An insertion caller for Illumina paired-end WGS data.
☆26Aug 22, 2025Updated last year
Alternatives and similar repositories for INSurVeyor
Users that are interested in INSurVeyor are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- HAT is a set of tools for calling de novo variants from whole-genome sequencing data.☆24Nov 18, 2025Updated 11 months ago
- Ultra-efficient mapping-free structural variation genotyper☆20Jul 28, 2021Updated 5 years ago
- Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat☆42Apr 22, 2026Updated 5 months ago
- Population-scale detection of non-reference sequence variants using colored de Bruijn Graphs☆27Apr 29, 2024Updated 2 years ago
- ☆17Mar 1, 2026Updated 7 months ago
- Proton VPN Special Offer - Get 70% off • AdSpecial partner offer. Trusted by over 100 million users worldwide. Tested, Approved and Recommended by Experts.
- Error correction of long reads☆16Jan 30, 2026Updated 8 months ago
- Toolkit for calling structural variants using short or long reads☆119Aug 21, 2026Updated last month
- Tools for the analysis of structural variation in genomes☆81Feb 23, 2026Updated 7 months ago
- GeneMiner: a tool for extracting phylogenetic markers from next-generation sequencing data☆11Feb 22, 2024Updated 2 years ago
- Call regions of homozygosity and make tentative UPD calls☆12Jun 27, 2025Updated last year
- Repository for RecallME-v.0.1 a variant calling pipelines benchmarker and optimizer☆13Dec 18, 2023Updated 2 years ago
- Calling deletions using deep convolutional neural☆26Feb 12, 2020Updated 6 years ago
- A tool for estimating repeat sizes☆219Jan 30, 2024Updated 2 years ago
- Determining tandem repeat lengths using raw nanopore signals.☆15Sep 11, 2023Updated 3 years ago
- Deploy on Railway without the complexity - Free Credits Offer • AdConnect your repo and Railway handles the rest with instant previews. Quickly provision container image services, databases, and storage volumes.
- These scripts reformat a VCF into a SQLite database, with R☆15Jul 15, 2021Updated 5 years ago
- ☆21Nov 1, 2019Updated 6 years ago
- TIDDIT - structural variant calling☆80Jul 20, 2026Updated 2 months ago
- Ultra-fast, high-performing structural variation (SV) detector☆25Apr 26, 2023Updated 3 years ago
- A deletion and duplication caller from NGS paired-end data.☆14Aug 22, 2025Updated last year
- Polygenic score calculation from VCF in Nim.☆15Nov 22, 2020Updated 5 years ago
- ☆15Aug 22, 2023Updated 3 years ago
- A program to generate a graph which presents a simplified representation of several full length genomes☆13Aug 23, 2018Updated 8 years ago
- Detects human contamination in bam files☆16Sep 10, 2020Updated 6 years ago
- Deploy on Railway without the complexity - Free Credits Offer • AdConnect your repo and Railway handles the rest with instant previews. Quickly provision container image services, databases, and storage volumes.
- Structural variant merging tool☆58Aug 23, 2024Updated 2 years ago
- MetaSV: An accurate and integrative structural-variant caller for next generation sequencing☆59Jun 30, 2017Updated 9 years ago
- A deep learning approach to de novo variant calling in next generation sequencing data☆21Jun 19, 2026Updated 3 months ago
- ☆20Nov 17, 2025Updated 11 months ago
- Alignment-free genotyper for SNPs and short indels, implemented in Python.☆58Mar 7, 2025Updated last year
- Linear-time de novo Long Read Assembler☆43Mar 19, 2026Updated 6 months ago
- Accompanying analysis code for the FRASER manuscript☆25Aug 27, 2020Updated 6 years ago
- Detection and genotyping of structural variants☆23May 27, 2026Updated 4 months ago
- Sample Contamination Estimate from VCF☆21Nov 6, 2024Updated last year
- Deploy open-source AI quickly and easily - Special Bonus Offer • AdRunpod Hub is built for open source. One-click deployment and autoscaling endpoints without provisioning your own infrastructure.
- A minimap2 implementation with binseq inputs☆18Dec 11, 2025Updated 10 months ago
- FLT3 ITD detection (ITDseek) and simulation (ITDsim)☆14Feb 27, 2019Updated 7 years ago
- Structural variant benchmark☆25Mar 4, 2025Updated last year
- Basic UPD caller☆13Aug 23, 2021Updated 5 years ago
- Annotation and Ranking of Structural Variation☆310Aug 11, 2026Updated 2 months ago
- vcfdist: Accurately benchmarking phased variant calls☆90Aug 28, 2026Updated last month
- Pan-genome Construction and Population Structure Variation Calling pipeline☆46Sep 13, 2024Updated 2 years ago