Efficient pythonic random access to fasta subsequences
:scissors: :zap: Rapid haploid variant calling and core genome alignment
A React web application to query and share any PostgreSQL database.
Summarize, Analyze and Visualize MAF files from TCGA or in-house studies.
Oxford Nanopore's Basecaller
Performant Pythonic GenomicRanges
Haplotype VCF comparison tools
Implementation of Enformer, Deepmind's attention network for predicting ...
A One-Click System for Analyzing Loop-Resolution Hi-C Experiments
Sequence-to-graph mapper and graph generator
An open source platform for managing and analyzing biomedical big data
cython + htslib == fast VCF and BCF processing
annotate a VCF with other VCFs/BEDs/tabixed files
Personalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs
Fast, flexible and extensible genome browser.