Pandaman-Ryan / AgentBindLinks
☆14Updated last year
Alternatives and similar repositories for AgentBind
Users that are interested in AgentBind are comparing it to the libraries listed below
Sorting:
- Code for paper "Principled feature attribution for unsupervised gene expression analysis"☆12Updated 2 years ago
- BPNet manuscript code.☆12Updated 4 years ago
- Comprehensive and scalable differential splicing analyses☆17Updated 2 weeks ago
- Flexible and efficient tests for evidence of positive selection anywhere in the cancer genome.☆26Updated 3 years ago
- Code for reproducing the Sei manuscript results☆17Updated 3 years ago
- Smooth-quantile Normalization Adaptation for Inference of co-expression Links☆16Updated 2 years ago
- ☆22Updated 2 months ago
- ☆18Updated last year
- A p-value-free method for controlling false discovery rates in high-throughput biological data with two conditions☆40Updated 3 years ago
- IRIS: Isoform peptides from RNA splicing for Immunotherapy target Screening☆27Updated last year
- Predicting TF sequence-specificity similarity with weighted alignments☆13Updated 6 years ago
- ☆12Updated 5 years ago
- rnalib: a python-based transcriptomics library☆11Updated last week
- LncADeep is an ab initio lncRNA identification and functional annotation tool based on deep learning☆28Updated 7 years ago
- ☆19Updated last year
- Perturb-seq analysis package☆16Updated last year
- Pipeline to call neoantigens from intron retention events derived from RNA-Seq data.☆28Updated 4 years ago
- ORF Quantification pipeline for Alternative Splicing☆16Updated 4 years ago
- Scatterbar - data visualization for proportional data across many spatially resolved coordinates☆11Updated 8 months ago
- ☆18Updated last year
- Chromatin interaction aware gene regulatory modeling with graph attention networks☆27Updated 2 years ago
- An R package to implement Differential Gene Set Enrichment Analysis (DGSEA): A statistical approach to quantify the relative enrichment o…☆14Updated 2 years ago
- NeoFuse is a user-friendly pipeline for the prediction of fusion neoantigens from tumor RNA-seq data.☆19Updated 3 years ago
- A Nextflow pipeline to align, merge, and organize large PhIP-Seq datasets☆13Updated 9 months ago
- DNA and RNA variant calling pipelines with HLA typing and Neoantigen predictions☆11Updated 4 years ago
- Source code for iDeLUCS. An interactive deep-learning based tool for clustering of genomic sequences☆15Updated last year
- epigenome analysis to rank transcription factors☆14Updated 5 years ago
- single-cell analysis workflows for double phosphoramidite barcode and UMI Correction (scCOLOR-seq)☆13Updated 2 years ago
- Modeling the genomic regulatory codes of fly, mouse, worm, and fish with deep learning☆17Updated 4 years ago
- Benchmarking long-read RNA-seq analysis tools☆27Updated 9 months ago