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
- A lightweight, alignment-free utility for detecting repeat-containing reads in short-read WGS, WES and RNA-seq data.☆19Jan 16, 2026Updated 9 months ago
- A Mendelian approach to variant effect prediction built in keras☆22Aug 22, 2026Updated 2 months ago
- Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat☆42Oct 28, 2026Updated 2 weeks 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.
- Error correction of long reads☆16Jan 30, 2026Updated 9 months ago
- Population-scale detection of non-reference sequence variants using colored de Bruijn Graphs☆27Apr 29, 2024Updated 2 years ago
- ☆23Sep 21, 2021Updated 5 years ago
- ☆18Mar 1, 2026Updated 8 months ago
- TIDDIT - structural variant calling☆81Jul 20, 2026Updated 3 months ago
- Toolkit for calling structural variants using short or long reads☆120Updated this week
- Tools for the analysis of structural variation in genomes☆81Feb 23, 2026Updated 8 months ago
- Call regions of homozygosity and make tentative UPD calls☆12Jun 27, 2025Updated last year
- GeneMiner: a tool for extracting phylogenetic markers from next-generation sequencing data☆11Feb 22, 2024Updated 2 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.
- Repository for RecallME-v.0.1 a variant calling pipelines benchmarker and optimizer☆13Dec 18, 2023Updated 2 years ago
- Detection and genotyping of structural variants☆24May 27, 2026Updated 5 months ago
- Calling deletions using deep convolutional neural☆26Feb 12, 2020Updated 6 years ago
- A tool for estimating repeat sizes☆220Jan 30, 2024Updated 2 years ago
- ☆21Nov 1, 2019Updated 7 years ago
- Determining tandem repeat lengths using raw nanopore signals.☆15Sep 11, 2023Updated 3 years ago
- nPoRe: n-Polymer Realigner for improved pileup-based variant calling☆19Jul 11, 2022Updated 4 years ago
- Polygenic score calculation from VCF in Nim.☆15Nov 22, 2020Updated 5 years ago
- ☆57Jan 11, 2023Updated 3 years ago
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting for WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Deploy in minutes on Cloudways by DigitalOcean.
- Ultra-fast, high-performing structural variation (SV) detector☆25Apr 26, 2023Updated 3 years ago
- Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data☆73Sep 4, 2024Updated 2 years ago
- Pipeline for structural variant image curation and analysis.☆49Dec 5, 2021Updated 4 years ago
- These scripts reformat a VCF into a SQLite database, with R☆15Jul 15, 2021Updated 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
- A tool to detect structural variant☆17Mar 27, 2023Updated 3 years ago
- Example datasets for CNVkit (http://github.com/etal/cnvkit)☆23Aug 18, 2018Updated 8 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.
- Panache is a web-based interface designed for the visualization of linearized pangenomes. It can be used to show presence/absence informa…☆51Jun 7, 2023Updated 3 years ago
- Sample Contamination Estimate from VCF☆21Oct 23, 2026Updated 3 weeks ago
- software for analysis of chromatin feature occupancy profiles from high-throughput sequencing data☆18Nov 26, 2019Updated 6 years ago
- ☆20Nov 17, 2025Updated 11 months ago
- ClassifyCNV: a tool for clinical annotation of copy-number variants☆76Jun 26, 2023Updated 3 years ago
- A deletion and duplication caller from NGS paired-end data.☆14Aug 22, 2025Updated last year
- A minimap2 implementation with binseq inputs☆18Dec 11, 2025Updated 11 months ago
Are these results useful?