Official git repository for Biopython (originally converted from CVS)
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Official git repository for Biopython (originally converted from CVS)
RNA-seq aligner
Deep probabilistic analysis of single-cell and spatial omics data
🦖 ClawBio - The first bioinformatics-native AI agent skill library. Local-first. Reproducible. Open. Free.
Validated, scalable, community developed variant calling, RNA-seq and small RNA analysis
C library for high-throughput sequencing data formats
In-memory nucleotide sequence k-mer counting, filtering, graph traversal and more
DNABERT: pre-trained Bidirectional Encoder Representations from Transformers model for DNA-language in genome
Tasks Assessing Protein Embeddings (TAPE), a set of five biologically relevant semi-supervised learning tasks spread across different domains of protein biology.
A Go package for engineering organisms.
Generation of protein sequences and evolutionary alignments via discrete diffusion models
Fast, sensitive and accurate integration of single-cell data with Harmony
Lightweight, super fast C/C++ (& Python) library for sequence alignment using edit (Levenshtein) distance.
Spatial Single Cell Analysis in Python
R package for detecting doublets in single-cell RNA sequencing data
A tool for semi-automatic cell type classification
SCENIC is an R package to infer Gene Regulatory Networks and cell types from single-cell RNA-seq data.
Sequential regulatory activity predictions with deep convolutional neural networks.
Reference mapping for single-cell genomics
Native R and Python sample-deletion robustness for omics: candidate certificates, minimum deletion bounds, Bioconductor model refits and donor-level pseudobulk
RNA-seq prediction with deep convolutional neural networks.
Bi-Directional Equivariant Long-Range DNA Sequence Modeling
Haplotype-aware CNV analysis from single-cell RNA-seq, ATAC-seq, and multiome
Genomic sequence storage, indexing and alignment inside PostgreSQL: https://bioseqdb.com/