Here are
508 public repositories
matching this topic...
DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Updated
Jun 2, 2022
Python
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
Jun 3, 2022
Python
C library for high-throughput sequencing data formats
Tools to process and analyze deep sequencing data.
Updated
May 18, 2022
Python
Java utilities for Bioinformatics
A collection of awesome things regarding all omics.
Customizable workflows based on snakemake and python for the analysis of NGS data
Updated
Jun 2, 2022
Python
A One-Click System for Analyzing Loop-Resolution Hi-C Experiments
Updated
Apr 29, 2022
Shell
A collection of Galaxy-related training material
A Java API for high-throughput sequencing data (HTS) formats.
Tools for working with genomic and high throughput sequencing data.
Updated
Jun 2, 2022
Scala
R package for analyzing single-cell RNA-seq data
UGENE is free open-source cross-platform bioinformatics software
Bioconvert is a collaborative project to facilitate the interconversion of life science data from one format to another.
Updated
Apr 15, 2022
Python
Detect and visualize target mutations by scanning FastQ files directly
Software pipeline for the analysis of CRISPR-Cas9 genome editing outcomes from sequencing data
Updated
May 17, 2019
Python
Sequana: a set of Snakemake NGS pipelines
Updated
May 25, 2022
Jupyter Notebook
An NGS read trimming tool that is specific, sensitive, and speedy. (production)
Updated
Jul 29, 2021
Python
Cloud agnostic genomics analysis, scientific computation and storage platform
Rare variant test software for next generation sequencing data
Accurate and flexible loops calling tool for 3D genomic data.
Updated
May 19, 2022
Python
Automated and customizable preprocessing of Next-Generation Sequencing data, including full (sc)ATAC-seq, ChIP-seq, and (sc)RNA-seq workflows. Works equally easy with public as local data.
Updated
Jun 2, 2022
Python
TPMCalculator quantifies mRNA abundance directly from the alignments by parsing BAM files
Annotation and Ranking of Structural Variation
Generate duplex/single consensus reads to reduce sequencing noises and remove duplications
An ultra-fast tool for identification of SARS-CoV-2 and other microbes from sequencing data. This tool can be used to detect viral infectious diseases, like COVID-19.
GATK RNA-Seq Variant Calling in Nextflow
Updated
Aug 25, 2021
Nextflow
Improve this page
Add a description, image, and links to the
ngs
topic page so that developers can more easily learn about it.
Curate this topic
Add this topic to your repo
To associate your repository with the
ngs
topic, visit your repo's landing page and select "manage topics."
Learn more
You can’t perform that action at this time.
You signed in with another tab or window. Reload to refresh your session.
You signed out in another tab or window. Reload to refresh your session.
When working with very large SAM files it is often convenient to remove sequence and quality information to reduce storage and improve I/O.
Following from this it would be convenient to have a
stripSeqQualfunction that replaces the two fields with*.