mergesam by DarwinAwardWinner

Automate common sam & bam conversions

updated at Jan. 6, 2016, 2:02 a.m.

Python

3 +0

6 +0

1 +0

GitHub
bam-toolbox by AndersenLab

A bam toolbox

updated at March 4, 2020, 12:06 a.m.

Python

10 +0

1 +0

1 +0

GitHub
ruffus by cgat-developers

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

updated at Dec. 15, 2023, 2:59 a.m.

Python

11 +0

171 +0

34 +0

GitHub
cyvcf by arq5x

A fast Python library for VCF files leveraging Cython for speed.

updated at Jan. 22, 2024, 10:32 a.m.

Python

6 +0

52 +0

13 +0

GitHub
easy_qsub by shenwei356

Easily submitting multiple PBS jobs or running local jobs in parallel. Multiple input files supported.

updated at March 13, 2024, 5:58 a.m.

Python

3 +0

28 +0

8 +0

GitHub
smof by incertae-sedis

Explore and analyze biological sequence data

updated at March 17, 2024, 5:55 p.m.

Python

3 +0

15 +0

2 +0

GitHub
fastqp by mdshw5

Simple FASTQ quality assessment using Python

updated at March 25, 2024, 9:06 a.m.

Python

6 +0

107 +0

14 +0

GitHub
squiggle by IQTLabs

📈 DNA Sequence Visualization for Humans

updated at March 27, 2024, 4:50 a.m.

Python

6 +0

38 +0

9 +0

GitHub
seqmagick by fhcrc

An imagemagick-like frontend to Biopython SeqIO

updated at March 31, 2024, 9:30 p.m.

Python

12 +0

108 +0

22 +0

GitHub
pybedtools by daler

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

updated at April 11, 2024, 12:51 a.m.

Python

17 +0

293 +0

104 +0

GitHub
ggd-cli by gogetdata

The command-line interface to GGD

updated at April 17, 2024, 12:59 p.m.

Python

5 +0

42 +0

3 +0

GitHub
cruzdb by brentp

python access to UCSC genomes database

updated at April 23, 2024, 8:01 p.m.

Python

17 +0

134 +0

42 +0

GitHub
poapy by ljdursi

A simple Partial Order Aligner based on Lee, Grasso and Sharlow (2002), for education/demonstration purposes

updated at April 29, 2024, 5:18 p.m.

Python

8 +0

69 +0

12 +0

GitHub
wormtable by wormtable

Write-once-read-many table for large datasets.

updated at May 1, 2024, 10:03 p.m.

Python

6 +0

28 +0

5 +0

GitHub
PyVCF by jamescasbon

A Variant Call Format reader for Python.

updated at May 9, 2024, 10:25 a.m.

Python

31 +0

393 +0

200 +1

GitHub
pyfaidx by mdshw5

Efficient pythonic random access to fasta subsequences

updated at May 13, 2024, 2:09 p.m.

Python

9 +0

442 +0

74 +0

GitHub
redun by insitro

Yet another redundant workflow engine

updated at May 17, 2024, 3:09 a.m.

Python

15 +0

489 +0

40 +2

GitHub
bioservices by cokelaer

Access to Biological Web Services from Python.

updated at May 17, 2024, 9:55 p.m.

Python

18 +0

273 +0

61 +0

GitHub
bcbio-nextgen by bcbio

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

updated at May 21, 2024, 1:58 p.m.

Python

87 +0

978 +1

357 +0

GitHub
pyensembl by openvax

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

updated at May 22, 2024, 12:31 p.m.

Python

22 +0

354 +1

66 +0

GitHub