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FASTQ to Analysis-Ready Files

Here you will find the current list of BioFigR services focused on transforming raw sequencing reads into usable data.

No two projects are exactly alike.

 

If your requirements fall outside the services listed below, get in touch to discuss your objectives and explore how BioFigR can support your analysis needs.

Short-Read Services

Human

WGS

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Identify mutations and variants in solo or paired human whole genome sequencing data.

DETAILS

CUT&RUN / CUT&Tag

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High-precision mapping of protein-DNA binding sites using CUT&RUN and CUT&Tag.

DETAILS

Mitochondrial

DNA Assembly

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Assemble and analyse mitochondrial genomes from short-read sequencing data.

DETAILS

eDNA Metabarcoding

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Characterise micro- or macrobiology composition using amplicon marker genes. 

DETAILS

Bulk

RNA-seq

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Quantify gene expression across whole transcriptomes using bulk RNA-seq data.

DETAILS

Viral Metagenomics

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Identify known and unknown viral sequences from shotgun or viral-enriched metagenomic data.

DETAILS

Supplementary Info

Socials 

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