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sequencing

DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.

Python
3514
24 天前

Sampler, Sequencer, Multi-engine synth and effects - in a box! [WIP]

C++
2672
3 年前

An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)

C++
2189
24 天前

Official code repository for GATK versions 4 and up

Java
1856
1 天前

SPAdes Genome Assembler

C++
870
20 天前

fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing

Nim
776
18 天前

Simple & Efficient data access for Scala and Scala.js

Scala
494
20 天前

A repository for setting up a RNAseq workflow

R
445
8 年前

A Python package 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 actions.

Python
404
1 个月前

MiXCR is an ultimate software platform for analysis of Next-Generation Sequencing (NGS) data for immune profiling.

Kotlin
376
12 天前

Rapid large-scale prokaryote pan genome analysis

Perl
354
3 年前

A minimal and human-readable language and environment for the live coding of algorithmic electronic music.

Max
345
17 小时前

Analysis Pipeline for Single Cell ATAC-seq

R
319
2 年前

A Java API for high-throughput sequencing data (HTS) formats.

Java
287
9 天前

Intuitive graphical web interface for running BLAST bioinformatics tool (i.e. have your own custom NCBI BLAST site!)

JavaScript
287
13 天前

Python library to parse, format, validate, normalize, and map sequence variants according to HGVS Nomenclature (https://hgvs-nomenclature.org/).

Python
283
1 个月前

SortMeRNA: next-generation sequence filtering and alignment tool

C++
277
2 个月前

[MOVED] Moved to paoloshasta/shasta. De novo assembly from Oxford Nanopore reads

C++
273
3 年前