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Genome Analysis Python Packages

Python packages with the GitHub topic genome-analysis. Sorted by relevance, with stars and monthly downloads.
biocommons
bioutils

provides common tools and lookup tables used primarily by the hgvs and uta packages

94K 25 20
biocommons
biocommons-seqrepo

non-redundant, compressed, journalled, file-based storage for biological sequences

86K 50 36
biocommons
hgvs

Python library to parse, format, validate, normalize, and map sequence variants according to HGVS Nomenclature (https://hgvs-nomenclature.org/).

76K 287 97
akikuno
dajin2

🔬 Genotyping tool for genome-edited samples using nanopore-targeted sequencing

6K 14 0
populationgenomics
cpg-workflows

Genomics workflows for CPG using Hail Batch

6K 12 2
OmerKerner
nolzss

Non-overlapping Lempel–Ziv–Storer–Szymanski Factorization Python Library

2K 2 0
michaelgruenstaeudl
plastburstalign

A Python tool to extract and align genes, introns, and intergenic spacers across hundreds of plastid genomes using associative arrays

2K 1 0
moshi4
cogclassifier

A tool for classifying prokaryote protein sequences into COG(Cluster of Orthologous Genes) functional category

1K 83 6
pyani-plus
pyani-plus

Development repo for pyani-plus (the next iteration of pyani)

774 33 2
biocommons
seqrepo

non-redundant, compressed, journalled, file-based storage for biological sequences

746 50 36
DoubleHelixApp
doublehelix

Genomic data manipulation tool

704 6 0
WGLab
nanorepeat

NanoRepeat: fast and accurate analysis of Short Tandem Repeats (STRs) from Oxford Nanopore sequencing data

699 19 4
SouradiptoC
codonu

An integrated package for codon usage analysis

606 25 1
kishwarshafin
helen

H.E.L.E.N. (Homopolymer Encoded Long-read Error-corrector for Nanopore)

549 73 12
omatheuspimenta
gramep

GRAMEP - Genome vaRiation Analysis from the Maximum Entropy Principle

445 7 2
asntech
intervene

Intervene: a tool for intersection and visualization of multiple genomic region and gene sets

433 147 32
biocommons
biocommons-anyvar

Lightweight, portable variation registration and retrieval

277 16 6
biocommons
anyvar

AnyVar provides Python and REST interfaces to validate, normalize, generate identifiers, and register biological sequence variation according to the GA4GH Variation Representation standards.

260 16 6
MiraldiLab
maxatac

Transcription Factor Binding Prediction from ATAC-seq and scATAC-seq with Deep Neural Networks

136 30 11
AminMahpour
wigman

Generate heatmap plots from genomic BigWig data

128 2 0
GenomeHouse
genomehouse

Modular bioinformatics toolkit for sequence analysis, genomic data parsing, machine learning, and visualization all in one package.

118 0 0
biocommons
seqrepo-rest-service

OpenAPI-based REST interface to biological sequences and sequence metadata

114 6 6
latur
makegms

Genome mappability estimation tool

45 0 0
    • Data from PyPI, GitHub, ClickHouse, and BigQuery