hanh1985's Stars
junegunn/vim-plug
:hibiscus: Minimalist Vim Plugin Manager
Xfennec/progress
Linux tool to show progress for cp, mv, dd, ... (formerly known as cv)
amaas/stanford_dl_ex
Programming exercises for the Stanford Unsupervised Feature Learning and Deep Learning Tutorial
ckreibich/scholar.py
A parser for Google Scholar, written in Python
lh3/bwa
Burrow-Wheeler Aligner for short-read alignment (see minimap2 for long-read alignment)
rstudio/tensorflow
TensorFlow for R
metachris/pdfx
Extract text, metadata and references (pdf, url, doi, arxiv) from PDF. Optionally download all referenced PDFs.
ContinuumIO/docker-images
Repository of Docker images created by Anaconda
pachterlab/kallisto
Near-optimal RNA-Seq quantification
marcelm/cutadapt
Cutadapt removes adapter sequences from sequencing reads
CrossRef/pdfextract
MOVED TO https://gitlab.com/crossref/pdfextract
seqan/seqan
SeqAn's official repository.
deweylab/RSEM
RSEM: accurate quantification of gene and isoform expression from RNA-Seq data
nanopore-wgs-consortium/NA12878
Data and analysis for NA12878 genome on nanopore
lukasz-wronski/vscode-ftp-sync
Ftp Sync plugin for Visual Studio Code
genome/bam-readcount
Count bases in BAM/CRAM files
OpenGene/awesome-bio-datasets
awesome-bio-datasets
AstraZeneca-NGS/VarDict
VarDict
knmnyn/ParsCit
An open-source CRF Reference String Parsing Package
OpenGene/MutScan
Detect and visualize target mutations by scanning FastQ files directly
datarootsio/artyfarty
ggplot2 theme + palette presets
paultpearson/TDAmapper
(R package) Analyze High-Dimensional Data Using Discrete Morse Theory
mateidavid/nanocall
An Oxford Nanopore Basecaller
OpenGene/OpenGene.jl
(No maintenance) OpenGene, core libraries for NGS data analysis and bioinformatics in Julia
OpenGene/CfdnaPattern
Pattern Recognition for Cell-free DNA
sfu-compbio/sinvict
SiNVICT: Ultra-Sensitive Detection of Single Nucleotide Variants and Indels in Circulating Tumour DNA
PeterUlz/Nucleosome_ctDNA
Inferring expressed genes by whole-genome sequencing of plasma DNA
WGLab/icages
iCAGES (integrated CAncer GEnome Score) is an effective tool for prioritizing cancer driver genes for a patient
Sage-Bionetworks-Challenges/SMC-RNA-Challenge
NimbleGen/bioinformatics
Bioinformatics tools developed at Roche NimbleGen