Bioinformatic Solutions, LLC

Open-source software

Paralome

A reproducible, checkpointed, HPC-oriented workflow framework for omics analysis — one stage-graph, SLURM-array and checkpoint backbone underneath independent ATAC-seq, RNA-seq, single-cell and variant pipelines.

In active development — public release pending publication

Paralome is used in production for the analyses this laboratory delivers, and is being prepared for public release alongside the manuscript describing it. The source is available to editors and reviewers on request.

01 / Analyses

The analysis name is the verb

CommandData
DNAExome and whole-genome variant calling
RNABulk RNA-seq
ATACBulk ATAC-seq
scRNASingle-cell RNA, whole cell or nuclei
snATACSingle-nuclei ATAC

There is no run subcommand. One command names an analysis and hands it a cohort, and the framework decomposes that into stages, submits them, waits, validates and moves on.

paralome scRNA --rds obj.rds --project A_vs_B \
               --group-by sample,cell_type \
               --control CON:wt --treatment TRT:ko \
               --genome mouse_grcm39 --backend slurm --submit

02 / Design

What the framework guarantees

03 / Citation

How to cite

Jones, K. Paralome: a reproducible, checkpointed workflow framework for omics analysis. Bioinformatic Solutions.

Released under the GNU General Public License v3.0 or later. A citable archived version with a DOI will accompany the public release.

Check before publishing. CITATION.cff in the repository still declares version: 1.0.0 and a July 2026 release date, inherited from the pre-0.1 numbering. That contradicts the version the software reports and should be corrected before a reviewer reads it.