☆11Mar 16, 2020Updated 6 years ago
Alternatives and similar repositories for DL4VC
Users that are interested in DL4VC are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- ☆10Dec 8, 2022Updated 3 years ago
- Deep Learning based variant calling toolkit - https://clara-parabricks.github.io/VariantWorks/☆49Aug 20, 2025Updated last year
- This repository contains a list of tools or methods that have been used in GIAB analysis☆28Nov 15, 2019Updated 6 years ago
- Getting started guide to using GPUs for nCoV2019 research☆14Apr 24, 2020Updated 6 years ago
- Efficient base quality score recalibrator for NGS data☆24Nov 28, 2015Updated 10 years ago
- 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.
- Simple and efficient access to genomic data for deep learning models.☆43Jan 9, 2020Updated 6 years ago
- Removing PCR duplicates for sequencing reads.☆14Sep 8, 2020Updated 6 years ago
- DNN-based small variant caller☆12May 2, 2022Updated 4 years ago
- A model builder helper for creating graph neural networks akin to the ones described in https://arxiv.org/abs/1806.01261 and https://ie…☆12Apr 18, 2019Updated 7 years ago
- ☆10Dec 28, 2023Updated 2 years ago
- PyTorch Implementation of DeepSequence☆12Aug 13, 2019Updated 7 years ago
- Client side iobio library for building and executing iobio commands☆10Dec 31, 2018Updated 7 years ago
- Detect somatic variants from tumor and normal WGS/WXS data☆21Sep 21, 2026Updated last month
- ☆10Jul 15, 2023Updated 3 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.
- SANEFALCON (Single reAds Nucleosome-basEd FetAL fraCtiON): Calculating the fetal fraction for noninvasive prenatal testing based on genom…☆14Jun 5, 2020Updated 6 years ago
- Arioc: GPU-accelerated DNA short-read alignment☆70May 20, 2025Updated last year
- A simple calendar program in D, to demonstrate its component-programming features☆13Mar 11, 2022Updated 4 years ago
- React frontend to varapp☆10Sep 7, 2016Updated 10 years ago
- Course material for CSAMA 2015: Statistics and Computing in Genome Data Science☆11Mar 15, 2023Updated 3 years ago
- D Text User Interface library☆12Jun 28, 2019Updated 7 years ago
- ☆10Jun 5, 2018Updated 8 years ago
- ☆11Feb 26, 2015Updated 11 years ago
- A C++14 library for NGS data formats☆39Aug 5, 2019Updated 7 years ago
- 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.
- SDK for GPU accelerated genome assembly and analysis☆305May 3, 2024Updated 2 years ago
- A Flexible Generative Framework for Graph-based Semi-supervised Learning (NeurIPS 2019)☆16Nov 14, 2021Updated 4 years ago
- GenNotes – public consensus annotation of genetic variants☆11Mar 27, 2016Updated 10 years ago
- Aligner for sequencing data☆18Apr 20, 2026Updated 6 months ago
- Virtual Pharmacist is a web tool that interprets personal genome for the impact of genetic variation on drug response. It can take varian…☆13Nov 16, 2015Updated 10 years ago
- Ultrafast consensus module for raw de novo genome assembly of long uncorrected reads. http://genome.cshlp.org/content/early/2017/01/18/gr…☆303May 9, 2024Updated 2 years ago
- Provides an advanced search for browser bookmarks and histories.☆12May 17, 2025Updated last year
- Genevieve genome report tool☆14Dec 8, 2022Updated 3 years ago
- Light Cube using PYNQ☆10Aug 4, 2018Updated 8 years ago
- Managed Kubernetes at scale on DigitalOcean • AdDigitalOcean Kubernetes includes the control plane, bandwidth allowance, container registry, automatic updates, and more for free.
- EPIDEMIC is an easy-to-run Matlab/Octave educational toolkit for epidemiological analysis.☆18Apr 4, 2025Updated last year
- Software for comparing contact maps from HiC, CaptureC and other 3D genome data.☆26May 21, 2018Updated 8 years ago
- Report generator for Chanjo output☆10Jun 5, 2024Updated 2 years ago
- Call regions of homozygosity and make tentative UPD calls☆12Jun 27, 2025Updated last year
- WIP Jupyter notebook for the D programming language / DSLs written in D☆11Jun 10, 2019Updated 7 years ago
- This project contains a set of scripts to facilitate the setup of the Jetson Nano for doing Deep Learning with Tensorflow 2.0 (and also w…☆11Oct 25, 2019Updated 7 years ago
- ☆12Dec 8, 2021Updated 4 years ago