A new tool to infer sex from massively parallel sequencing data.
☆17May 16, 2025Updated 11 months ago
Alternatives and similar repositories for seGMM
Users that are interested in seGMM are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- ThermoFisher Ion Torrent plugin to detect fetal trisomies and estimate fetal fraction☆17Mar 23, 2018Updated 8 years ago
- A tool kit to manage many variant on desktop computer☆13Jan 13, 2026Updated 3 months ago
- Variant Interpretation Pipeline☆49Apr 21, 2026Updated 2 weeks ago
- ☆27Mar 2, 2026Updated 2 months ago
- NiPTUNE. A Python library for NIPT analyses.☆11Nov 22, 2021Updated 4 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.
- Sample Contamination Estimate from VCF☆20Nov 6, 2024Updated last year
- do some exercise☆14Dec 2, 2025Updated 5 months ago
- ☆14Dec 13, 2023Updated 2 years ago
- Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data☆75Sep 4, 2024Updated last year
- PREFACE -- PREdict FetAl ComponEnt☆15Jan 2, 2026Updated 4 months ago
- These scripts reformat a VCF into a SQLite database, with R☆15Jul 15, 2021Updated 4 years ago
- CLI to automate Nextflow pipeline testing☆12Dec 15, 2025Updated 4 months ago
- Analysis pipelines for QTL discovery and GWAS signals interpretation☆12Sep 3, 2024Updated last year
- A Mendelian approach to variant effect prediction built in keras☆20Nov 3, 2025Updated 6 months ago
- GPUs on demand by Runpod - Special Offer Available • AdRun AI, ML, and HPC workloads on powerful cloud GPUs—without limits or wasted spend. Deploy GPUs in under a minute and pay by the second.
- WISECONDOR (WIthin-SamplE COpy Number aberration DetectOR): Detect fetal trisomies and smaller CNV's in a maternal plasma sample using wh…☆46Apr 24, 2024Updated 2 years ago
- a C++ API of htslib to be easily integrated and safely used. More importantly, it can be callled seamlessly in R/Python/Julia etc.☆24Aug 6, 2025Updated 8 months ago
- Coronavirus (SARS-Cov-2) sequencing analysis☆10Oct 5, 2021Updated 4 years ago
- ☆12Oct 11, 2024Updated last year
- ☆10Mar 4, 2025Updated last year
- Determine the biological sex of a human whole-genome BAM file☆16Feb 10, 2019Updated 7 years ago
- RTG Core: Software for alignment and analysis of next-gen sequencing data.☆49May 27, 2025Updated 11 months ago
- ☆16Oct 17, 2024Updated last year
- ☆15Apr 20, 2021Updated 5 years 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.
- Run multiple programs to check if a VCF is usable☆11May 15, 2020Updated 5 years ago
- Kraken2 Server☆23Nov 24, 2025Updated 5 months ago
- A collection of tools useful for preparing or manipulating site-frequency spectrum (SFS) files☆21Mar 20, 2023Updated 3 years ago
- A method for measuring chromosome-specific telomere length from long reads☆22May 20, 2024Updated last year
- Basic UPD caller☆12Aug 23, 2021Updated 4 years ago
- Pipeline to find aberrant events in RNA-Seq data, useful for diagnosis of rare disorders☆165Mar 24, 2026Updated last month
- Short-read and long-read sequencing tools for diagnostics☆176Updated this week
- SMN1 copy-number and sequence variant analysis from next generation sequencing data☆23Feb 20, 2026Updated 2 months ago
- Epigenetic cell-type deconvolution from Single-Cell Omic Reference profiles☆34Apr 4, 2025Updated last year
- 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.
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆41Apr 9, 2026Updated 3 weeks ago
- Prioritizing Copy Number Variants (CNV) using Phenotype and Gene Functional Similarity☆18Mar 10, 2022Updated 4 years ago
- ☆13Dec 3, 2018Updated 7 years ago
- Workshop: Using R/tidyverse to analyze & visualize gapminder/processed transcriptomics data!☆13Sep 12, 2025Updated 7 months ago
- ☆11May 21, 2024Updated last year
- ☆15Oct 3, 2017Updated 8 years ago
- Padlock design pipeline for multiplexed assay with multiple probes per target in cDNA-based expression profiling☆15Jul 11, 2024Updated last year