Webinar on Streamlining large scale analysis using the Strand NGS Pipeline Manager on 24 Feb 2016
...ining large scale NGS data analysis using the Strand NGS Pipeline Manager on 24 Feb 2016 Abstract: Strand NGS includes comprehensive workflows for DNA-Seq, RNA-Seq, Small RNA-Seq,...3005 days ago
2903 days ago
Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017
Continuing our DNA-Seq webinar series, we'll present Strand NGS v3.0 best-practices: a workflow that identifies highly accurate variants from raw reads. Our best practices...2564 days ago
2468 days ago
Strand Life Sciences announces the release of Strand NGS v3.1 at ASHG 2017
...Seq and Unique Molecular Identifiers (UMIs) for DNA-, RNA-, and small-RNA-Seq. S...for Unique Molecular Identifiers, or UMIs, for DNA-, RNA- and small-RNA-Seq. UMI...sies and low-grade FFPE samples, UMI support in DNA-Seq enables the detection of...2379 days ago
2364 days ago
SCFBio have developed Sanjeevini
...he easy to use in-built module "Prepare protein/DNA".SCFBio have worked towa...dule name Activity 1 Prepare Protein/DNA Prepares protein/DNA for oth...protein 14 Intercalate Rigid Docking of DNA-Ligand complex in intercalati...2354 days ago
1mb long DNA with Nanopore technology
The first continuous DNA read of more than a million bases (>1Mb) has been achieved, using Oxford Nanopore sequencing technology. Congratulations to Martin Smith and collaborators! Read more: http://bit.ly/2j5TNCO2321 days ago
2195 days ago
You can't hide from Genome Hackers
...Paper: http://science.sciencemag.org/content/early/2018/10/10/science.aau4832 More at https://www.wired.com/story/genome-hackers-show-no-ones-dna-is-anonymous-anymore/2023 days ago