deepvariant by google

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

updated at May 23, 2024, 1:24 p.m.

Python

159 +0

3,097 +5

697 +1

GitHub
hifiasm by chhylp123

Hifiasm: a haplotype-resolved assembler for accurate Hifi reads

updated at May 23, 2024, 1:39 p.m.

C++

29 +0

486 +3

83 +1

GitHub
mosdepth by brentp

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

updated at May 23, 2024, 3:09 p.m.

Nim

23 +0

662 +2

99 +0

GitHub
freebayes by freebayes

Bayesian haplotype-based genetic polymorphism discovery and genotyping.

updated at May 23, 2024, 3:11 p.m.

C++

46 +0

751 +2

259 +0

GitHub
FastQC by s-andrews

A quality control analysis tool for high throughput sequencing data

updated at May 23, 2024, 4:03 p.m.

Java

13 +0

398 +2

80 +0

GitHub
MMseqs2 by soedinglab

MMseqs2: ultra fast and sensitive search and clustering suite

updated at May 23, 2024, 7:04 p.m.

C

31 +0

1,275 +4

181 +1

GitHub
vcftools by vcftools

A set of tools written in Perl and C++ for working with VCF files, such as those generated by the 1000 Genomes Project.

updated at May 24, 2024, 12:47 a.m.

C++

32 +0

482 +2

147 +0

GitHub
wgsim by lh3

Reads simulator

updated at May 24, 2024, 1:36 a.m.

C

17 +0

250 +1

89 +1

GitHub
zindex by mattgodbolt

Create an index on a compressed text file

updated at May 24, 2024, 3:50 a.m.

C

23 +0

612 +0

41 +0

GitHub
nextflow by nextflow-io

A DSL for data-driven computational pipelines

updated at May 24, 2024, 4:17 a.m.

Groovy

85 +0

2,567 +3

594 +0

GitHub
bowtie2 by BenLangmead

A fast and sensitive gapped read aligner

updated at May 24, 2024, 7:19 a.m.

C++

30 +0

627 +4

161 -1

GitHub
AfterQC by OpenGene

Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data

updated at May 24, 2024, 7:31 a.m.

Python

20 +0

203 +2

50 +0

GitHub
ngs-preprocess by fmalmeida

A pipeline for preprocessing NGS data from Illumina, Nanopore and PacBio technologies

updated at May 24, 2024, 8:04 a.m.

Nextflow

4 +0

30 +2

4 +0

GitHub
AGAT by NBISweden

Another Gtf/Gff Analysis Toolkit

updated at May 24, 2024, 8:17 a.m.

Perl

47 +1

419 +4

52 +0

GitHub
samtools by samtools

Tools (written in C using htslib) for manipulating next-generation sequencing data

updated at May 24, 2024, 9:30 a.m.

C

100 +0

1,562 +4

572 +0

GitHub
bwa by lh3

Burrow-Wheeler Aligner for short-read alignment (see minimap2 for long-read alignment)

updated at May 24, 2024, 10:30 a.m.

C

107 +0

1,458 +3

547 +0

GitHub
seqkit by shenwei356

A cross-platform and ultrafast toolkit for FASTA/Q file manipulation

updated at May 24, 2024, 12:05 p.m.

Go

27 +0

1,218 +3

156 +0

GitHub
Flye by fenderglass

De novo assembler for single molecule sequencing reads using repeat graphs

updated at May 24, 2024, 1:43 p.m.

C

28 +0

735 +4

160 +0

GitHub
genozip by divonlan

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

updated at May 24, 2024, 2 p.m.

C

1 +0

149 +0

11 +1

GitHub
bpipe by ssadedin

Bpipe - a tool for running and managing bioinformatics pipelines

updated at May 24, 2024, 2:14 p.m.

Groovy

18 -1

224 +1

57 +0

GitHub