smoe

SOLIDWORKS-Linux-Wine-Version-

This is a project, where I give you a way to use SOLIDWORKS on Linux!

abc

ABC: System for Sequential Logic Synthesis and Formal Verification

Augustus

Genome annotation with AUGUSTUS

bioperl-live

Core BioPerl 1.x code

boinc

Open-source software for volunteer computing and grid computing.

bx-python

Tools for manipulating biological data, particularly multiple sequence alignments

catfishq

Cat FASTQ files

cuteSV

Long read based human genomic structural variation detection with cuteSV

DeepAb

Deep learning models and structure realization scripts for the DeepAb antibody structure prediction method.

DiscoSnp

DiscoSnp is designed for discovering all kinds of SNPs (not only isolated ones), as well as insertions and deletions, from raw set(s) of reads.

fastd

Fast and Secure Tunnelling Daemon

gatb-core

Core library of the Genome Analysis Toolbox with de-Bruijn graph

gffutils

GFF and GTF file manipulation and interconversion

Gridcoin-Research

Gridcoin-Research

kexpr-nim

nim wrapper for Heng Li's kexpr math expression evaluator library

lcnc-bullseye-installer

macintosh.js

🖥 A virtual Apple Macintosh with System 8, running in Electron. I'm sorry.

mCaller

A python program to call methylation (m6A in DNA) from nanopore signal data

mesaflash

Configuration and diagnostic tool for Mesa Electronics PCI(E)/ETH/EPP/USB/SPI boards

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

openwrt

This repository is a mirror of https://git.openwrt.org/openwrt/openwrt.git It is for reference only and is not active for check-ins or for reporting issues. We will continue to accept Pull Requests here. They will be merged via staging trees then into openwrt.git. All issues should be reported at: https://bugs.openwrt.org

picard

A set of command line tools (in Java) for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF.

pigx_rnaseq

Pipeline for RNAseq

pokrok

Use any progress bar package with a simple API (production)

rigraph

igraph R package

seqtk

Toolkit for processing sequences in FASTA/Q formats

SSUsearch

A pipeline for extracting SSU rRNA gene from wgs data and applying them for further diversity analysis

STAR

RNA-seq aligner

tandem-genotypes

VirSorter2

customizable pipeline to identify viral sequences from (meta)genomic data