waldronlab / HGNChelperView external linksLinks
Identify and correct invalid gene symbols
☆62Nov 16, 2024Updated last year
Alternatives and similar repositories for HGNChelper
Users that are interested in HGNChelper are comparing it to the libraries listed below
Sorting:
- amplicon/smMIP mapping and analysis pipeline☆11Dec 8, 2022Updated 3 years ago
- Tools for generating and decoding error-correcting DNA barcodes☆15Feb 15, 2022Updated 3 years ago
- The python binding for D4 format☆16Oct 22, 2021Updated 4 years ago
- Analysis pipeline for cancer sequencing data☆112Apr 30, 2025Updated 9 months ago
- High-intensity sequencing reveals the sources of plasma circulating cell-free DNA variants☆22Mar 27, 2020Updated 5 years ago
- Explore the cancer relevance of your gene list☆52Dec 17, 2025Updated last month
- Targeted and non-targeted anticancer drugs and drug regimens☆30Jan 21, 2026Updated 3 weeks ago
- ☆11Sep 5, 2018Updated 7 years ago
- Code and results from TotalSeqC antibody titration and pipeline benchmarking for CITE-seq experiments☆10Mar 13, 2021Updated 4 years ago
- Assembly and Annotation of the Human Immune Health Atlas☆20Aug 28, 2025Updated 5 months ago
- Filter and prioritize fusion calls☆20Jan 23, 2026Updated 3 weeks ago
- Quality control on genetic variants from next-generation sequencing data using random forest☆20May 26, 2022Updated 3 years ago
- ☆20Nov 30, 2023Updated 2 years ago
- Visualising single-cell trajectories, including comparisons between two models 📈☆32Dec 9, 2021Updated 4 years ago
- Reducing reference bias using multiple population reference genomes☆34May 27, 2024Updated last year
- R package containing useful functions for mutational signature analysis☆86Updated this week
- Example of run CytoSig and reproduce prediction results on bulk and single-cell cohorts☆14Jul 5, 2023Updated 2 years ago
- A tool to detect postzygotic single-nucleotide mosaicism from unpaired, trio, or paired samples.☆13Feb 23, 2021Updated 4 years ago
- This repository contains the source code of the revised version of MutPanning. MutPanning is publicly available under the BSD3-Clause ope…☆13Nov 12, 2019Updated 6 years ago
- An Artificial Neural Network-based discriminator for validating clinically significant genomic variants☆35Dec 25, 2023Updated 2 years ago
- VariantStore: A Large-Scale Genomic Variant Search Index☆39Jul 9, 2021Updated 4 years ago
- Bioconductor package for management of multi-assay data☆73Nov 17, 2025Updated 2 months ago
- Visualisation and prioritisation of genomic variants from human exome sequencing projects☆13Apr 23, 2019Updated 6 years ago
- ☆16Aug 8, 2025Updated 6 months ago
- Source code for the GWAS Diversity Monitor☆16Sep 1, 2025Updated 5 months ago
- ☆15Mar 15, 2023Updated 2 years ago
- MEM mapper prototype☆13Nov 28, 2020Updated 5 years ago
- ☆12Nov 19, 2023Updated 2 years ago
- UVC, a very accurate small-variant caller (https://doi.org/10.1093/bib/bbab458)☆14May 18, 2025Updated 8 months ago
- Single-pass probabilistic duplicate marking of alignments with a Bloom filter.☆22Aug 7, 2023Updated 2 years ago
- R package designed to simplify structural variant analysis☆74Dec 22, 2021Updated 4 years ago
- Repository for RecallME-v.0.1 a variant calling pipelines benchmarker and optimizer☆13Dec 18, 2023Updated 2 years ago
- dv-trio provides a pipeline to call variants for a trio (father-mother-child) using DeepVariants [1]. Genomic Variant Calling Files (gVCF…☆11Feb 3, 2021Updated 5 years ago
- functions and algorithms for single cell RNA-seq analyses☆12Jan 26, 2021Updated 5 years ago
- Multi-sample genome coverage viewer to observe large, coverage-based anomalies alongside annotations and sample metadata☆58Feb 17, 2022Updated 3 years ago
- We present a customizable computational tool, PathSeq2.0, to enable the discovery and identification of microbial sequences in metagenomi…☆12Jan 20, 2018Updated 8 years ago
- snakemake-based workflows☆12Jul 20, 2022Updated 3 years ago
- ☆344Apr 16, 2025Updated 9 months ago
- Fast Wilcoxon and auROC☆204Nov 8, 2024Updated last year