A Rare Variant Caller for Array-based Genotyping
☆25Feb 25, 2015Updated 11 years ago
Alternatives and similar repositories for zCall
Users that are interested in zCall are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- ☆13Feb 10, 2021Updated 5 years ago
- Script to convert GTC/BPM files to VCF☆48Oct 13, 2025Updated 5 months ago
- Program for estimating admixture proportions and doing principal component analysis of a single NGS sample☆11Aug 15, 2024Updated last year
- R package for visualizing complex and multi-track 1D and 2D genomic data in GenomicRanges framework☆17Jan 7, 2025Updated last year
- processing illumina SNP arrays☆19Feb 3, 2017Updated 9 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.
- Evoker is a graphical tool for plotting genotype intensity data in order to assess quality of genotype calls. It implements a compact, bi…☆13Dec 21, 2017Updated 8 years ago
- Theano-based Deep Learning library (convnets, recurrent neural networks, and more).☆14Aug 2, 2017Updated 8 years ago
- Variant to disease dataset workflows for Open Targets Genetics☆13Aug 23, 2022Updated 3 years ago
- PrincetonPy's one-day workshop : Introduction to Python for Scientific Computing☆11Nov 4, 2015Updated 10 years ago
- A small repo for storing the code for making the files and html for CCRs.☆22Oct 22, 2019Updated 6 years ago
- A high-throughput analysis framework for Y-chromosomal next-generation sequencing data☆16Jun 11, 2021Updated 4 years ago
- 💻🔀🗑️ Randomly declutter your computer!☆10Oct 3, 2023Updated 2 years ago
- CNV calling algorithm for detection of homozygous and hemizygous deletions from whole exome sequencing data☆12Nov 9, 2025Updated 5 months ago
- Tools to convert Illumina IDAT/BPM/EGT/GTC and Affymetrix CEL/CHP files to VCF☆162Feb 26, 2026Updated last month
- 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.
- An R package for import, QC and analysis of Illumina Infinium genotyping arrays☆35Mar 20, 2018Updated 8 years ago
- Geneyx Analysis API☆12Apr 2, 2026Updated last week
- ☆31Jul 10, 2025Updated 9 months ago
- Graph-based alignment (Hierarchical Graph FM index)☆17Jul 23, 2019Updated 6 years ago
- Copy number vaiation detection from SNP arrays☆96May 19, 2024Updated last year
- DEPRECATED: Store and query public TCGA data☆11Sep 15, 2016Updated 9 years ago
- [Archived] SnakeMake pipeline to run BlobTools on public assemblies☆11Jul 3, 2023Updated 2 years ago
- Composite of Multiple Signals: tests for selection in meiotically recombinant populations☆14Jul 4, 2020Updated 5 years ago
- Learn and validate subtypes from multiple traits☆20Jun 15, 2021Updated 4 years ago
- Managed Database hosting by DigitalOcean • AdPostgreSQL, MySQL, MongoDB, Kafka, Valkey, and OpenSearch available. Automatically scale up storage and focus on building your apps.
- Rare variant test software for next generation sequencing data☆141Jan 26, 2022Updated 4 years ago
- GPA: Genetic analysis incorporating Pleiotropy and Annotation☆16Feb 27, 2020Updated 6 years ago
- Programming exercises to inspire kids to learn to program in a Minecraft type environment☆14Mar 24, 2019Updated 7 years ago
- ☆10Jan 20, 2023Updated 3 years ago
- ☆11Sep 18, 2017Updated 8 years ago
- Python package for cancer early detection based on a model of cancer evolution and circulating tumor DNA (ctDNA) shedding☆13Jan 8, 2021Updated 5 years ago
- Parse Copy Number Variation from Array and Sequencing☆18Dec 1, 2023Updated 2 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
- ChIP-seq DC and QC Pipeline☆36Mar 19, 2021Updated 5 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.
- ☆11Aug 21, 2018Updated 7 years ago
- Software program for generating synthetic datasets for genotypes and phenotypes☆18Jun 1, 2023Updated 2 years ago
- Pipeline to generate variant catalogues, a list of variants and their frequencies in a population, from whole genome sequences.☆13Jun 3, 2025Updated 10 months ago
- Automatic classification of sequence variants and CNVs according to ACMG criteria.☆28Sep 30, 2024Updated last year
- Annotate genomics variations of hg19 by using a BED format database, which construct from NCBI annotation release 104☆19Aug 4, 2023Updated 2 years ago
- Python library to parse file formats related to Illumina bead arrays☆48Jan 30, 2025Updated last year
- 一个中文基因数据库 面向专业人员也面向普通大众☆15Sep 20, 2018Updated 7 years ago