biopython by biopython

Official git repository for Biopython (originally converted from CVS)

created at March 15, 2009, 9:09 p.m.

Python

170 +0

4,169 +9

1,712 +1

GitHub
deepvariant by google

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

created at Nov. 23, 2017, 1:56 a.m.

Python

160 +0

3,077 +1

695 +1

GitHub
csvkit by wireservice

A suite of utilities for converting to and working with CSV, the king of tabular file formats.

created at April 1, 2011, 3 a.m.

Python

130 -1

5,817 +5

601 +1

GitHub
bcbio-nextgen by bcbio

Validated, scalable, community developed variant calling, RNA-seq and small RNA analysis

created at Feb. 6, 2013, 11:14 a.m.

Python

87 +0

973 -1

357 +0

GitHub
ChIP-seq-analysis by crazyhottommy

ChIP-seq analysis notes from Ming Tang

created at June 12, 2015, 9:42 p.m.

Python

65 +0

708 +6

290 +2

GitHub
RNA-seq-analysis by crazyhottommy

RNAseq analysis notes from Ming Tang

created at Aug. 26, 2015, 7:37 p.m.

Python

78 +0

839 +4

290 +0

GitHub
hail by hail-is

Cloud-native genomic dataframes and batch computing

created at Oct. 27, 2015, 8:55 p.m.

Python

55 +0

934 -2

235 +1

GitHub
PyVCF by jamescasbon

A Variant Call Format reader for Python.

created at Oct. 30, 2011, 4:52 p.m.

Python

31 +0

392 +0

199 +0

GitHub
pybedtools by daler

Python wrapper -- and more -- for BEDTools (bioinformatics tools for "genome arithmetic")

created at May 14, 2010, 9:09 p.m.

Python

17 +0

293 +0

103 +0

GitHub
bamsurgeon by adamewing

tools for adding mutations to existing .bam files, used for testing mutation callers

created at May 10, 2012, 10:18 p.m.

Python

15 +0

226 +1

83 +0

GitHub
gffutils by daler

GFF and GTF file manipulation and interconversion

created at Oct. 12, 2011, 1:48 p.m.

Python

14 +0

267 +2

74 +0

GitHub
pyfaidx by mdshw5

Efficient pythonic random access to fasta subsequences

created at Sept. 12, 2013, 7:02 p.m.

Python

9 +0

440 +0

73 +0

GitHub
pyensembl by openvax

Python interface to access reference genome features (such as genes, transcripts, and exons) from Ensembl

created at April 14, 2014, 3:23 p.m.

Python

22 +0

352 +0

66 +0

GitHub
bioservices by cokelaer

Access to Biological Web Services from Python.

created at Aug. 28, 2014, 3:24 p.m.

Python

18 +0

271 +0

61 +0

GitHub
AfterQC by OpenGene

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

created at Aug. 4, 2015, 2:08 p.m.

Python

20 +0

201 +0

51 +0

GitHub
bakta by oschwengers

Rapid & standardized annotation of bacterial genomes, MAGs & plasmids

created at Jan. 15, 2020, 11:08 p.m.

Python

14 +0

391 +5

42 +0

GitHub
cruzdb by brentp

python access to UCSC genomes database

created at Sept. 2, 2011, 3:36 p.m.

Python

17 +0

134 +1

41 +0

GitHub
redun by insitro

Yet another redundant workflow engine

created at Nov. 4, 2021, 12:14 a.m.

Python

15 +0

486 +2

37 +0

GitHub
ruffus by cgat-developers

CGAT-ruffus is a lightweight python module for running computational pipelines

created at Jan. 6, 2013, 10:20 p.m.

Python

11 +0

171 +0

34 +0

GitHub
seqmagick by fhcrc

An imagemagick-like frontend to Biopython SeqIO

created at Nov. 24, 2010, 12:48 a.m.

Python

12 +0

108 +0

22 +0

GitHub