Advanced bioinformatic analysis, including analysis for RNA splicing/RNA editing Very competitive price in RNA-seq and Whole Exome Seq Fast turn around time (our NovaSeq runs once a week and Hiseq X or 4000 runs twice a week on a routine basis) ★We have NovaSeq, HiSeqX, Hiseq 4000, two NextSeq500, one MiSeq and one Ion Proton. We also help physicians to unleash the power of NGS in disease diagnosis. We provide NGS service as well as related reagents to investigate the functions of identified variants. with a focus on developing new technologies to allow scientists/physicians to obtain more results in less time. Variant annotation using multiple VCF callers for any pipeline using our annotation algorithm that includes more than 200 genetic mutations databases, Other services offered by Varstation: ServiceĮxome analysis inside Varstation using the gold standard methodologies, including disease and HPO correlation and filtering.Įnd-to-end tool, from the sequencing raw file to the variant reportĬomplete CNV processing from sequencing data to final report using know CNV baseline We provide a Datavis feature to share results with partners. Relevant clinical information to support the medical report, such as patient, variants and therapies info. More than 200 genetic mutations databases are incorporated, including data for germline, somatic and structural variants (CNV and Fusion).įiltering engine based on all annotated mutation data, including human phenotypes, the patient's clinical history and diseases (OMIM / UniProt). We offer a solid bioinformatics foundation for laboratories that want to start or scale their capacity to perform genetic testing while following the best practices from ACMG, AMP and CAP.Įvaluation of quality parameters, mapping, multiple variant callers, database annotation and automatic pre-classification according to ACMG and AMP guidelines. * Somatic mutations - require Tumor-Normal pair (SNVs, INDELs, CNVs, MSI, TMB) * Germline variants, compared to reference genome Exome analysis includes quality control, alignment, variant calling, variant annotation and actionable information (available therapies and clinical trials). We use a neural network-based variant caller for accurate detection of variants in the tumour sample. Other services offered by Cambridge Cancer Genomics: Service Ultimately, we will ensure that each patient has the right treatment, at the right time, to beat their cancer. It provides comprehensive tumour profiling and reports actionable molecular insights to enable the delivery of a personalised treatment strategy for each patient. Our OncOS platform offers data analysis in a rapid, scalable and secure manner. We replicate recommended analysis pipelines (best practice) using open source software.ĬCG has developed precision oncology solutions for robust genomic data analysis. Primer design for efficient multiplex PCR reactions Second, we can help you to set up (cloud) computing solutions that will allow you to run and extend your analyses ind… #BEST FREE BIOINFORMATICS SOFTWARE CLC SEQUENCE VIEWER CODE#We build up your in house bioinformatics capacity in 2 ways: First, we provide you with the code underlying the analysis you requested. We replicate recommended analysis pipelines (best practice) or develop novel ones according to your specifications using open source software. Other services offered by Geno-plex Bioinformatics Services: Service We replicate recommended analysis pipelines (best practice) or develop novel ones but we always emphasize biological interpretation of your data. Second, we can help you to set up (cloud) computing solutions that will allow you to run and extend your analyses independently. We have a strong academic background with a focus on cutting edge, open source software. We offer tailored bioinformatics services (mainly NGS data analysis) to academic and private organizations.
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