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366 public repositories
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DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Updated
Oct 17, 2022
Python
Sampler, Sequencer, Multi-engine synth and effects - in a box! [WIP]
An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)
Official code repository for GATK versions 4 and up
Data intensive science for everyone.
Updated
Dec 1, 2022
Python
Analysis of single cell RNA-seq data course
fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing
Simple & Efficient data access for Scala and Scala.js
Updated
Nov 30, 2022
Scala
A Python library for creating and manipulating musical patterns, designed for use in algorithmic composition, generative music and sonification. Can be used to generate MIDI events, MIDI files, OSC messages, or custom events.
Updated
Nov 23, 2022
Python
A repository for setting up a RNAseq workflow
[MOVED] Moved to paoloshasta/shasta. De novo assembly from Oxford Nanopore reads
A Java API for high-throughput sequencing data (HTS) formats.
Updated
Nov 29, 2022
Java
Rapid large-scale prokaryote pan genome analysis
Updated
Apr 21, 2022
Perl
Intuitive graphical web interface for running BLAST bioinformatics tool (i.e. have your own custom NCBI BLAST site!)
Updated
Nov 19, 2022
JavaScript
Analysis Pipeline for Single Cell ATAC-seq
MiXCR is a universal software for fast and accurate extraction and downstream analysis of T- and B- cell receptor repertoires from any type of sequencing data. Free for academic use only.
A minimal and human-readable language and environment for the live coding of algorithmic electronic music.
Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data
Updated
May 14, 2020
Python
Python library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`
Updated
Nov 21, 2022
Python
Finds SNP sites from a multi-FASTA alignment file
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