Meet us at ASHG 2015!
We are excited to be a part of the Annual Meeting of The American Society of Human Genetics (ASHG) again, this time in Baltimore, Maryland from 6- 10 October 2015. Come and meet us to learn more about...
View ArticleWebinar on Strand NGS Pipeline Manager for streamlining large scale analysis
This webinar, will highlight the Strand NGS Pipeline Manager feature. In this webinar, you will learn how to customize pipelines and share them with other Strand NGS users. This webinar will give a...
View ArticleReview of selected publications citing Strand NGS
In 2015, we brought in many new features and improvements based on your requirements and feedback. We expanded the Strand NGS epigenomics toolkit by adding the MeDIP-Seq workflow in the v2.5 release....
View ArticleStrand NGS v2.7 released
We are excited to share the release of Strand NGS v2.7. This new version comes with several exciting features and enhancements. Listed below are few major enhancements: Strand NGS v2.7 is upgraded to...
View ArticleReduce the SNP annotation time by up to 95%
Explore the new script ‘Create Targeted VAL’ in Strand NGS for creating subset of dbSNP database with target regions of interest and run your analysis. This feature reduces your SNP annotation time by...
View ArticleCelebrating 25th Release announcement of Strand NGS
We are happy to share the announcement of the 25th release of Strand NGS (v2.8). We started our journey as bioinformatics experts in 2000, and moved into the next-generation sequencing space with the...
View ArticleWebinar on Implications of Next Generation Sequencing in Molecular Diagnosis...
Genetic testing requires screening of the entire gene, which by conventional sequencing is time consuming and expensive. Next Generation Sequencing (NGS) based approaches increase the sensitivity of...
View ArticleWebinar on RNA-Seq Data Analysis
Strand NGS supports an extensive workflow for the analysis and visualization of RNA-Seq data. The workflow includes Transcriptome / Genome alignment, Differential expression analysis with Statistical...
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The clinical workflow, retinoblastoma and split alignment
An infant with leukocoria, a common retinoblastoma symptom visible in photographs taken with a camera flash. The normal right eye reflects red, as it should; the left eye, infected, reflects white....
View ArticleIntegrated mRNA and microRNA transcriptome analysis in Strand NGS
Using a nasopharyngeal carcinoma case study, this paper highlights the integrated transcriptome analysis capabilities of Strand NGS demonstrating the identification of miRNA – mRNA interactions in...
View ArticleIntegrative RNA and ChIP-Seq analysis of regulatory T-cells
Integrative RNA and ChIP-Seq analysis of regulatory T-cells , a Strand NGS application note describes how integrated multi-omics functionality in Strand NGS was used to find the regulatory role of...
View ArticleWebinar on Implications of Next Generation Sequencing in Molecular Diagnosis...
Genetic testing requires screening of the entire gene, which by conventional sequencing is time consuming and expensive. Next Generation Sequencing (NGS) based approaches increase the sensitivity of...
View ArticleWebinar on RNA-Seq Data Analysis
Strand NGS supports an extensive workflow for the analysis and visualization of RNA-Seq data. The workflow includes Transcriptome / Genome alignment, Differential expression analysis with Statistical...
View ArticleWebinar on Unravelling complex mutational events in clinical cases using the...
Live webinar on Unravelling complex mutational events in clinical cases using the power of Next generation sequencing data analysis by Dr Satish Sankaran on 31 Jan 2018 at 9am CET and 8am PST Speaker:...
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Ultra-sensitive variant calling and transcript quantification using Unique...
Background Next Generation Sequencing (NGS) technologies have remarkably revolutionized the medical and genomics research. The incremental cost reductions and size of the throughput at molecular...
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What’s new in Strand NGS 3.4
Data quality is of utmost importance for accurate and valid downstream NGS analysis. Sequence artifacts contribute to erroneous interpretations in analysis. Focusing on this, we have introduced two...
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The silent biomarkers of stem cells- Small RNA
I was watching this movie, where the protagonists were a race of human clones made from “stem cells” and they try to defend their lives from the native human race. You might have already heard of dolly...
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