A tool for visualizing alignments of reads in regions containing tandem repeats
☆90Dec 19, 2023Updated 2 years ago
Alternatives and similar repositories for REViewer
Users that are interested in REViewer are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- A tool for estimating repeat sizes☆207Jan 30, 2024Updated 2 years ago
- ☆23Sep 21, 2021Updated 4 years ago
- ☆35Nov 1, 2021Updated 4 years ago
- Scripts and utilities for analyzing tandem repeats (TRs).☆43Mar 19, 2026Updated last week
- A tool for diagnosing SMA in exome, genome or targeted sequencing data☆13Apr 30, 2025Updated 10 months ago
- End-to-end encrypted cloud storage - Proton Drive • AdSpecial offer: 40% Off Yearly / 80% Off First Month. Protect your most important files, photos, and documents from prying eyes.
- A suite of tools for detecting expansions of short tandem repeats☆85Jul 6, 2023Updated 2 years ago
- Detect novel (and reference) STR expansions from short-read data☆70Dec 6, 2025Updated 3 months ago
- A tool that lets you quickly flip through images in a local directory and record notes or answer questions about each one.☆21Jan 4, 2026Updated 2 months ago
- Data and information about the Polaris study☆56Nov 18, 2019Updated 6 years ago
- A machine learning tool to predict tandem repeat pathogenicity☆12Jan 2, 2024Updated 2 years ago
- Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat☆39Dec 15, 2025Updated 3 months ago
- Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data☆75Sep 4, 2024Updated last year
- Tandem repeat genotyping and visualization from PacBio HiFi data☆133Dec 8, 2025Updated 3 months ago
- A lightweight, alignment-free utility for detecting repeat-containing reads in short-read WGS, WES and RNA-seq data.☆18Jan 16, 2026Updated 2 months ago
- Virtual machines for every use case on DigitalOcean • AdGet dependable uptime with 99.99% SLA, simple security tools, and predictable monthly pricing with DigitalOcean's virtual machines, called Droplets.
- a python extension of CNVnator -- a tool for CNV analysis from depth-of-coverage by mapped reads☆212Mar 16, 2026Updated last week
- Automatised pipeline of ConsensuSV workflow.☆24Aug 23, 2023Updated 2 years ago
- Structural Variation breakpoint discovery via adaptive learning☆17Jul 6, 2023Updated 2 years ago
- TRGT Repeat expansion summary☆11Apr 10, 2023Updated 2 years ago
- Structural variant pipeline☆18Jun 25, 2020Updated 5 years ago
- ☆24Jul 29, 2025Updated 7 months ago
- Unfazed by genomic variant phasing☆27May 26, 2024Updated last year
- De novo tandem repeat calling from PacBio HiFi data☆19Dec 5, 2025Updated 3 months ago
- A phenotype-based tool for variant prioritization in WES and WGS data☆42Nov 21, 2022Updated 3 years ago
- 1-Click AI Models by DigitalOcean Gradient • AdDeploy popular AI models on DigitalOcean Gradient GPU virtual machines with just a single click and start building anything your business needs.
- A tool for genotyping Variable Number Tandem Repeats (VNTR) from sequence data☆47Dec 6, 2024Updated last year
- ☆19Mar 14, 2022Updated 4 years ago
- A CNN model to identify MEIs in WGS☆13Mar 4, 2025Updated last year
- Toolkit for genome-wide analysis of tandem repeats☆60Feb 19, 2026Updated last month
- a hidden Markov model to infer simple repeats from genome sequences☆37Feb 19, 2021Updated 5 years ago
- Toolkit for calling and analyzing de novo STR mutations☆17Dec 17, 2023Updated 2 years ago
- HAT is a set of tools for calling de novo variants from whole-genome sequencing data.☆24Nov 18, 2025Updated 4 months ago
- ☆21Aug 30, 2022Updated 3 years ago
- A tool to genotype CYP2D6 with WGS data☆55Oct 14, 2023Updated 2 years ago
- Simple, predictable pricing with DigitalOcean hosting • AdAlways know what you'll pay with monthly caps and flat pricing. Enterprise-grade infrastructure trusted by 600k+ customers.
- A python wrapper around SURVIVOR☆20Feb 15, 2024Updated 2 years ago
- Detects human contamination in bam files☆16Sep 10, 2020Updated 5 years ago
- Non-parametric structural variant genotyper☆15Nov 18, 2021Updated 4 years ago
- A tool for profiling long STRs from short reads☆105Apr 19, 2021Updated 4 years ago
- A copy number caller for SMN1 and SMN2 to enable SMA diagnosis and carrier screening with WGS☆51Oct 14, 2023Updated 2 years ago
- Evaluate variant calls and its combination with k-mer multiplicity☆67Dec 2, 2022Updated 3 years ago
- Structural Variant Index☆76Dec 13, 2024Updated last year