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
Alternatives and similar repositories for NIPT-FFMLP
Users that are interested in NIPT-FFMLP are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- R Package for Non Invasive Prenatal Testing (NIPT) analysis☆46Nov 5, 2019Updated 6 years ago
- Short reads aligner for NIPT/CNV☆16Oct 10, 2018Updated 7 years ago
- SANEFALCON (Single reAds Nucleosome-basEd FetAL fraCtiON): Calculating the fetal fraction for noninvasive prenatal testing based on genom…☆14Jun 5, 2020Updated 6 years ago
- Bayesian-based fetal genotyping using maternal cell-free DNA and parental sequencing data.☆14Jun 5, 2019Updated 7 years ago
- NiPTUNE. A Python library for NIPT analyses.☆11Nov 22, 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.
- Example client programs for Saphetor's VarSome annotation API☆37Aug 5, 2026Updated last week
- A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data☆13Aug 4, 2026Updated last week
- A GPU-friendly implementation of SpliceAI☆11Dec 8, 2022Updated 3 years ago
- NIPT-human-genetics is a semi-automated workflow designed for the analysis of large-scale ultra-low-pass non-invasive prenatal test (NIPT…☆14May 30, 2026Updated 2 months ago
- Browser-based tool for visualizing and analyzing germline copy number variants in genomic data☆12Nov 7, 2024Updated last year
- A collection of utilities for working with next generation (MPS) sequencing data in Groovy☆15Aug 8, 2026Updated last week
- This is the official development repository for BaseVar, which call variants for large-scale ultra low-pass (<1.0x) WGS data, especially …☆28May 28, 2026Updated 2 months ago
- ☆10Mar 23, 2022Updated 4 years ago
- Automation Report is a product that can solve the needs related to report generation in many industries. The original intention of this p…☆32Jan 11, 2024Updated 2 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.
- A toolkit to design standard primers, multiplexed primers, and primers around SV's☆13Oct 29, 2022Updated 3 years ago
- PREFACE -- PREdict FetAl ComponEnt☆15Jan 2, 2026Updated 7 months ago
- A project to develop the R Shiny applications.☆12May 13, 2019Updated 7 years ago
- WisecondorX — An evolved WISECONDOR☆116Jul 1, 2026Updated last month
- A pipeline for the identification of Compound Heterozygous Variants☆10Nov 10, 2022Updated 3 years ago
- An RNA-Seq data exploration tool that shows read map coverage of a gene of interest along with a coloured "electronic fluorescent pictog…☆13Jun 18, 2026Updated last month
- Gene expression viewer template☆12Aug 30, 2017Updated 8 years ago
- This is a pipeline for variant annotation in the diagnosis of rare genetic disorders. It relies on open source data and has instructions …☆17Mar 20, 2023Updated 3 years ago
- Python Essentials for Biomedical Data Analysis: An Introductory Guide☆15Aug 14, 2025Updated last year
- Deploy on Railway without the complexity - Free Credits Offer • AdConnect your repo and Railway handles the rest with instant previews. Quickly provision container image services, databases, and storage volumes.
- A tool for sample swap identification in high throughput sequencing studies☆10Mar 4, 2025Updated last year
- 🌓 Allele specific analyses across cell states and conditions☆11Nov 28, 2022Updated 3 years ago
- BrainSeq Phase II project lead by LIBD for the BrainSeq Consortium☆11Jan 7, 2024Updated 2 years ago
- TNER: Tri-Nucleotide Error Reducer for ctDNA detection☆21Aug 23, 2019Updated 6 years ago
- Glue between Clinical Genomics apps☆12Updated this week
- Regulatory Element Locus Intersection (RELI) Analysis☆14Jun 12, 2026Updated 2 months ago
- 基于rstudio、code-server、jupyter-lab的dockerfile，用于快速搭建数据分析环境。☆57Nov 14, 2022Updated 3 years ago
- High-fidelity 5mC DNA methylation detection model for PacBio HiFi reads☆13Apr 10, 2026Updated 4 months ago
- Documentation for the ISB-CGC on Read the Docs.☆11Jul 15, 2026Updated last month
- 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.
- A simple script to create a customizable html file from an AnnotSV output.☆22Apr 20, 2026Updated 3 months ago
- ☆19Jun 2, 2026Updated 2 months ago
- Mutation tracker for microbial genomes☆14Sep 30, 2020Updated 5 years ago
- BAMixChecker: A fast and efficient tool for sample matching checkup☆16Jun 12, 2022Updated 4 years ago
- Advanced plotting functions for CNV data generated by CNV-Seq and Control Freec☆13Aug 25, 2020Updated 5 years ago
- Custom alterations based on Mkdocs-Material☆15Mar 16, 2025Updated last year
- ☆36Aug 7, 2025Updated last year