chapmanb / bcbbLinks
Incubator for useful bioinformatics code, primarily in Python and R
☆645Updated last year
Alternatives and similar repositories for bcbb
Users that are interested in bcbb are comparing it to the libraries listed below
Sorting:
- Validated, scalable, community developed variant calling, RNA-seq and small RNA analysis☆1,026Updated last year
- Bioinformatics code libraries and scripts☆555Updated 6 months ago
- Python for Bioinformatics☆262Updated 5 years ago
- Tools to process and analyze deep sequencing data.☆751Updated 6 months ago
- Efficient pythonic random access to fasta subsequences☆482Updated 5 months ago
- Java utilities for Bioinformatics☆516Updated this week
- A list of useful bioinformatics resources☆623Updated 9 months ago
- python module to plot beautiful and highly customizable genome browser tracks☆862Updated last year
- A basic introduction to Biopython, intended for a classroom based workshop. Now on Codeberg.☆226Updated 5 years ago
- Bayesian haplotype-based genetic polymorphism discovery and genotyping.☆862Updated 8 months ago
- bedtools - the swiss army knife for genome arithmetic☆1,021Updated 10 months ago
- The Ensembl Variant Effect Predictor predicts the functional effects of genomic variants☆529Updated last week
- ☆320Updated 5 years ago
- Customizable workflows based on snakemake and python for the analysis of NGS data☆397Updated 2 weeks ago
- Tools for handling Unique Molecular Identifiers in NGS data sets☆535Updated 2 weeks ago
- A curated list of nextflow based pipelines☆620Updated 7 months ago
- Graph-based alignment (Hierarchical Graph FM index)☆525Updated last week
- DNA plotting library for Python☆301Updated last year
- Trinity RNA-Seq de novo transcriptome assembly☆881Updated last year
- RSEM: accurate quantification of gene and isoform expression from RNA-Seq data☆460Updated last year
- Pysam is a Python package for reading, manipulating, and writing genomics data such as SAM/BAM/CRAM and VCF/BCF files. It's a lightweight…☆877Updated last week
- Python wrapper -- and more -- for BEDTools (bioinformatics tools for "genome arithmetic")☆328Updated 10 months ago
- A tool to map bisulfite converted sequence reads and determine cytosine methylation states☆442Updated 6 months ago
- A wrapper around Cutadapt and FastQC to consistently apply adapter and quality trimming to FastQ files, with extra functionality for RRBS…☆537Updated 2 weeks ago
- Bioinformatics containers☆772Updated 3 months ago
- Fast genome-wide functional annotation through orthology assignment☆697Updated 7 months ago
- Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing☆541Updated this week
- Bioinformatics one liners from Ming Tang☆500Updated 5 years ago
- MACS -- Model-based Analysis of ChIP-Seq☆768Updated last week
- Aggregate results from bioinformatics analyses across many samples into a single report.☆1,417Updated 3 weeks ago