CLI bioinformatics tools
Run genomics and metagenomics workflows with aligners, assemblers, taxonomic profilers, gene predictors, format utilities, and related command-line pipelines.
We execute clearly scoped bioinformatics and scientific data-processing workflows when local setup, many files, large datasets, or reproducible reporting become the bottleneck.
Public tools are ideal for quick checks. Custom analysis is for full datasets, repeated runs, custom parameters, and deliverables you can hand to a collaborator.
Run genomics and metagenomics workflows with aligners, assemblers, taxonomic profilers, gene predictors, format utilities, and related command-line pipelines.
Assess sequencing files, tabular outputs, sample metadata, and intermediate results with concise summaries and flags for files needing attention.
Turn tool outputs into clean tables, reports, summaries, figures, or structured files ready for downstream statistics, plotting, and sharing.
Large FASTA/FASTQ filtering, splitting, conversion, ID extraction, summary metrics, and batch processing.
Run, adapt, and document shell, Python, and R scripts for batch processing, reproducible analysis steps, file conversion, and custom summaries.
We focus on execution and structured results. When relevant, deliverables include the commands, versions, parameters, and notes needed to understand how the outputs were produced.
The first step is always scope. Do not send sensitive, clinical, personal, or regulated data before we agree on the task and transfer method.
Send task detailsTell us the data type, number of files, approximate size, desired output, and tools or parameters if known.
We check feasibility, define deliverables, and agree on fixed pricing before files are transferred.
Analyses are executed with documented tools, parameters, and data-handling expectations.
You receive the agreed result files, tables, reports, and execution notes.
Send the task, input format, approximate size, number of files, and expected output.