Stars
A repository for collecting GPU basecalling stats
An R package and Colab notebook for variant effect calibration to ACMG/AMP evidence strength
Workflow to annotate SNVs, indels, and structural variants
for visual evaluation of read support for structural variation
MMseqs2: ultra fast and sensitive search and clustering suite
eLaRodON: identification of large genomic rearrangements in Oxford Nanopore sequencing data
Decoding biological age from face photographs using deep learning.
Combine structural variation outputs from long sequencing reads into a superior call set
A local-haplotagging-based small and structural variant caller
Data and analysis for NA12878 genome on nanopore
MiMo: Unlocking the Reasoning Potential of Language Model – From Pretraining to Posttraining
Variant calling tool for long-read sequencing data
MAS-Iso-Seq Isoform Identification and Quantification
ERVmap is one part curated database of human proviral ERV loci and one part a stringent algorithm to determine which ERVs are transcribed in their RNA seq data.
Whole Genome IVT for Nanopore DRS sequencing Control
sunnypilot is an open source driver assistance system. sunnypilot offers the user a unique driving experience for over 300 supported car makes and models with modified behaviors of driving assist e…
Hifiasm: a haplotype-resolved assembler for accurate Hifi reads
Source for the HL7 Genomics work group's "Clinical Genomics-Reporting" FHIR implementation guide
Read-Based Phasing Algorithm with Integrated Multi-Method Support for Enhanced Accuracy