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Wellcome Sanger Institute
- Cambridge, UK
- https://orcid.org/0000-0001-9110-7441
- @vitaliikl
Highlights
- Pro
Stars
A command-line tool to mitigate homology-based data leakage in sequence-to-expression models
Ledidi turns any machine learning model into a biological sequence editor, allowing you to design sequences with desired properties.
UCE is a zero-shot foundation model for single-cell gene expression data
vitkl / scvi-tools
Forked from scverse/scvi-toolsDeep generative models for single-cell omics data
Decima is a Python library to train sequence models on single-cell RNA-seq data.
Join subcellular Visium HD bins into cells
Pipeline for designing custom probes against human genes
A declarative interactive genomics visualization library for Python.
A count based method for detecting doublets from single nucleus ATAC-seq (snATAC-seq) data.
a scalable python suite for tree inference and advanced pseudotime analysis from scRNAseq data.
Gaussian process regression package for counts data with negative binomial and zero-inflated negative binomial likelihoods
Comprehensive mapping of tissue cell architecture via integrated single cell and spatial transcriptomics (cell2location model)
Scentinel is a probabilistic ensemble framework designed for mapping large single-cell (sc) multi-omic datasets using either transductive or inductive transfer learning. The framework operates on p…
cell2module: decomposing scRNA and scATAC cell identity into gene modules using count-based Bayesian NMF
vitkl / scENTInEL
Forked from haniffalab/scENTInELScentinel is a probabilistic ensemble framework designed for mapping large single-cell (sc) multi-omic datasets using either transductive or inductive transfer learning. The framework operates on p…
A method for analyzing scATAC-seq experiments.
sequence-based prediction of multiscale genome structure from kilobase to whole-chromosome scale