See how pathogenic your mutations are according to AlphaMissense based on your 23andme raw data
MIT License
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To be a next-generation DL-based phenotype prediction from genome mutations.
Consensus sequences for each Pango lineage
Automated Multi-Locus Sequence Analysis phylogenetic tree construction software
A collection of Python modules equivalent to R ReQTL Toolkit aims to identify the association bet...
Miscellaneous tools for genomics
REVertant MUTation Find & Verify
BS-Seeker3: An Ultra-fast, Versatile Pipeline for Mapping Bisulfite-treated Reads.
Reliable, scalable, efficient demultiplexing for single-cell RNA sequencing
Framework for integrated analysis and plotting of ChIP/RIP/RNA/*-seq data
HPC pipeline for overlapping V4 16S rRNA reads generated on Illumina MiSeq
Add biological annotations to variants in a given VCF file.
SARS-CoV-2 analysis pipeline for short-read, paired-end illumina sequencing
genes and genomes at your fingertips
Super sensitive mutation validator, uses sam/bam and vcf