2026Updated 2 months ago
- ☆13Jun 21, 2017Updated 9 years ago
- End-to-end encrypted email - Proton Mail • AdSpecial offer: 40% Off Yearly / 80% Off First Month. All Proton services are open source and independently audited for security.
- Data and information about the Polaris study☆56Nov 18, 2019Updated 6 years ago
- Evaluate variant calls and its combination with k-mer multiplicity☆73Dec 2, 2022Updated 3 years ago
- A tool to analyze telomeric reads from WGS or telobait-capture long-read sequencing data☆10Oct 1, 2024Updated last year
- Calling deletions using deep convolutional neural☆26Feb 12, 2020Updated 6 years ago
- HAT is a set of tools for calling de novo variants from whole-genome sequencing data.☆24Nov 18, 2025Updated 10 months ago
- ☆15Aug 22, 2023Updated 3 years ago
- Polygenic score calculation from VCF in Nim.☆15Nov 22, 2020Updated 5 years ago
- A simple observation count database☆11Sep 10, 2026Updated last week
- Fast and scalable variant annotation tool☆30May 1, 2022Updated 4 years ago
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- Call regions of homozygosity and make tentative UPD calls☆12Jun 27, 2025Updated last year
- hail-based pipelines for annotating variant callsets and exporting them to clickhouse☆23Aug 6, 2026Updated last month
- VIPER (Variant InsPector and Expert Rating tool) can be utilised to view variant calls and decide whether or not those are true or false …☆16Jan 17, 2022Updated 4 years ago
- The integrated pipeline for Indel detection☆17Apr 29, 2018Updated 8 years ago
- ☆16Jan 10, 2022Updated 4 years ago
- DNN-based small variant caller☆12May 2, 2022Updated 4 years ago
- A nextflow pipeline for analysing expression and splicing in RNA seq data from rare disease patient☆19Updated this week