A tool for visualizing alignments of reads in regions containing tandem repeats
☆92Apr 20, 2026Updated 6 months 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☆219Jan 30, 2024Updated 2 years ago
- ☆23Sep 21, 2021Updated 5 years ago
- A suite of tools for detecting expansions of short tandem repeats☆86Jul 6, 2023Updated 3 years ago
- ☆36Apr 20, 2026Updated 6 months ago
- Detect novel (and reference) STR expansions from short-read data☆72Dec 6, 2025Updated 10 months ago
- Bare Metal GPUs on DigitalOcean Gradient AI • AdPurpose-built for serious AI teams training foundational models, running large-scale inference, and pushing the boundaries of what's possible.
- A tool that lets you quickly flip through images in a local directory and record notes or answer questions about each one.☆23Jul 23, 2026Updated 3 months ago
- A tool for diagnosing SMA in exome, genome or targeted sequencing data☆14Jul 1, 2026Updated 4 months ago
- Structural Variation breakpoint discovery via adaptive learning☆17Jul 6, 2023Updated 3 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
- Structural variant pipeline☆18Jun 25, 2020Updated 6 years ago
- Tandem repeat genotyping and visualization from PacBio HiFi data☆145Jun 10, 2026Updated 4 months ago
- A tool for profiling long STRs from short reads☆107Apr 19, 2021Updated 5 years ago
- Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat☆42Updated this week
- Toolkit for calling and analyzing de novo STR mutations☆17Dec 17, 2023Updated 2 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.
- Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data☆75Sep 4, 2024Updated 2 years ago
- Data and information about the Polaris study☆56Nov 18, 2019Updated 6 years ago
- a python extension of CNVnator -- a tool for CNV analysis from depth-of-coverage by mapped reads☆219Jun 23, 2026Updated 4 months ago
- Unfazed by genomic variant phasing☆29May 26, 2024Updated 2 years ago
- Genotype and phase short tandem repeats using Illumina whole-genome sequencing data☆108Feb 27, 2023Updated 3 years ago
- Detects human contamination in bam files☆16Sep 10, 2020Updated 6 years ago
- Scripts and utilities for analyzing tandem repeats (TRs).☆53Updated this week
- A copy number caller for SMN1 and SMN2 to enable SMA diagnosis and carrier screening with WGS☆51Oct 14, 2023Updated 3 years ago
- Structural Variant Index☆77Jul 1, 2026Updated 4 months 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.
- Plot structural variant signals from many BAMs and CRAMs☆573Jul 13, 2024Updated 2 years ago
- A tool for genotyping Variable Number Tandem Repeats (VNTR) from sequence data☆49Dec 6, 2024Updated last year
- don't get DUP'ed or DEL'ed by your putative SVs.☆109Dec 14, 2020Updated 5 years ago
- A machine learning tool to predict tandem repeat pathogenicity