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GUI/CommandLine Tool Box for biologistists to utilize NGS data.
Long read based human genomic structural variation detection with cuteSV
SQANTI2 is now replaced by SQANTI3. Please go to: https://github.com/ConesaLab/SQANTI3
Fast and accurate de novo assembler for long reads
A markdown version emoji cheat sheet
an easy to use implementation of the NCBI taxonomy database for daily use
Ultrafast de novo assembly for long noisy reads (though having no consensus step)
Tensors and Dynamic neural networks in Python with strong GPU acceleration
A memory-efficient implementation of DenseNets
hemberg-lab / scRNA.seq.course
Forked from rstudio/bookdown-demoAnalysis of single cell RNA-seq data course
An Open Source Machine Learning Framework for Everyone
AiLearning:数据分析+机器学习实战+线性代数+PyTorch+NLTK+TF2
An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)
Scrapy, a fast high-level web crawling & scraping framework for Python.
ATLAS - Three commands to start analyzing your metagenome data
Official code repository for GATK versions 4 and up
KOBAS: a command line tool for identifying significant pathways from genomic data
Transcript assembly and quantification for RNA-Seq
classify, merge, tracking and annotation of GFF files by comparing to a reference annotation GFF
A content-first, sliding sidebar theme for Jekyll.
Genome-scale protein function classification
Scallop is a reference-based transcriptome assembler for RNA-seq
Next generation sequencing reads de novo assembler.