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Search results for fastq
fastq
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493 search results found
Oneliners
⭐
1,705
Useful bash one-liners for bioinformatics.
Fastp
⭐
1,602
An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging.
Seqtk
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1,148
Toolkit for processing sequences in FASTA/Q formats
Seqkit
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1,133
A cross-platform and ultrafast toolkit for FASTA/Q file manipulation
Fastq
⭐
790
Fast, in memory work queue
Bwa Mem2
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645
The next version of bwa-mem
Vsearch
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605
Versatile open-source tool for microbiome analysis
Wtdbg2
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401
Redbean: A fuzzy Bruijn graph approach to long noisy reads assembly
Trimgalore
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382
A wrapper around Cutadapt and FastQC to consistently apply adapter and quality trimming to FastQ files, with extra functionality for RRBS data
Seqan3
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373
The modern C++ library for sequence analysis. Contains version 3 of the library and API docs.
Juicer
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313
A One-Click System for Analyzing Loop-Resolution Hi-C Experiments
Bactopia
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281
A flexible pipeline for complete analysis of bacterial genomes
Bioinformatics One Liners
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277
Bioinformatics one liners from Ming Tang
Basecalling Comparison
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273
A comparison of different Oxford Nanopore basecallers
Krakentools
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242
KrakenTools provides individual scripts to analyze Kraken/Kraken2/Bracken/KrakenUniq output files
Zumis
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232
zUMIs: A fast and flexible pipeline to process RNA sequencing data with UMIs
Parallel Fastq Dump
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224
parallel fastq-dump wrapper
Pyfastx
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211
a python package for fast random access to sequences from plain and gzipped FASTA/Q files
Fastq Dl
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174
Download FASTQ files from SRA or ENA repositories.
Sickle
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166
Windowed Adaptive Trimming for fastq files using quality
Afterqc
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157
Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data
Rasusa
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156
Randomly subsample sequencing reads to a specified coverage
Gtz
⭐
156
A high performance and compression ratio compressor for genomic data, powered by GTXLab of Genetalks.
Genomics
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154
A collection of scripts and notes related to genomics and bioinformatics
Rust Bio Tools
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154
A set of command line utilities based on Rust-Bio.
Fastqe
⭐
152
FASTQ sequence quality visualisation with Emoji
Genozip
⭐
144
A modern compressor for genomic files (FASTQ, SAM/BAM/CRAM, VCF, FASTA, GFF/GTF/GVF, 23andMe...), up to 5x better than gzip and faster too
Rmats Turbo
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144
Nanopack
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143
Easily install all nanopack scripts together
Ngless
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141
NGLess: NGS with less work
Seed
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139
Efficient clustering of next generation sequences
Biofast
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132
Benchmarking programming languages/implementations for common tasks in Bioinformatics
Seq2science
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132
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.
Viral Ngs
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129
Viral genomics analysis pipelines
Mutscan
⭐
127
Detect and visualize target mutations by scanning FastQ files directly
Ngs Bits
⭐
121
Short-read sequencing tools
Qiita
⭐
118
Qiita - A multi-omics databasing effort
Fastq Pair
⭐
115
Match up paired end fastq files quickly and efficiently.
Repaq
⭐
110
A fast lossless FASTQ compressor with ultra-high compression ratio
Fastqt
⭐
109
FastQC port to Qt5: A quality control tool for high throughput sequence data.
Fastx_toolkit
⭐
109
FASTA/FASTQ pre-processing programs
Ngscheckmate
⭐
106
Software program for checking sample matching for NGS data
Readfq
⭐
105
Fast multi-line FASTA/Q reader in several programming languages
Fqtools
⭐
105
An efficient FASTQ manipulation suite
Isoquant
⭐
98
Transcript discovery and quantification with long RNA reads (Nanopores and PacBio)
Seqfu2
⭐
96
🚀 seqfu - Sequece Fastx Utilities
Fastqp
⭐
94
Simple FASTQ quality assessment using Python
Fetchngs
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93
Pipeline to fetch metadata and raw FastQ files from public and private databases
Assembly Stats
⭐
92
Get assembly statistics from FASTA and FASTQ files
Pandaseq
⭐
91
PAired-eND Assembler for DNA sequences
Beetl
⭐
90
BEETL
Cljam
⭐
87
A DNA Sequence Alignment/Map (SAM) library for Clojure
Adapterremoval
⭐
87
AdapterRemoval v2 - rapid adapter trimming, identification, and read merging
Pipeline Structural Variation
⭐
87
Pipeline for calling structural variations in whole genomes sequencing Oxford Nanopore data
Fastq Tools
⭐
86
Small utilities for working with fastq sequence files.
Genefuse
⭐
86
Gene fusion detection and visualization
Soapnuke
⭐
85
A Tool for integrated Quality Control and Preprocessing on FASTQ or BAM/CRAM files
Mcclintock
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83
Meta-pipeline to identify transposable element insertions using next generation sequencing data
Illumina Utils
⭐
82
A library and collection of scripts to work with Illumina paired-end data (for CASAVA 1.7+ pipeline).
Nullarbor
⭐
80
💾 📃 "Reads to report" for public health and clinical microbiology
Ngsutils
⭐
80
Tools for next-generation sequencing analysis
Idba
⭐
80
Ratatosk
⭐
76
Hybrid error correction of long reads using colored de Bruijn graphs
Fqgrep
⭐
75
Grep for FASTQ files
Celescope
⭐
73
Single Cell Analysis Pipelines
Neat Genreads
⭐
72
NEAT read simulation tools
Phylosift
⭐
68
Phylogenetic and taxonomic analysis for genomes and metagenomes
Qcat
⭐
64
qcat is a Python command-line tool for demultiplexing Oxford Nanopore reads from FASTQ files.
Scatac Pro
⭐
64
A comprehensive tool for processing, analyzing and visulizing single cell chromatin accessibility sequencing data
Nanostat
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63
Create statistic summary of an Oxford Nanopore read dataset
Opengene.jl
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61
(No maintenance) OpenGene, core libraries for NGS data analysis and bioinformatics in Julia
Seq_io
⭐
60
FASTA and FASTQ parsing in Rust
Cobs
⭐
58
COBS - Compact Bit-Sliced Signature Index (for Genomic k-Mer Data or q-Grams)
Fastqcr
⭐
57
fastqcr: Quality Control of Sequencing Data
Fasten
⭐
57
👷 Fasten toolkit, for streaming operations on fastq files
Fastv
⭐
56
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.
Pyflow Chipseq
⭐
55
a snakemake pipeline to process ChIP-seq files from GEO or in-house
Fq
⭐
54
Command line utility for manipulating Illumina-generated FASTQ files.
Dnaio
⭐
52
Efficiently read and write sequencing data from Python
Rattle
⭐
51
Reference-free reconstruction and error correction of transcriptomes from Nanopore long-read sequencing
Dna Nn
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51
Model and predict short DNA sequence features with neural networks
Poreplex
⭐
51
A versatile sequenced read processor for nanopore direct RNA sequencing
Falco
⭐
50
A C++ drop-in replacement of FastQC to assess the quality of sequence read data
Fastq And Furious
⭐
49
Efficient handling of FASTQ files from Python
Metacache
⭐
49
memory efficient, fast & precise taxnomomic classification system for metagenomic read mapping
Fastx.jl
⭐
48
Parse and process FASTA and FASTQ formatted files of biological sequences.
Gto
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47
A genomics-proteomics toolkit
Raptor
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46
A fast and space-efficient pre-filter for querying very large collections of nucleotide sequences.
Bamtofastq
⭐
45
Convert 10x BAM files to the original FASTQs compatible with 10x pipelines
Fastaq
⭐
45
Python3 scripts to manipulate FASTA and FASTQ files
Umicollapse
⭐
44
Accelerating the deduplication and collapsing process for reads with Unique Molecular Identifiers (UMI). Heavily optimized for scalability and orders of magnitude faster than a previous tool.
Bam Tricks
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44
Tip and tricks for BAM files
W2rap Contigger
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44
An Illumina PE genome contig assembler, can handle large (17Gbp) complex (hexaploid) genomes.
Pauvre
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43
Pauvre: QC and genome browser plotting Oxford Nanopore and PacBio long reads.
Cfdnapattern
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42
Pattern Recognition for Cell-free DNA
Fastq Screen
⭐
42
Detecting contamination in NGS data and multi-species analysis
Bio
⭐
42
Bioinformatic infrastructure libraries
Ngspeciesid
⭐
41
Reference-free clustering and consensus forming of long-read amplicon sequencing
Pbsim2
⭐
40
PBSIM2: a simulator for long read sequencers with a novel generative model of quality scores
Mutmap
⭐
40
MutMap pipeline to identify causative mutations responsible for a phenotype
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Perl Fastq (101)
C Fastq (99)
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