pysradb
ariba
pysradb | ariba | |
---|---|---|
1 | 1 | |
297 | 155 | |
- | 2.6% | |
7.3 | 3.0 | |
8 months ago | 8 months ago | |
Python | Python | |
BSD 3-clause "New" or "Revised" License | GNU General Public License v3.0 or later |
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pysradb
-
Systematic way to collect GEO datasets
If you are okay with looking at already processed data, chdck out https://dee2.io/. Otherwise there is https://github.com/ncbi/sra-tools for getting fastq files (a cli tool) or https://github.com/saketkc/pysradb (python)
ariba
What are some alternatives?
sra-tools - SRA Tools
abricate - :mag_right: :pill: Mass screening of contigs for antimicrobial and virulence genes
kingfisher-download - Easier download/extract of FASTA/Q read data and metadata from the ENA, NCBI, AWS or GCP.
galaxy - Data intensive science for everyone.
GermlineMutationCalling - An adaptable Snakemake workflow which uses GATKs best practice recommendations to perform germline mutation calling starting with BAM files
MGEfinder - A toolbox for identifying mobile genetic element (MGE) insertions from short-read sequencing data of bacterial isolates.
edgecase - A framework for extracting telomeric reads from single-molecule sequencing experiments, describing their sequence variation and motifs, and for haplotype inference.
abritamr - A pipeline for running AMRfinderPlus and collating results into functional classes
16SMaRT - 16s rRNA Sequencing Meta-analysis Reproducibility Tool (using mothur).
hgvs - Python library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`
deepvariant - DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.