Strand Life Sciences Pvt. Ltd. services
Analysis Services in Bioinformatics
Bioinformatics analysis can be tricky. You may have large-scale RNA-Seq data, and don’t know whether technical effects are relevant; or you may have large grouped cohorts of DNA-Seq data, and need to narrow down your variant list to a few significant ones, associated with disease; or you may want to do an integrated study on a dataset containing RNA and ChIP-Seq samples.
Variant Curation Services
Laboratories running NGS-based clinical tests are challenged with the labor of variant interpretation. To support our clinical diagnostics business, we have built up databases of curated variants across 3 different application areas:
Software Services in Bioinformatics
Since we started in 2000, we have built bioinformatics software for most analytics platforms: microarrays, mass spectrometry, next generation sequencing, high throughput microscopy, and digital PCR. We have covered the spectrum from genomics, transcriptomics, epigenomics to systems biology. We have built high performance software for GPUs, speeded up drug discovery algorithms for pharmaceutical companies many-fold, created Natural Language Processing algorithms for mining protein interactions, and systems biology platforms for predicting drug-induced liver injury.
SmartLab Services
Strand has extensive experience in validating NGS-based panels under CAP- and CLIA-settings: be it germline panels, somatic tumor panels, or liquid biopsy panels, and be it small panels with tens of genes, to large panels with thousands of genes.