一个中文基因数据库 面向专业人员也面向普通大众
☆15Sep 20, 2018Updated 8 years ago
Alternatives and similar repositories for genedb
Users that are interested in genedb are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Haplotype-based somatic genome simulator☆10Apr 20, 2026Updated 6 months ago
- ☆15May 22, 2025Updated last year
- Recording personal workflows used in work, study notes, and summaries of various tools and methods.☆11Oct 9, 2025Updated last year
- Notebooks to illustrate how BigFISH is working.☆12Sep 5, 2022Updated 4 years ago
- Analyze exome data for Mendelian disorders. Still in alpha-testing.☆10Apr 13, 2016Updated 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.
- A small repo for storing the code for making the files and html for CCRs.☆22Oct 22, 2019Updated 7 years ago
- Detects human contamination in bam files☆16Sep 10, 2020Updated 6 years ago
- Deconvolving tumor purity and ploidy by integrating copy number alterations and loss of heterozygosity☆40Jul 19, 2017Updated 9 years ago
- eXtasy: Variant Prioritization by Genomic Data Fusion☆13Feb 19, 2014Updated 12 years ago
- ☆11Sep 18, 2017Updated 9 years ago
- ancestry☆11Nov 14, 2017Updated 8 years ago
- DEPRECATED: Store and query public TCGA data☆11Sep 15, 2016Updated 10 years ago
- Visualize next generation sequencing reads over putative structural variants☆13Aug 25, 2014Updated 12 years ago
- cfDNA Sequencing Pipeline with UMI☆12Jun 11, 2026Updated 4 months 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.
- Advanced plotting functions for CNV data generated by CNV-Seq and Control Freec☆13Aug 25, 2020Updated 6 years ago
- Integrated Variant Caller☆17Mar 15, 2018Updated 8 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
- iCAGES (integrated CAncer GEnome Score) is an effective tool for prioritizing cancer driver genes for a patient☆14Aug 18, 2022Updated 4 years ago
- ☆16Jun 21, 2023Updated 3 years ago
- iAnnotateSV is a Python library and command-line software toolkit to annotate and visualize structural variants detected from Next Genera…☆16Jun 11, 2026Updated 4 months ago
- This project contains simple methods to measure sample relatedness and identify potential swaps and contamination☆10Jan 8, 2016Updated 10 years ago
- DL model to predict HLA peptide presentation☆17Jan 31, 2024Updated 2 years ago
- IBD based kinship estimation☆16Mar 3, 2023Updated 3 years ago
- Proton VPN Special Offer - Get 70% off • AdSpecial partner offer. Trusted by over 100 million users worldwide. Tested, Approved and Recommended by Experts.
- VVP (VAAST Variant Prioritizer) rapidly prioritizes genetic variants☆18Mar 10, 2018Updated 8 years ago
- Genetic visualization application using Python/Flask, Angular, d3, and 23andMe authentication☆14Aug 5, 2016Updated 10 years ago
- Single-pass probabilistic duplicate marking of alignments with a Bloom filter.☆22Aug 7, 2023Updated 3 years ago
- ☆14Dec 13, 2023Updated 2 years ago
- shifts hg19/38 genomic position for feasible input format.☆12Jun 8, 2023Updated 3 years ago
- ☆11Sep 11, 2024Updated 2 years ago
- ☆21Feb 24, 2023Updated 3 years ago
- Data visualization code generation benchmark: Evaluates LLMs' ability to generate visualization code from DataFrame descriptions.☆13Nov 28, 2025Updated 11 months ago
- ☆10Jun 9, 2020Updated 6 years 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.
- ⛏ HLA predictions from NGS shotgun data☆58Sep 3, 2026Updated 2 months ago
- Core Hunter 3: a flexible core subset selection tool☆10Sep 11, 2025Updated last year
- Multiplex Primer Design☆21Oct 30, 2020Updated 6 years ago
- This project consists of three parts: Random forest model for GC diagnosis and Predict the survival outcomes of GC patient using RSF meth…☆32Nov 15, 2024Updated last year
- This is a read-only mirror of the CRAN R package repository. sequenza — Copy Number Estimation from Tumor Genome Sequencing Data. Homep…☆22May 9, 2019Updated 7 years ago
- learning python by doing practices☆16Sep 26, 2017Updated 9 years ago
- Instructions and analysis scripts for single cell Higher Order Testing (scHOT)☆10Oct 7, 2020Updated 6 years ago