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:
- Bayesian-based fetal genotyping using maternal cell-free DNA and parental sequencing data.☆14Jun 5, 2019Updated 7 years ago
- R Package for Non Invasive Prenatal Testing (NIPT) analysis☆46Nov 5, 2019Updated 6 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
- Short reads aligner for NIPT/CNV☆16Oct 10, 2018Updated 8 years ago
- NiPTUNE. A Python library for NIPT analyses.☆11Nov 22, 2021Updated 4 years 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.
- CNV screening and annotation tool☆25Oct 31, 2016Updated 10 years ago
- ClassifyCNV: a tool for clinical annotation of copy-number variants☆76Jun 26, 2023Updated 3 years ago
- A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data☆13Updated this week
- Example client programs for Saphetor's VarSome annotation API☆36Oct 26, 2026Updated last week
- Linkage disequlibrium-informed PGT-A (LD-PGTA). A package for detecting genotypic signatures of aneuploidy from extremely low-coverage se…☆19Oct 10, 2022Updated 4 years ago
- Fast C code for identifying and removing primers and adapters☆11May 20, 2023Updated 3 years ago
- A Sliding Window Approach to Identify Differentially Methylated Regions Based on Whole Genome Bisulfite Sequencing☆14May 22, 2023Updated 3 years ago
- 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 5 months ago
- An RNA-Seq data exploration tool that shows read map coverage of a gene of interest along with a coloured "electronic fluorescent pictog…☆13Oct 16, 2026Updated 2 weeks ago
- Deploy to Railway using AI coding agents - Free Credits Offer • AdUse Claude Code, Codex, OpenCode, and more. Autonomous software development now has the infrastructure to match with Railway.
- A fast, robust and accurate variant calling software for human germline DNA analysis☆15Jun 30, 2026Updated 4 months ago
- Browser-based tool for visualizing and analyzing germline copy number variants in genomic data☆12Nov 7, 2024Updated last year
- ☆13Updated this week
- A toolkit to design standard primers, multiplexed primers, and primers around SV's☆13Oct 29, 2022Updated 4 years ago
- Pipeline for processing and analyzing CiFi data☆13Sep 24, 2026Updated last month
- ☆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
- ☆12Aug 20, 2025Updated last year
- ☆11Apr 25, 2024Updated 2 years ago
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting for WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Deploy in minutes on Cloudways by DigitalOcean.
- PREFACE -- PREdict FetAl ComponEnt☆16Oct 27, 2026Updated last week
- WisecondorX — An evolved WISECONDOR☆118Oct 20, 2026Updated 2 weeks ago
- A command-line interface for Sentieon pipelines☆17Updated this week
- K-RET: Knowledgeable Biomedical Relation Extraction System☆11Feb 22, 2025Updated last year
- Modelling and Analysis of Real-Time PCR Data☆11Aug 9, 2024Updated 2 years ago
- ☆129Sep 5, 2023Updated 3 years ago
- A project to develop the R Shiny applications.☆12May 13, 2019Updated 7 years ago
- A tool for sample swap identification in high throughput sequencing studies☆10Mar 4, 2025Updated last year
- 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.
- 🌓 Allele specific analyses across cell states and conditions☆11Nov 28, 2022Updated 3 years ago
- TNER: Tri-Nucleotide Error Reducer for ctDNA detection☆21Aug 23, 2019Updated 7 years ago
- A collection of utilities for working with next generation (MPS) sequencing data in Groovy☆15Sep 25, 2026Updated last month
- Functions for handling RNA-seq files and formats as input and output for scrattch functions.☆11Aug 20, 2025Updated last year
- 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
- Gene expression viewer template☆12Aug 30, 2017Updated 9 years ago
- ☆12Aug 17, 2024Updated 2 years ago