jnoms's Stars
zedr/clean-code-python
:bathtub: Clean Code concepts adapted for Python
nextflow-io/nextflow
A DSL for data-driven computational pipelines
dvanoni/notero
A Zotero plugin for syncing items and notes into Notion
bbuchfink/diamond
Accelerated BLAST compatible local sequence aligner.
ablab/spades
SPAdes Genome Assembler
Edinburgh-Genome-Foundry/DnaFeaturesViewer
:eye: Python library to plot DNA sequence features (e.g. from Genbank files)
philres/ngmlr
NGMLR is a long-read mapper designed to align PacBio or Oxford Nanopore (standard and ultra-long) to a reference genome with a focus on reads that span structural variations
cmdcolin/oddgenes
A small database of weird gene annotations
google-research/proteinfer
Deep networks for protein functional inference
refresh-bio/FAMSA
Algorithm for ultra-scale multiple sequence alignments (3M protein sequences in 5 minutes and 24 GB of RAM)
pirovc/genome_updater
Bash script to download/update snapshots of files from NCBI genomes repository (refseq/genbank) with track of changes and without redundancy
urmi-21/orfipy
Fast and flexible ORF finder
comprna/RATTLE
Reference-free reconstruction and error correction of transcriptomes from Nanopore long-read sequencing
hoelzer/poseidon
PoSeiDon: positive selection detection and recombination analysis pipeline
rega-cev/virulign
VIRULIGN: fast codon-correct alignment and annotation of viral genomes
jnoms/virID
Viral Identification and Discovery - A viral characterization pipeline built in Nextflow.
jnoms/SAT
Structural Analysis Toolkit - A python package for manipulation of structural data and structural alignments.
jnoms/virORF_direct
virORF_direct: Protein-level analysis of direct RNA sequencing data
jnoms/virKMER
viral KMER enrichment - Used to enrich viral reads in an input dataset
jnoms/ESCC_microbiome
Analysis and plotting scripts for the manuscript "An international report on bacterial communities in esophageal squamous cell carcinoma"
jnoms/SV40_transcriptome
Toolkit and pipeline for processing short- and long-read RNA sequencing data.