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A framework for stock data fetching, persistence and analysing

Python 152 49 Updated May 21, 2023

Deconvolving tumor purity and ploidy by integrating copy number alterations and loss of heterozygosity

Python 40 15 Updated Jul 19, 2017

DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.

Python 3,634 772 Updated Oct 21, 2025

Roadmap of DL and ML, some courses, study notes and paper summary

758 191 Updated Oct 8, 2018

Data and code for generating proteomaps

HTML 4 3 Updated Jul 4, 2023

MaxQuant Automated Pipeline

Python 24 10 Updated Jun 13, 2020

pymzML - an interface between Python and mzML Mass spectrometry Files

Python 183 95 Updated Feb 3, 2026

LC-MS data processing tool for large-scale metabolomics experiments.

C++ 91 52 Updated Jul 11, 2022

🗂️ [vdjdb.com is up and running!] Git-based TCR database storage & management. Submissions welcome!

Python 152 27 Updated Feb 22, 2026

A repository for setting up a RNAseq workflow

R 454 181 Updated Apr 10, 2017

HGVS variant name parsing and generation

Python 176 78 Updated Jun 14, 2023

Create Bloom filters for a given reference and then use it to categorize sequences

C++ 76 16 Updated Nov 26, 2024

Kart: A divide-and-conquer algorithm for NGS read mapping with high error tolerance

C 26 6 Updated May 21, 2020

A versatile pairwise aligner for genomic and spliced nucleotide sequences

C 2,128 456 Updated Feb 13, 2026

De novo assembly based variant calling pipeline for Illumina short reads

TeX 110 21 Updated Nov 30, 2020

This repository holds the companion project to Goby3, used to train and evaluate deep learning models to call variations. This repository contains the Matcha framework to help train and evaluate de…

Java 51 20 Updated Jun 1, 2018

DeTiN is designed to measure tumor-in-normal contamination and improve somatic variant detection sensitivity when using a contaminated matched control.

Jupyter Notebook 53 22 Updated May 20, 2022

Analysis of Cancer Genomes; 2017 edition

HTML 16 16 Updated Jan 21, 2018

Calculates the Variant Allele Fraction of variants in VCF files

Perl 19 3 Updated Nov 28, 2024

Variant Calling in Cancer Genomes

HTML 8 4 Updated Mar 11, 2018

🙃 A delightful community-driven (with 2,400+ contributors) framework for managing your zsh configuration. Includes 300+ optional plugins (rails, git, macOS, hub, docker, homebrew, node, php, python…

Shell 184,988 26,294 Updated Feb 25, 2026

🐟 🍣 🍱 Highly-accurate & wicked fast transcript-level quantification from RNA-seq reads using selective alignment

C++ 862 183 Updated May 29, 2024

A comprehensive pipeline to analyze and visualize structural variants

Shell 20 3 Updated Jan 28, 2020

Technical experimentations to beat the stock market using deep learning 📈

Python 483 157 Updated Mar 4, 2017

An opinionated list of awesome Python frameworks, libraries, software and resources.

Python 284,710 27,248 Updated Feb 25, 2026

TensorFlow Tutorial and Examples for Beginners (support TF v1 & v2)

Jupyter Notebook 43,800 14,805 Updated Jul 26, 2024

A curated list of awesome deep learning applications in the field of computational biology

1,964 314 Updated Nov 7, 2021

Peptide-MHC I binding affinity prediction

Python 232 68 Updated Feb 17, 2026

Python3 wrapper for GATB-Core.

Python 10 3 Updated Dec 16, 2017

TADbit is a complete Python library to deal with all steps to analyze, model and explore 3C-based data. With TADbit the user can map FASTQ files to obtain raw interaction binned matrices (Hi-C like…

Python 108 63 Updated Nov 12, 2025
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