tools for adding mutations to existing .bam files, used for testing mutation callers
☆249Oct 18, 2024Updated last year
Alternatives and similar repositories for bamsurgeon
Users that are interested in bamsurgeon are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- RTG Tools: Utilities for accurate VCF comparison and manipulation☆335May 27, 2025Updated 11 months ago
- VarDict☆203Jan 5, 2024Updated 2 years ago
- Microassembly based somatic variant caller for NGS data☆154Jun 23, 2022Updated 3 years ago
- Somatic Variant Call for ctDNA☆12Mar 1, 2016Updated 10 years ago
- Haplotype VCF comparison tools☆467Dec 7, 2023Updated 2 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.
- GRIDSS: the Genomic Rearrangement IDentification Software Suite☆283May 21, 2025Updated last year
- Strelka2 germline and somatic small variant caller☆394Apr 20, 2026Updated last month
- A tool set for short variant discovery in genetic sequence data.☆205May 4, 2021Updated 5 years ago
- An ensemble approach to accurately detect somatic mutations using SomaticSeq☆205Apr 25, 2026Updated last month
- NEAT read simulation tools☆101Jun 22, 2022Updated 3 years ago
- VarDict Java port☆141Jan 5, 2024Updated 2 years ago
- A flexible framework for rapid genome analysis and interpretation☆319Oct 18, 2022Updated 3 years ago
- Detects human contamination in bam files☆16Sep 10, 2020Updated 5 years ago
- Generates synthetic cancer genomes with different contamination level and intra-tumor heterogeneity and devoid of any synthetic element☆11Sep 21, 2020Updated 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.
- Fast fusion detection using kallisto☆80Jun 11, 2025Updated 11 months ago
- Tools for working with SAM/BAM data☆610Dec 22, 2024Updated last year
- annotate a VCF with other VCFs/BEDs/tabixed files☆404May 1, 2026Updated 3 weeks ago
- a lightweight db framework for exploring genetic variation.☆328Apr 28, 2020Updated 6 years ago
- Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets☆38Jul 30, 2020Updated 5 years ago
- filtering trio-based genetic variants in VCFs for clinical review☆21Aug 18, 2020Updated 5 years ago
- Structural variant toolkit for VCFs☆411Updated this week
- Canvas - Copy number variant (CNV) calling from DNA sequencing data☆129Apr 20, 2026Updated last month
- This repository contains data indexes from NIST's Genome in a Bottle project.☆266Nov 30, 2023Updated 2 years ago
- Proton VPN Special Offer - Get 70% off • AdSpecial partner offer. Trusted by over 100 million users worldwide. Tested, Approved and Recommended by Experts.
- LoFreq Star: Sensitive variant calling from sequencing data☆113Oct 16, 2025Updated 7 months ago
- This repo provides tools to convert ClinVar data into a tab-delimited flat file, and also provides that resulting tab-delimited flat file…☆131Feb 13, 2020Updated 6 years ago
- Tools for working with genomic and high throughput sequencing data.☆366Updated this week
- fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing☆851May 2, 2026Updated 3 weeks ago
- Analysis pipeline for cancer sequencing data☆112Apr 24, 2026Updated last month
- Assembly Based ReAligner☆75May 24, 2018Updated 8 years ago
- Simultaneous detection of SNPs and Indels using a 16-genotype probabilistic model☆27Dec 26, 2023Updated 2 years ago
- TransVar - multiway annotator for precision medicine☆129Apr 19, 2023Updated 3 years ago
- Bayesian haplotype-based mutation calling☆323Feb 13, 2026Updated 3 months 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.
- ABRA2☆97Dec 2, 2022Updated 3 years ago
- ☆37Mar 16, 2021Updated 5 years ago
- Platypus Variant Caller☆107Jun 27, 2024Updated last year
- Estimate damage in standard NGS library preparation. Incompatible with library preparation methods from which the imbalance is lost (such…☆54Jun 5, 2017Updated 8 years ago
- iCAGES (integrated CAncer GEnome Score) is an effective tool for prioritizing cancer driver genes for a patient☆14Aug 18, 2022Updated 3 years ago
- robust matching of small variant datasets using flexible scoring schemes☆12Mar 26, 2020Updated 6 years ago
- Repository for the GA4GH Benchmarking Team work developing standardized benchmarking methods for germline small variant calls☆212Mar 19, 2021Updated 5 years ago