Chromosomes from karyotype images
☆13May 29, 2019Updated 7 years ago
Alternatives and similar repositories for Chromosome-Images
Users that are interested in Chromosome-Images are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Banding pattern extraction and banding pattern segmentation mask generation for stained banded chromosome images.☆20Jun 10, 2022Updated 4 years ago
- Machine Learning (ML) research within medicine and healthcare represents one of the most challenging domains for both engineers and medic…☆18Aug 1, 2020Updated 6 years ago
- Chromosome image segmentation using Keras☆14Feb 25, 2017Updated 9 years ago
- Source code and data set of the paper CIR-Net: Automatic Classification of Human Chromosome based on Inception-ResNet Architecture☆20Jan 5, 2021Updated 5 years ago
- ☆10Mar 23, 2022Updated 4 years ago
- AI Agents on DigitalOcean Gradient AI Platform • AdBuild production-ready AI agents using customizable tools or access multiple LLMs through a single endpoint. Create custom knowledge bases or connect external data.
- Separating Overlapping Chromosomes with SegNet.☆14Jun 18, 2020Updated 6 years ago
- Translocator: local realignment and global remapping enabling accurate translocation detection using single-molecule sequencing long read…☆12Jan 22, 2020Updated 6 years ago
- ☆48Apr 19, 2017Updated 9 years ago
- NiPTUNE. A Python library for NIPT analyses.☆11Nov 22, 2021Updated 4 years ago
- This repository provides cytogenetics related datasets to investigate the semantic segmentation☆35Oct 25, 2025Updated last year
- ☆13Apr 1, 2026Updated 7 months ago
- ☆12Nov 14, 2016Updated 9 years ago
- ☆13May 2, 2018Updated 8 years ago
- Short reads aligner for NIPT/CNV☆16Oct 10, 2018Updated 8 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.
- NIPT-human-genetics is a semi-automated workflow designed for the analysis of large-scale ultra-low-pass non-invasive prenatal test (NIPT…☆15May 30, 2026Updated 5 months ago
- ☆15Aug 22, 2023Updated 3 years ago
- A tool to analyze telomeric reads from WGS or telobait-capture long-read sequencing data☆10Oct 1, 2024Updated 2 years ago
- Glue between Clinical Genomics apps☆12Updated this week
- DNN-based small variant caller☆12May 2, 2022Updated 4 years ago
- ☆16Jan 10, 2022Updated 4 years ago
- Implementation of the ASN.1 BER rules for IEC 61850 GOOSE Messaging☆13Dec 17, 2018Updated 7 years ago
- 用每个窗口的read数作为特征、胎儿浓度作为标签，训练神经网络模型；训练完成的神经网络模型可用于NIPT胎儿浓度的预测☆11Jun 10, 2022Updated 4 years ago
- a library to generate and resolve packets defined in IEC 61850☆14May 13, 2016Updated 10 years ago
- 1-Click AI Models by DigitalOcean Gradient • AdDeploy popular AI models on DigitalOcean Gradient GPU virtual machines with just a single click. Zero configuration with optimized deployments.
- Browser-based tool for visualizing and analyzing germline copy number variants in genomic data☆12Nov 7, 2024Updated 2 years ago
- Passive network mapping tool written in Ruby☆15Apr 8, 2014Updated 12 years ago
- Phase reads, assemble haplotypes and detect SVs☆19Nov 11, 2020Updated 5 years ago
- nPoRe: n-Polymer Realigner for improved pileup-based variant calling☆19Jul 11, 2022Updated 4 years ago
- Modelling and Analysis of Real-Time PCR Data☆11Aug 9, 2024Updated 2 years ago
- Bayesian-based fetal genotyping using maternal cell-free DNA and parental sequencing data.☆14Jun 5, 2019Updated 7 years ago
- VCF files of SVs using long-read sequencing (LRS).☆22Dec 17, 2021Updated 4 years ago
- Python Essentials for Biomedical Data Analysis: An Introductory Guide☆15Aug 14, 2025Updated last year
- A collection of utilities for working with next generation (MPS) sequencing data in Groovy☆15Sep 25, 2026Updated last month
- Serverless GPU API endpoints on Runpod - Get Bonus Credits • AdSkip the infrastructure headaches. Auto-scaling, pay-as-you-go, no-ops approach lets you focus on innovating your application.
- Ultra-fast, high-performing structural variation (SV) detector☆25Apr 26, 2023Updated 3 years ago
- Population-scale detection of non-reference sequence variants using colored de Bruijn Graphs☆27Apr 29, 2024Updated 2 years ago
- Structural variant benchmark☆25Mar 4, 2025Updated last year
- RNA sequence design for a target protein sequence☆13Jun 2, 2026Updated 5 months ago
- Detect key Units in mosaic Tandem Repeats from representative reads from the same locus☆10Aug 2, 2023Updated 3 years ago
- ☆25Feb 1, 2014Updated 12 years ago
- Identifies duplicate reads. This tool locates and tags duplicate reads in a coordinate ordered SAM or BAM file.☆31Jan 21, 2026Updated 9 months ago